Note: Descriptions are shown in the official language in which they were submitted.
CA 02893598 2015-06-05
CANOLA HYBRID PV 200 CL
FIELD
The invention is in the field of Brassica napus breeding (i.e., canola
.. breeding), specifically relating to the canola variety designated PV 200
CL.
BACKGROUND
The present invention relates to a novel rapeseed variety designated PV
200 CL which is the result of years of careful breeding and selection. Since
such
to variety is of high quality and possesses a relatively low level of
erucic acid in the
vegetable oil component and a relatively low level of glucosinolate content in
the
meal component, it can be termed "canola" in accordance with the terminology
commonly used by plant scientists.
The goal of plant breeding is to combine in a single variety or hybrid various
.. desirable traits. For field crops, these traits may include resistance to
diseases
and insects, tolerance to heat and drought, reducing the time to crop
maturity,
greater yield, and better agronomic quality. With mechanical harvesting of
many
crops, uniformity of plant characteristics such as germination and stand
establishment, growth rate, maturity, and plant and pod height, is important.
The
creation of new superior, agronomically sound, and stable high-yielding
cultivars of
many plant types including canola has posed an ongoing challenge to plant
breeders. Therefore, there is a continuing need in the field of agriculture
for
canola plants having desirable agronomic and industrial characteristics.
SUMMARY
A novel Brassica napus variety designated PV 200 CL is provided. This
invention thus relates to the seeds of the PV 200 CL variety, to plants of the
PV
200 CL variety, and to methods for producing a canola plant by crossing the PV
200 CL variety with itself or another Ganda plant (whether by use of male
sterility
or open pollination), and to methods for producing a canola plant containing
in its
genetic material one or more transgenes, and to transgenic plants produced by
that method. This invention also relates to canola seeds and plants produced
by
crossing the variety PV 200 CL with another line.
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DEFINITIONS
In the description and tables which follow, a number of terms are used. In
order to aid in a clear and consistent understanding of the specification, the
following definitions and evaluation criteria are provided.
Anther Fertility. The ability of a plant to produce pollen; measured by pollen
production. 1 = sterile, 9 = all anthers shedding pollen (vs. Pollen Formation
which is amount of pollen produced).
Anther Arrangement. The general disposition of the anthers in typical fully
opened flowers is observed_
Chlorophyll Content. The typical chlorophyll content of the mature seeds is
determined by using methods recommended by the Western Canada
Canola/Rapeseed Recommending Committee (WCC/RRC). 1 = low (less than 8
ppm), 2 = medium (8 to 15 ppm), 3 = high (greater than 15 ppm). Also,
chlorophyll
could be analyzed using NIR (Near Infrared) spectroscopy as long as the
is instrument is calibrated according to the manufacturer's specifications.
CMS. Abbreviation for cytoplasmic male sterility.
Cotyledon. A cotyledon is a part of the embryo within the seed of a plant; it
is also referred to as a seed leaf. Upon germination, the cotyledon may become
the embryonic first leaf of a seedling.
Cotyledon Length. The distance between the indentation at the top of the
cotyledon and the point where the width of the petiole is approximately 4 mm.
Cotyledon Width. The width at the widest point of the cotyledon when the
plant is at the two to three-leaf stage of development. 3 = narrow, 5 =
medium, 7
= wide.
CV%: Abbreviation for coefficient of variation.
Disease Resistance: Resistance to various diseases is evaluated and is
expressed on a scale of 0 = not tested, 1 = resistant, 3 = moderately
resistant, 5 =
moderately susceptible, 7 = susceptible, and 9 = highly susceptible.
Erucic Acid Content: The percentage of the fatty acids in the form of
C22:1.as determined by one of the methods recommended by the WCC/RRC,
being AOCS Official Method Ce 2-66 Preparation of Methyl esters of Long-Chain
Fatty Acids or AOCS Official Method Ce 1-66 Fatty Acid Composition by Gas
Chromatography.
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Fatty Acid Content: The typical percentages by weight of fatty acids
present in the endogenously formed oil of the mature whole dried seeds are
determined. During such determination the seeds are crushed and are extracted
as fatty acid methyl esters following reaction with methanol and sodium
.. methoxide. Next the resulting ester is analyzed for fatty acid content by
gas liquid
chromatography using a capillary column which allows separation on the basis
of
the degree of unsaturation and fatty acid chain length. This procedure is
described in the work of Daun, et al., (1983) J. Amer. Oil Chem. Soc. 60:1751
to
1754.
Flower Bud Location. A determination is made whether typical buds are
disposed above or below the most recently opened flowers.
Flower Date 50%. (Same as Time to Flowering) The number of days from
planting until 50% of the plants in a planted area have at least one open
flower.
Flower Petal Coloration. The coloration of open exposed petals on the first
is day of flowering is observed.
Frost Tolerance (Spring Type Only). The ability of young plants to
withstand late spring frosts at a typical growing area is evaluated and is
expressed
on a scale of 1 (poor) to 5 (excellent).
Gene Silencing. The interruption or suppression of the expression of a
gene at the level of transcription or translation.
Genotype. Refers to the genetic constitution of a cell or organism.
Glucosinolate Content. The total glucosinolates of seed at 8.5% moisture,
as measured by AOCS Official Method AK-1-92 (determination of glucosinolates
content in rapeseed ¨colza by HPLC), is expressed as micromoles per gram of
defatted, oil-free meal. Capillary gas chromatography of the trimethylsityl
derivatives of extracted and purified desulfoglucosinolates with optimization
to
obtain optimum indole glucosinolate detection is described in "Procedures of
the
Western Canada Canola/Rapeseed Recommending Committee Incorporated for
the Evaluation and Recommendation for Registration of Canola/Rapeseed
Candidate Cultivars in Western Canada". Also, glucosinolates could be analyzed
using NIR (Near Infrared) spectroscopy as long as the instrument is calibrated
according to the manufacturer's specifications.
Grain. Seed produced by the plant or a self or sib of the plant that is
intended for food or feed use.
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Green Seed. The number of seeds that are distinctly green throughout as
defined by the Canadian Grain Commission. Expressed as a percentage of seeds
tested.
Herbicide Resistance: Resistance to various herbicides when applied at
standard recommended application rates is expressed on a scale of 1
(resistant),
2 (tolerant), or 3 (susceptible).
Leaf Anthocyanin Coloration. The presence or absence of leaf anthocyanin
coloration, and the degree thereof if present, are observed when the plant has
reached the 9- to 11-leaf stage.
Leaf Attachment to Stem. The presence or absence of clasping where the
leaf attaches to the stem, and when present the degree thereof, are observed.
Leaf Attitude. The disposition of typical leaves with respect to the petiole
is
observed when at least 6 leaves of the plant are formed.
Leaf Color. The leaf blade coloration is observed when at least six leaves
of the plant are completely developed.
Leaf Glaucosity. The presence or absence of a fine whitish powdery
coating on the surface of the leaves, and the degree thereof when present, are
observed.
Leaf Length. The length of the leaf blades and petioles are observed when
at least six leaves of the plant are completely developed.
Leaf Lobes. The fully developed upper stem leaves are observed for the
presence or absence of leaf lobes when at least 6 leaves of the plant are
completely developed.
Leaf Margin Indentation. A rating of the depth of the indentations along the
upper third of the margin of the largest leaf. 1 = absent or very weak (very
shallow), 3 = weak (shallow), 5 = medium, 7 = strong (deep), 9 = very strong
(very
deep).
Leaf Margin Hairiness. The leaf margins of the first leaf are observed for
the presence or absence of pubescence, and the degree thereof, when the plant
is
at the two leaf-stage.
Leaf Margin Shape. A visual rating of the indentations along the upper third
of the margin of the largest leaf. 1 = undulating, 2 = rounded, 3 = sharp.
Leaf Surface. The leaf surface is observed for the presence or absence of
wrinkles when at least six leaves of the plant are completely developed.
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Leaf Tip Reflexion. The presence or absence of bending of typical leaf tips
and the degree thereof, if present, are observed at the six to eleven leaf-
stage.
Leaf Upper Side Hairiness. The upper surfaces of the leaves are observed
for the presence or absence of hairiness, and the degree thereof if present,
when
at least six leaves of the plant are formed.
Leaf Width. The width of the leaf blades is observed when at least six
leaves of the plant are completely developed.
Locus. A specific location on a chromosome.
Locus Conversion. A locus conversion refers to plants within a variety that
io have been modified in a manner that retains the overall genetics of the
variety and
further comprises one or more loci with a specific desired trait, such as male
sterility, insect, disease or herbicide resistance. Examples of single locus
conversions include mutant genes, transgenes and native traits finely mapped
to a
single locus. One or more locus conversion traits may be introduced into a
single
is canola variety.
Lodging Resistance. Resistance to lodging at maturity is observed. 1 = not
tested, 3 = poor, 5 = fair, 7 = good, 9 = excellent.
LSD. Abbreviation for least significant difference.
Maturity. The number of days from planting to maturity is observed, with
20 maturity being defined as the plant stage when pods with seed change color,
occurring from green to brown or black, on the bottom third of the pod-bearing
area of the main stem.
NMS. Abbreviation for nuclear male sterility.
Number of Leaf Lobes. The frequency of leaf lobes, when present, is
25 observed when at least six leaves of the plant are completely developed.
Oil Content: The typical percentage by weight oil present in the mature
whole dried seeds is determined by ISO 10565:1993 Oilseeds Simultaneous
determination of oil and water - Pulsed NMR method. Also, oil could be
analyzed
using NIR (Near Infrared) spectroscopy as long as the instrument is calibrated
30 according to the manufacturer's specifications, reference AOCS Procedure
Am 1-
92 Determination of Oil, Moisture and Volatile Matter, and Protein by Near-
Infrared
Reflectance.
Pedicel Length. The typical length of the silique stem when mature is
observed. 3 = short, 5 = medium, 7 = long.
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Petal Length. The lengths of typical petals of fully opened flowers are
observed. 3 = short, 5 = medium, 7 = long.
Petal Width. The widths of typical petals of fully opened flowers are
observed. 3 = short, 5 = medium, 7 = long.
Petiole Length. The length of the petioles is observed, in a line forming
lobed leaves, when at least six leaves of the plant are completely developed.
3 =
short, 5 = medium, 7 = long.
Plant Height. The overall plant height at the end of flowering is observed.
3 = short, 5 = medium, 7 = tall.
I() Ploidy. This refers to the number of chromosomes exhibited by the line,
for
example diploid or tetraploid.
Pod Anthocyanin Coloration. The presence or absence at maturity of
silique anthocyanin coloration, and the degree thereof if present, are
observed.
Pod (Silique) Beak Length. The typical length of the silique beak when
is mature is observed. 3 = short, 5 = medium, 7 = long.
Pod Habit. The typical manner in which the siliques are borne on the plant
at maturity is observed.
Pod (Silique) Length. The typical silique length is observed. 1 = short (less
than 7 cm), 5 = medium (7 to 10 cm), 9 = long (greater than 10 cm).
20 Pod (Silique) Attitude. A visual rating of the angle joining the pedicel
to the
pod at maturity. 1 = erect, 3 = semi-erect, 5 = horizontal, 7 = semi-drooping,
9 =
drooping.
Pod Type. The overall configuration of the silique is observed.
Pod (Silique) Width. The typical pod width when mature is observed. 3 =
25 narrow (3 mm), 5 = medium (4 mm), 7 = wide (5 mm).
Pollen Formation. The relative level of pollen formation is observed at the
time of dehiscence.
Protein Content: The typical percentage by weight of protein in the oil free
meal of the mature whole dried seeds is determined by AOCS Official Method Ba
30 4e-93 Combustion Method for the Determination of Crude Protein. Also,
protein
could be analyzed using NIR (Near Infrared) spectroscopy as long as the
instrument is calibrated according to the manufacturer's specifications,
reference
AOCS Procedure Am 1-92 Determination of Oil, Moisture and Volatile Matter, and
Protein by Near-Infrared Reflectance.
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Resistance. The ability of a plant to withstand exposure to an insect,
disease, herbicide, or other condition. A resistant plant variety or hybrid
will have
a level of resistance higher than a comparable wild-type variety or hybrid.
"Tolerance" is a term commonly used in crops such as canola, soybean, and
.. sunflower affected by an insect, disease, such as Sclerotinia, herbicide,
or other
condition and is used to describe an improved level of field resistance.
Root Anthocyanin Coloration. The presence or absence of anthocyanin
coloration in the skin at the top of the root is observed when the plant has
reached
at least the six- leaf stage.
Root Anthocyanin Expression. When anthocyanin coloration is present in
skin at the top of the root, it further is observed for the exhibition of a
reddish or
bluish cast within such coloration when the plant has reached at least the six-
leaf
stage.
Root Anthocyanin Streaking. When anthocyanin coloration is present in the
is skin at the top of the root, it further is observed for the presence or
absence of
streaking within such coloration when the plant has reached at least the six-
leaf
stage.
Root Chlorophyll Coloration. The presence or absence of chlorophyll
coloration in the skin at the top of the root is observed when the plant has
reached
at least the six-leaf stage.
Root Coloration Below Ground. The coloration of the root skin below
ground is observed when the plant has reached at least the six-leaf stage.
Root Depth in Soil. The typical root depth is observed when the plant has
reached at least the six-leaf stage.
Root Flesh Coloration. The internal coloration of the root flesh is observed
when the plant has reached at least the six-leaf stage.
SE. Abbreviation for standard error.
Seedling Growth Habit. The growth habit of young seedlings is observed
for the presence of a weak or strong rosette character. 1 = weak rosette, 9 =
strong rosette.
Seeds Per Pod. The average number of seeds per pod is observed.
Seed Coat Color. The seed coat color of typical mature seeds is observed.
1 = black, 2 = brown, 3 = tan, 4 = yellow, 5 = mixed, 6 = other.
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Seed Coat Mucilage. The presence or absence of mucilage on the seed
coat is determined and is expressed on a scale of 1 (absent) to 9 (present).
During such determination a petri dish is filled to a depth of 0.3 cm. with
water
provided at room temperature. Seeds are added to the petri dish and are
immersed in water where they are allowed to stand for five minutes. The
contents
of the petri dish containing the immersed seeds are then examined under a
stereo
microscope equipped with transmitted light. The presence of mucilage and the
level thereof is observed as the intensity of a halo surrounding each seed.
Seed Size. The weight in grams of 1,000 typical seeds is determined at
to maturity while such seeds exhibit a moisture content of approximately 5 to
6
percent by weight.
Shatter Resistance. Resistance to silique shattering is observed at seed
maturity. 1 = not tested, 3 = poor, 5 = fair, 7 = good, 9 = does not shatter.
Si. Abbreviation for self-incompatible.
Speed of Root Formation. The typical speed of root formation is observed
when the plant has reached the four to eleven-leaf stage.
SSFS. Abbreviation for Sclerotinia sclerotiorum Field Severity score, a
rating based on both percentage infection and disease severity.
Stem Anthocyanin Intensity. The presence or absence of leaf anthocyanin
coloration and the intensity thereof, if present, are observed when the plant
has
reached the nine to eleven-leaf stage. 1 = absent or very weak, 3 = weak, 5 =
medium, 7 = strong, 9 = very strong.
Stem Lodging at Maturity. A visual rating of a plant's ability to resist stem
lodging at maturity. 1 = very weak (lodged), 9 = very strong (erect).
Time to Flowering. A determination is made of the number of days when at
least 50 percent of the plants have one or more open buds on a terminal raceme
in the year of sowing.
Seasonal Type. This refers to whether the new line is considered to be
primarily a Spring or Winter type of canola.
Winter Survival (Winter Type Only). The ability to withstand winter
temperatures at a typical growing area is evaluated and is expressed on a
scale of
1 (poor) to 5 (excellent).
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This invention relates to:
<1> A plant cell from canola variety PV 200 CL, wherein
representative seed of
said variety has been deposited under ATCC accession number PTA-
122193.
<2> The plant cell of <1> wherein the plant cell is a seed cell.
<3> A locus converted plant cell of a locus converted plant obtained
by
introducing a locus conversion into canola variety PV 200 CL wherein
representative seed of said variety has been deposited under ATCC
Accession Number PTA-122193, and wherein the locus converted plant
cell is the same as the cell from variety PV 200 CL except for the locus
conversion and the locus converted plant otherwise expresses the
physiological and morphological characteristics of canola variety PV 200
CL listed in Table 1 as determined at the 5% significance level grown
under substantially similar environmental conditions.
<4> The plant cell of <3>, wherein the locus conversion confers a
trait and the
trait is: male sterility, site-specific recombination, abiotic stress
tolerance,
altered phosphate, altered antioxidants, altered fatty acids, altered
essential amino acids, altered carbohydrates, herbicide resistance, insect
resistance or disease resistance.
<5> Use of a canola plant of canola variety PV 200 CL, representative
seed of
said variety having been deposited under ATCC accession number PTA-
122193 to breed a second plant.
<6> Use of a canola plant of canola variety PV 200 CL, representative
seed of
said variety having been deposited under ATCC accession number PTA-
122193 to breed an inbred.
<7> The use of <6>, wherein the canola plant is used to produce a
haploid that
is subsequently doubled to produce a double haploid inbred.
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<8> Use of a canola seed of canola variety PV 200 CL, representative
seed of
said variety having been deposited under ATCC accession number PTA-
122193 to produce clean seed.
<9> A canola seed cell of canola variety PV 200 CL, representative
seed of
said variety having been deposited under ATCC accession number PTA-
122193, wherein the seed is clean seed.
<10> Use of a canola seed of canola variety PV 200 CL, representative seed of
said variety having been deposited under ATCC accession number PTA-
122193 to produce treated seed.
<11> The use of <10> wherein the seed is treated with fungicide or pesticide.
<12> A canola seed cell of canola variety PV 200 CL, representative seed of
said variety having been deposited under ATCC accession number PTA-
122193, wherein the seed is a treated seed.
<13> Use of a canola seed of canola variety PV 200 CL, representative seed of
said variety having been deposited under ATCC accession number PTA-
122193 to grow subsequent generations.
<14> Use of a collection of seed from a commercial bag of canola hybrid
variety
PV 200 CL, representative seed of said variety having been deposited
under ATCC accession number PTA-122193, for screening for
contaminating canola inbred varieties NS6513 or NS7364.
<15> Use of a canola hybrid plant designated PV 200 CL, seed of said hybrid
having been deposited under ATCC accession number PTA-122193, to
produce F2 seed.
<16> Use of an Fl hybrid canola plant designated PV 200 CL, seed of said
hybrid having been deposited under ATCC accession number PTA-
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122193 to produce a commodity product comprising seed oil, meal, fibre or
protein.
<17> The use of <16>, wherein the commodity product comprises seed oil.
<18> Use of a canola hybrid plant designated PV 200 CL, seed of said hybrid
having been deposited under ATCC accession number PTA-122193, to
produce crushed non-viable F2 seed.
<19> The use of <18> wherein the crushed non-viable F2 seed is for use in the
production of seed oil, meal, fibre or protein.
<20> Use of a canola seed of canola variety PV 200 CL, representative seed of
said variety having been deposited under ATCC accession number PTA-
122193 as a recipient of a locus conversion.
<21> Use of canola variety PV 200 CL, representative seed of said variety
having been deposited under ATCC accession number PTA-122193, as a
crop.
<22> Use of canola variety PV 200 CL, representative seed of said variety
having been deposited under ATCC accession number PTA-122193, as a
source of propagating material.
<23> The use of <22>, wherein the propagating material is a seed.
<24> The use of <19>, wherein the seed oil, meal, fiber or protein is for
consumption.
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DETAILED DESCRIPTION
Field crops are bred through techniques that take advantage of the plant's
method of pollination. A plant is self-pollinated if pollen from one flower is
transferred to the same or another flower of the same plant or a genetically
identical plant. A plant is sib-pollinated when individuals within the same
family or
line are used for pollination. A plant is cross-pollinated if the pollen comes
from a
flower on a genetically different plant from a different family or line. The
term
"cross-pollination" used herein does not include self-pollination or sib-
pollination.
In the practical application of a chosen breeding program, the breeder often
io initially selects and crosses two or more parental lines, followed by
repeated
selfing and selection, thereby producing many unique genetic combinations. The
breeder can theoretically generate billions of different genetic combinations
via
crossing, selfing and mutagenesis.
In each cycle of evaluation, the plant breeder selects the germplasm to
is advance to the next generation. This germplasm is grown under chosen
geographical, climatic and soil conditions, and further selections are then
made
during and at the end of the growing season. The characteristics of the
varieties
developed are incapable of prediction in advance.
Canola breeding programs utilize techniques such as mass and recurrent
20 selection, backcrossing, pedigree breeding and haploidy. For a
general
description of rapeseed and Canola breeding, see, Downey and Rakow, (1987)
"Rapeseed and Mustard" In: Principles of Cultivar Development, Fehr, (ed.), pp
437-486; New York; Macmillan and Co.; Thompson, (1983) "Breeding winter
oilseed rape Brassica napus''; Advances in Applied Biology 7:1-104; and Ward,
et.
25 al., (1985) Oilseed Rape, Farming Press Ltd., Wharfedale Road, Ipswich,
Suffolk.
Recurrent selection is used to improve populations of either self- or cross-
pollinating Brassica. Through recurrent selection, a genetically variable
population
of heterozygous individuals is created by intercrossing several different
parents.
The best plants are selected based on individual superiority, outstanding
progeny,
30 and/or excellent combining ability. The selected plants are intercrossed
to
produce a new population in which further cycles of selection are continued.
Various recurrent selection techniques are used to improve quantitatively
inherited
traits controlled by numerous genes.
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Breeding programs use backcross breeding to transfer genes for a simply
inherited, highly heritable trait into another line that serves as the
recurrent parent.
The source of the trait to be transferred is called the donor parent. After
the initial
cross, individual plants possessing the desired trait of the donor parent are
selected and are crossed (backcrossed) to the recurrent parent for several
generations. The resulting plant is expected to have the attributes of the
recurrent
parent and the desirable trait transferred from the donor parent. This
approach
has been used for breeding disease resistant phenotypes of many plant species,
and has been used to transfer low erucic acid and low glucosinolate content
into
io lines and breeding populations of Brassica.
Pedigree breeding and recurrent selection breeding methods are used to
develop varieties from breeding populations. Pedigree breeding starts with the
crossing of two genotypes, each of which may have one or more desirable
characteristics that is lacking in the other or which complements the other.
If the
two original parents do not provide all of the desired characteristics, other
sources
can be included in the breeding population. In the pedigree method, superior
plants are selfed and selected in successive generations. In the succeeding
generations the heterozygous condition gives way to homogeneous lines as a
result of self-pollination and selection. Typically in the pedigree method of
breeding, five or more generations of selfing and selection are practiced: F1
to F2;
F2 to F3; F3 to F4; F4 to F5, etc. For example, two parents that are believed
to
possess favorable complementary traits are crossed to produce an F1. An F2
population is produced by selfing one or several Fi's or by intercrossing two
F1's
(i.e., sib mating). Selection of the best individuals may begin in the F2
population,
and beginning in the F3 the best individuals in the best families are
selected.
Replicated testing of families can begin in the F4 generation to improve the
effectiveness of selection for traits with low heritability. At an advanced
stage of
inbreeding (i.e., F6 and F7), the best lines or mixtures of phenotypically
similar
lines commonly are tested for potential release as new cultivars. Backcrossing
may be used in conjunction with pedigree breeding; for example, a combination
of
backcrossing and pedigree breeding with recurrent selection has been used to
incorporate blackleg resistance into certain cultivars of Brassica napus.
Plants that have been self-pollinated and selected for type for many
generations become homozygous at almost all gene loci and produce a uniform
CA 02893598 2015-06-05
population of true breeding progeny. If desired, double-haploid methods can
also
be used to extract homogeneous lines. A cross between two different
homozygous lines produces a uniform population of hybrid plants that may be
heterozygous for many gene loci. A cross of two plants each heterozygous at a
number of gene loci will produce a population of hybrid plants that differ
genetically and will not be uniform.
The choice of breeding or selection methods depends on the mode of plant
reproduction, the heritability of the trait(s) being improved, and the type of
cultivar
used commercially, such as F1 hybrid variety or open pollinated variety. A
true
io breeding
homozygous line can also be used as a parental line (inbred line) in a
commercial hybrid. If the line is being developed as an inbred for use in a
hybrid,
an appropriate pollination control system should be incorporated in the line.
Suitability of an inbred line in a hybrid combination will depend upon the
combining
ability (general combining ability or specific combining ability) of the
inbred.
Various breeding procedures are also utilized with these breeding and
selection methods. The single-seed descent procedure in the strict sense
refers
to planting a segregating population, harvesting a sample of one seed per
plant,
and using the one-seed sample to plant the next generation. When the
population
has been advanced from the F2 to the desired level of inbreeding, the plants
from
which lines are derived will each trace to different F2 individuals. The
number of
plants in a population declines each generation due to failure of some seeds
to
germinate or some plants to produce at least one seed. As a result, not all of
the
F2 plants originally sampled in the population will be represented by a
progeny
when generation advance is completed.
In a multiple-seed procedure, canola breeders commonly harvest one or
more pods from each plant in a population and thresh them together to form a
bulk. Part of the bulk is used to plant the next generation and part is put in
reserve. The procedure has been referred to as modified single-seed descent or
the pod-bulk technique. The multiple-seed procedure has been used to save
labor
at harvest. It is considerably faster to thresh pods with a machine than to
remove
one seed from each by hand for the single-seed procedure. The multiple-seed
procedure also makes it possible to plant the same number of seeds of a
population each generation of inbreeding. Enough seeds are harvested to make
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up for those plants that did not germinate or produce seed. If desired,
doubled-
haploid methods can be used to extract homogeneous lines.
Molecular markers, including techniques such as Isozyme Electrophoresis,
Restriction Fragment Length Polymorphisms (RFLPs), Randomly Amplified
Polymorphic DNAs (RAPDs), Arbitrarily Primed Polymerase Chain Reaction (AP-
PC R), DNA Amplification Fingerprinting (DAF), Sequence Characterized
Amplified
Regions (SCARs), Amplified Fragment Length Polymorphisms (AFLPs), Simple
Sequence Repeats (SSRs) and Single Nucleotide Polymorphisms (SNPs), may be
used in plant breeding methods. One use of molecular markers is Quantitative
to Trait Loci (QTL) mapping. QTL mapping is the use of markers which are
known to
be closely linked to alleles that have measurable effects on a quantitative
trait.
Selection in the breeding process is based upon the accumulation of markers
linked to the positive effecting alleles and/or the elimination of the markers
linked
to the negative effecting alleles in the plant's genome.
Is Molecular markers can also be used during the breeding process for
the
selection of qualitative traits. For example, markers closely linked to
alleles or
markers containing sequences within the actual alleles of interest can be used
to
select plants that contain the alleles of interest during a backcrossing
breeding
program. The markers can also be used to select for the genome of the
recurrent
20 parent and against the markers of the donor parent. Using this procedure
can
minimize the amount of genome from the donor parent that remains in the
selected plants. It can also be used to reduce the number of crosses back to
the
recurrent parent needed in a backcrossing program. The use of molecular
markers in the selection process is often called Genetic Marker Enhanced
25 Selection or Marker Assisted Selection (MAS).
The production of doubled haploids can also be used for the development
of inbreds in the breeding program. In Brassica napus, microspore culture
technique is used in producing haploid embryos. The haploid embryos are then
regenerated on appropriate media as haploid plantlets, doubling chromosomes of
30 which results in doubled haploid plants. This can be advantageous because
the
process omits the generations of selfing needed to obtain a homozygous plant
from a heterozygous source.
The development of a canola hybrid in a canola plant breeding program
involves three steps: (1) the selection of plants from various germplasm pools
for
12
CA 02893598 2015-06-05
initial breeding crosses; (2) the selfing of the selected plants from the
breeding
crosses for several generations to produce a series of inbred lines, which,
although different from each other, breed true and are highly uniform; and (3)
crossing the selected inbred lines with different inbred lines to produce the
hybrids. During the inbreeding process in canola, the vigor of the lines
decreases.
Vigor is restored when two different inbred lines are crossed to produce the
hybrid.
An important consequence of the homozygosity and homogeneity of the inbred
lines is that the hybrid between a defined pair of inbreds will always be the
same.
Once the inbreds that give a superior hybrid have been identified, the hybrid
seed
to can be reproduced indefinitely as long as the homogeneity of the inbred
parents is
maintained.
Controlling Self-Pollination
Canola varieties are mainly self-pollinated; therefore, self-pollination of
the
parental varieties must be controlled to make hybrid development feasible. In
developing improved new Brassica hybrid varieties, breeders may use self-
incompatible (SI), cytoplasmic male sterile (CMS) or nuclear male sterile
(NMS)
Brassica plants as the female parent. In using these plants, breeders are
attempting to improve the efficiency of seed production and the quality of the
F1
hybrids and to reduce the breeding costs. When hybridization is conducted
without using SI, CMS or NMS plants, it is more difficult to obtain and
isolate the
desired traits in the progeny (F1 generation) because the parents are capable
of
undergoing both cross-pollination and self-pollination. If one of the parents
is a SI,
CMS or NMS plant that is incapable of producing pollen, only cross pollination
will
zi occur. By eliminating the pollen of one parental variety in a cross, a
plant breeder
is assured of obtaining hybrid seed of uniform quality, provided that the
parents
are of uniform quality and the breeder conducts a single cross.
In one instance, production of F1 hybrids includes crossing a CMS Brassica
female parent with a pollen-producing male Brassica parent. To reproduce
effectively, however, the male parent of the F1 hybrid must have a fertility
restorer
gene (Rf gene). The presence of an Rf gene means that the F1 generation will
not
be completely or partially sterile, so that either self-pollination or cross
pollination
may occur. Self-pollination of the F1 generation to produce several subsequent
13
generations is important to ensure that a desired trait is heritable and
stable and
that a new variety has been isolated.
An example of a Brassica plant which is cytoplasmic male sterile and used
for breeding is Ogura (OGU) cytoplasmic male sterile (Pellan-Delourme, et al.,
1987). A fertility restorer for Ogura cytoplasmic male sterile plants has been
transferred from Raphanus sativus (radish) to Brassica by lnstit. National de
Recherche Agricole (INRA) in Rennes, France (Pelletier, etal., 1987). The OGU
INRA restorer gene, Rf1 originating from radish, is described in WO 92/05251
and
in Delourme, et al., (1991). Improved versions of this restorer have been
developed. For example, see W098/27806, oilseed brassica containing an
improved fertility restorer gene for Ogura cytoplasmic male sterility.
Other sources and refinements of CMS sterility in canola include the Polima
cytoplasmic Male sterile plant, as well as those of US Patent Number
5,789,566,
DNA sequence imparting cytoplasmic male sterility, mitochondrial genome,
nuclear genome, mitochondria and plant containing said sequence and process
for the preparation of hybrids; US Patent Number 5,973,233 Cytoplasmic male
sterility system production canola hybrids; and W097/02737 Cytoplasmic male
sterility system producing canola hybrids; EP Patent Publication Number 0
599042A Methods for introducing a fertility restorer gene and for producing Fl
hybrids of Brassica plants thereby; US Patent Number 6,229,072 Cytoplasmic
male sterility system production canola hybrids; US Patent Number 4,658,085
Hybridization using cytoplasmic male sterility, cytoplasmic herbicide
tolerance, and
herbicide tolerance from nuclear genes.
Promising advanced breeding lines commonly are tested and compared to
appropriate standards in environments representative of the commercial target
area(s). The best lines are candidates for new commercial lines; and those
still
deficient in a few traits may be used as parents to produce new populations
for
further selection.
Inbred Development ¨ Female
The female parent of PV 200 CL was developed by crossing a male sterile
version of inbred NS6513 (A-line) with a maintainer line of inbred NS6513 (B-
line).
The A and B lines are genetically alike except the A-line carries the OGU INRA
cytoplasm, while the B-line carries the normal B. napus cytoplasm.
14
CA 2893598 2018-08-28
CA 02893598 2015-06-05
The B-line was developed using doubled haploidy method from a complex
cross. The last crossing was completed in 2004 and the DH lines were extracted
later in 2004. These were evaluated in the field nursery in 2005 and 2006 for
imidazolinone tolerance, early maturity, lodging resistance, high oil and
protein,
general vigor and uniformity. Backcrossing was carried out in the greenhouse
to
transfer the OGU INRA cytoplasm. Breeder Seed for the A line was bulked at
BC7.
Inbred Development ¨ Male
A male parent or restorer (R line) of variety NS7364 is designated
NS7364MI. The restorer was developed using pedigree method from a three way
cross where the last crossing was in 2005. The F2 bulk from the three-way
cross
was planted in Henley (SK) nursery for selfing. The F3s were then sent to
Chile
for further selfing and IMI screening. The F4 lines were evaluated in 2008 in
is Saskatoon for imidazolinone tolerance, general vigor, uniformity,
maturity, oil %,
protein %, total glucosinolates, total saturates, etc. Remnant seed of the
selected
F4 was then sent to Chile in 2008-2009 for F5 production. The individual F5s
were
evaluated and selfed in the 2009 nursery for similar traits as in 2008. The
selected
F6s were assigned new numbers and were testcrossed to a single tester. Based
on testcross performance a line was selected and was assigned a permanent
number. Pure inbred seed from the selected F6s was increased and then used to
produce hybrid seed. Using this restorer line, hybrid 12N11461 was produced
and
evaluated in two years of replicated yield trials. The hybrid 12N1146I was
evaluated in 2013 Private trials and 2014 Public trials.
Hybrid Development
PV 200 CL (12N11461) is a fully restored spring Brassica napus hybrid with
the Imidazolinone resistance, based on OGU INRA system developed in
Saskatoon. It is a single cross hybrid produced by crossing a female parent
(male
sterile inbred-A line x maintainer inbred-B line) carrying the imidazolinone
resistance genes by a restorer ¨ male R line (also carrying the imidazolinone
resistance genes), where A and B lines are genetically alike except the A line
carries the OGU INRA cytoplasm, while the B line carries the normal B. napus
cytoplasm.
CA 02893598 2015-06-05
A pollination control system and effective transfer of pollen from one parent
to the other offers improved plant breeding and an effective method for
producing
hybrid canola seed and plants. For example, the Ogura cytoplasmic male
sterility
(CMS) system, developed via protoplast fusion between radish (Raphanus
sativus) and rapeseed (Brassica napus), is one of the most frequently used
methods of hybrid production. It provides stable expression of the male
sterility
trait (Ogura, 1968, Pelletier, et al., 1983) and an effective nuclear restorer
gene
(Heyn, 1976).
For most traits the true genotypic value may be masked by other
to confounding plant traits or environmental factors. One method for
identifying a
superior plant is to observe its performance relative to other experimental
plants
and to one or more widely grown standard varieties. If a single observation is
inconclusive, replicated observations provide a better estimate of the genetic
worth.
Proper testing should detect any major faults and establish the level of
superiority or improvement over current varieties. In addition to showing
superior
performance, there must be a demand for a new variety that is compatible with
industry standards or which creates a new market. The introduction of a new
variety commonly will incur additional costs to the seed producer, the grower,
the
processor and the consumer, for special advertising and marketing, altered
seed
and commercial production practices, and new product utilization. The testing
preceding release of a new variety should take into consideration research and
development costs as well as technical superiority of the final variety. For
seed-
propagated varieties, it must be feasible to produce seed easily and
economically.
These processes, which lead to the final step of marketing and distribution,
usually take from approximately six to twelve years from the time the first
cross is
made. Therefore, the development of new varieties is a time-consuming process
that requires precise forward planning, efficient use of resources, and a
minimum
of changes in direction.
Further, as a result of the advances in sterility systems, lines are developed
that can be used as an open pollinated variety (i.e., a pureline cultivar sold
to the
grower for planting) and/or as a sterile inbred (female) used in the
production of F1
hybrid seed. In the latter case, favorable combining ability with a restorer
(male)
16
CA 02893598 2015-06-05
would be desirable. The resulting hybrid seed would then be sold to the grower
for planting.
Combining ability of a line, as well as the performance of the line per se, is
a factor in the selection of improved canola lines that may be used as
inbreds.
Combining ability refers to a line's contribution as a parent when crossed
with
other lines to form hybrids. The hybrids formed for the purpose of selecting
superior lines are designated test crosses. One way of measuring combining
ability is by using breeding values. Breeding values are based on the overall
mean of a number of test crosses. This mean is then adjusted to remove
to environmental effects and it is adjusted for known genetic relationships
among the
lines.
Hybrid seed production requires inactivation of pollen produced by the
female parent. Incomplete inactivation of the pollen provides the potential
for self-
pollination. This
inadvertently self-pollinated seed may be unintentionally
is harvested and packaged with hybrid seed. Similarly, because the male
parent is
grown next to the female parent in the field, there is also the potential that
the
male selfed seed could be unintentionally harvested and packaged with the
hybrid
seed. Once the seed from the hybrid bag is planted, it is possible to identify
and
select these self-pollinated plants. These self-pollinated plants will be
genetically
20 equivalent to one of the inbred lines used to produce the hybrid. Though
the
possibility of inbreds being included in hybrid seed bags exists, the
occurrence is
rare because much care is taken to avoid such inclusions. These self-
pollinated
plants can be identified and selected by one skilled in the art, through
either visual
or molecular methods.
25 Brassica
nopus Ganda plants, absent the use of sterility systems, are
recognized to commonly be self-fertile with approximately 70 to 90 percent of
the
seed normally forming as the result of self-pollination. The percentage of
cross
pollination may be further enhanced when populations of recognized insect
pollinators at a given growing site are greater. Thus open pollination is
often used
30 in commercial canola production.
Since canola variety PV 200 CL is a hybrid produced from substantially
homogeneous parents, it can be reproduced by planting seeds of such parents,
growing the resulting canola plants under controlled pollination conditions
with
17
CA 02893598 2015-06-05
adequate isolation so that cross-pollination occurs between the parents, and
harvesting the resulting hybrid seed using conventional agronomic practices.
Locus Conversions of Canola Variety PV 200 CL
PV 200 CL represents a new base genetic line into which a new locus or
trait may be introduced. Direct transformation and backcrossing represent two
important methods that can be used to accomplish such an introgression. The
term locus conversion is used to designate the product of such an
introgression.
To select and develop a superior hybrid, it is necessary to identify and
to .. select genetically unique individuals that occur in a segregating
population. The
segregating population is the result of a combination of crossover events plus
the
independent assortment of specific combinations of alleles at many gene loci
that
results in specific and unique genotypes. Once such a variety is developed its
value to society is substantial since it is important to advance the germplasm
base
is as a whole in order to maintain or improve traits such as yield, disease
resistance,
pest resistance and plant performance in extreme weather conditions. Locus
conversions are routinely used to add or modify one or a few traits of such a
line
and this further enhances its value and usefulness to society.
Backcrossing can be used to improve inbred varieties and a hybrid variety
20 which is made using those inbreds. Backcrossing can be used to transfer
a
specific desirable trait from one variety, the donor parent, to an inbred
called the
recurrent parent which has overall good agronomic characteristics yet that
lacks
the desirable trait. This transfer of the desirable trait into an inbred with
overall
good agronomic characteristics can be accomplished by first crossing a
recurrent
25 parent to a donor parent (non-recurrent parent). The progeny of this
cross is then
mated back to the recurrent parent followed by selection in the resultant
progeny
for the desired trait to be transferred from the non-recurrent parent.
Traits may be used by those of ordinary skill in the art to characterize
progeny. Traits are commonly evaluated at a significance level, such as a 1%,
5%
30 or 10% significance level, when measured in plants grown in the same
environmental conditions. For example, a locus conversion of PV 200 CL may be
characterized as having essentially the same phenotypic traits as PV 200 CL.
The
traits used for comparison may be those traits shown in any of Tables 1-6.
Molecular markers can also be used during the breeding process for the
selection
18
CA 02893598 2015-06-05
of qualitative traits. For example, markers can be used to select plants that
contain the alleles of interest during a backcrossing breeding program. The
markers can also be used to select for the genome of the recurrent parent and
against the genome of the donor parent. Using this procedure can minimize the
amount of genome from the donor parent that remains in the selected plants.
A locus conversion of PV 200 CL will retain the genetic integrity of PV 200
CL. A locus conversion of PV 200 CL will comprise at least 92%, 93%, 94%, 95%,
96%, 97%, 98% or 99% of the base genetics of PV 200 CL. For example, a locus
conversion of PV 200 CL can be developed when DNA sequences are introduced
to .. through backcrossing (Hallauer etal., 1988), with a parent of PV 200 CL
utilized
as the recurrent parent. Both naturally occurring and transgenic DNA sequences
may be introduced through backcrossing techniques. A backcross conversion
may produce a plant with a locus conversion in at least one or more
backcrosses,
including at least 2 crosses, at least 3 crosses, at least 4 crosses, at least
5
crosses and the like. Molecular marker assisted breeding or selection may be
utilized to reduce the number of backcrosses necessary to achieve the
backcross
conversion. For example, see Openshaw, S.J. etal., Marker-assisted Selection
in
Backcross Breeding. In: Proceedings Symposium of the Analysis of Molecular
Data, August 1994, Crop Science Society of America, Corvallis, OR, where it is
demonstrated that a backcross conversion can be made in as few as two
backcrosses.
Uses of Canola
Currently Brassica napus canola is being recognized as an increasingly
important oilseed crop and a source of meal in many parts of the world. The
oil as
removed from the seeds commonly contains a lesser concentration of
endogenously formed saturated fatty acids than other vegetable oils and is
well
suited for use in the production of salad oil or other food products or in
cooking or
frying applications. The oil also finds utility in industrial applications.
Additionally,
the meal component of the seeds can be used as a nutritious protein
concentrate
for livestock.
Canola oil has the lowest level of saturated fatty acids of all vegetable
oils.
"Canola" refers to rapeseed (Brassica) which (1) has an erucic acid (0221)
content
of at most 2 percent by weight based on the total fatty acid content of a
seed,
19
CA 02893598 2015-06-05
preferably at most 0.5 percent by weight and most preferably essentially 0
percent
by weight; and (2) produces, after crushing, an air-dried meal containing less
than
30 micromoles (p,mol) glucosinolates per gram of defatted (oil-free) meal.
These
types of rapeseed are distinguished by their edibility in comparison to more
traditional varieties of the species.
Disease - Sclerotinia
Sclerotinia infects over 100 species of plants, including numerous
economically important crops such as Brassica species, sunflowers, dry beans,
to soybeans, field peas, lentils, lettuce, and potatoes (Boland and Hall,
1994).
Sclerotinia sclerotiorum is responsible for over 99% of Sclerotinia disease,
while
Sclerotinia minor produces less than 1% of the disease. Sclerotinia produces
sclerotia, irregularly-shaped, dark overwintering bodies, which can endure in
soil
for four to five years. The
sclerotia can germinate carpogenically or
is myceliogenically, depending on the environmental conditions and crop
canopies.
The two types of germination cause two distinct types of diseases. Sclerotia
that
germinate carpogenically produce apothecia and ascospores that infect above-
ground tissues, resulting in stem blight, stalk rot, head rot, pod rot, white
mold and
blossom blight of plants. Sclerotia that germinate myceliogenically produce
20 mycelia that infect root tissues, causing crown rot, root rot and basal
stalk rot.
Sclerotinia causes Sclerotinia stem rot, also known as white mold, in
Brassica, including canola. Canola is a type of Brassica having a low level of
glucosinolates and erucic acid in the seed. The sclerotia germinate
carpogenically
in the summer, producing apothecia. The
apothecia release wind-borne
25 ascospores that travel up to one Kilometer. The disease is favoured by
moist soil
conditions (at least 10 days at or near field capacity) and temperatures of 15-
25 C,
prior to and during canola flowering. The spores cannot infect leaves and
stems
directly; they must first land on flowers, fallen petals, and pollen on the
stems and
leaves. Petal age affects the efficiency of infection, with older petals more
likely to
30 .. result in infection (Heran, at al., 1999). The fungal spores use the
flower parts as
a food source as they germinate and infect the plant.
The severity of Sclerotinia in Brassica is variable, and is dependent on the
time of infection and climatic conditions (Heran, et al., 1999). The disease
is
CA 02893598 2015-06-05
favored by cool temperatures and prolonged periods of precipitation.
Temperatures between 20 and 25 C and relative humidities of greater than 80%
are required for optimal plant infection (Heran, et al., 1999). Losses ranging
from
to 100% have been reported for individual fields (Manitoba Agriculture, Food
and
5 .. Rural Initiatives, 2004). On average, yield losses are estimated to be
0.4 to 0.5
times the Sclerotinia sclerotiorum Field Severity score, a rating based on
both
percentage infection and disease severity. More information is provided herein
at
Example 4. For example, if a field has 20% infection (20/100 plants infected),
then
the yield loss would be about 10% provided plants are dying prematurely due to
to the infection of the main stem (rating 5-SSFS=20`)/0). If the plants are
affected
much less (rating 1-SSFS=4%), yield loss is reduced accordingly. Further,
Sclerotinia can cause heavy losses in wet swaths. Sclerotinia sclerotiorum
caused economic losses to canola growers in Minnesota and North Dakota of
17.3, 20.8, and 16.8 million dollars in 1999, 2000 and 2001, respectively
(Bradley,
is et al. 2006). In Canada, this disease is extremely important in Southern
Manitoba,
parts of South Central Alberta and also in Eastern areas of Saskatchewan.
Since
weather plays an important role in development of this disease, its occurrence
is
irregular and unpredictable. Certain reports estimate about 0.8 to 1.3 million
acres
of canola being sprayed with fungicide in Southern Manitoba annually. The
20 fungicide application costs about $25 per acre, which represents a
significant cost
for canola producers. Moreover, producers may decide to apply fungicide based
on the weather forecast, while later changes in the weather pattern discourage
disease development, resulting in wasted product, time, and fuel. Creation of
Sclerotinia tolerant canola cultivars has been an important goal for many of
the
25 Canadian canola breeding organizations.
The symptoms of Sclerotinia infection usually develop several weeks after
flowering begins. The plants develop pale-grey to white lesions, at or above
the
soil line and on upper branches and pods. The infections often develop where
the
leaf and the stem join because the infected petals lodge there. Once plants
are
30 infected, the mold continues to grow into the stem and invade healthy
tissue.
Infected stems appear bleached and tend to shred. Hard black fungal sclerotia
develop within the infected stems, branches, or pods. Plants infected at
flowering
produce little or no seed. Plants with girdled stems wilt and ripen
prematurely.
Severely infected crops frequently lodge, shatter at swathing, and make
swathing
21
CA 02893598 2015-06-05
more time consuming. Infections can occur in all above-ground plant parts,
especially in dense or lodged stands, where plant-to-plant contact facilitates
the
spread of infection. New sclerotia carry the disease over to the next season.
Conventional methods for control of Sclerotinia diseases include (a)
.. chemical control, (b) disease resistance and (c) cultural control, each of
which is
described below.
(a) Fungicides such as benomyl, vinclozolin and iprodione remain the
main method of control of Sclerotinia disease (MoraII, et al., 1985; Tu,
1983).
Recently, additional fungicidal formulations have been developed for use
against
.. Sclerotinia, including azoxystrobin, prothioconazole, and boscalid.
(Johnson,
2005) However, use of fungicide is expensive and can be harmful to the user
and
environment. Further, resistance to some fungicides has occurred due to
repeated use.
(b) In certain cultivars of bean, safflower, sunflower and soybean, some
is .. progress has been made in developing partial (incomplete) resistance.
Partial
resistance is often referred to as tolerance. However, success in developing
partial resistance has been very limited, probably because partial
physiological
resistance is a multigene trait as demonstrated in bean (Fuller, et al.,
1984). In
addition to partial physiological resistance, some progress has been made to
.. breed for morphological traits to avoid Sclerotinia infection, such as
upright growth
habit, lodging resistance and narrow canopy. For example, bean plants with
partial physiological resistance and with an upright stature, narrow canopy
and
indeterminate growth habit were best able to avoid Sclerotinia (Saindon, et
al.,
1993). Early maturing cultivars of safflower showed good field resistance to
.. Sclerotinia. Finally, in soybean, cultivar characteristics such as height,
early
maturity and great lodging resistance result in less disease, primarily
because of a
reduction of favorable microclimate conditions for the disease. (Boland and
Hall,
1987; Buzzell, etal. 1993)
(c) Cultural practices, such as using pathogen-free or fungicide-treated
seed, increasing row spacing, decreasing seeding rate to reduce secondary
spread of the disease, and burying sclerotia to prevent carpogenic
germination,
may reduce Sclerotinia disease but not effectively control the disease.
Canola genotypes can be susceptible to Sclerotinia stem rot. This includes
all known spring petalled genotypes of canola quality. There is also no
resistance
22
CA 02893598 2015-06-05
to Sclerotinia in Australian canola varieties. (Hind-Lanoiselet, et al. 2004).
Some
varieties with certain morphological traits are better able to withstand
Sclerotinia
infection. For example, Polish varieties (Brassica rapa) have lighter canopies
and
seem to have much lower infection levels. In addition, petal-less varieties
(apetalous varieties) avoid Sclerotinia infection to a greater extent
(Okuyama, et
al., 1995; Fu, 1990). Other examples of morphological traits which confer a
degree of reduced field susceptibility in Brassica genotypes include increased
standability, reduced petal retention, branching (less compact and/or higher),
and
early leaf abscission. Jurke and Fernando, (2003) screened eleven canola
o genotypes for Sclerotinia disease incidence. Significant variation in
disease
incidence was explained by plant morphology, and the difference in petal
retention
was identified as the most important factor. However, these morphological
traits
alone do not confer resistance to Sclerotinia, and all canola products in
Canada
are considered susceptible to Sclerotinia.
Winter canola genotypes are also susceptible to Sclerotinia. In Germany,
for example, no Sc/erotinia-resistant varieties are available. (Specht, 2005)
The
widely-grown German variety Express is considered susceptible to moderately
susceptible and belongs to the group of less susceptible varieties/hybrids.
Spraying with fungicide is the only means of controlling Sclerotinia in canola
crops grown under disease-favorable conditions at flowering. Typical
fungicides
used for controlling Sclerotinia on Brassica include RovralTm/Proline TM from
Bayer
and RonilanTm/Lancen" from BASF. The active ingredient in LanceTM is Boscalid,
and it is marketed as EnduraTM in the United States. The fungicide should be
applied before symptoms of stem rot are visible and usually at the 20-30%
bloom
stage of the crop. If infection is already evident, there is no use in
applying
fungicide as it is too late to have an effect. Accordingly, growers must
assess their
fields for disease risk to decide whether to apply a fungicide. This can be
done by
using a government provided checklist or by using a petal testing kit. Either
method is cumbersome and prone to errors. (Hind-Lanoiselet, 2004; Johnson,
2005).
Numerous efforts have been made to develop Sclerotinia resistant Brassica
plants. Built-
in resistance would be more convenient, economical, and
environmentally-friendly than controlling Sclerotinia by application of
fungicides.
Since the trait is polygenic it would be stable and not prone to loss of
efficacy, as
23
1
CA 02893598 2015-06-05
fungicides may be. In some embodiments, PV 200 CL can be modified to have
resistance to Sclerotinia.
Characteristics of PV 200 CL
Homogenous and reproducible canola hybrids are useful for the production
of a commercial crop on a reliable basis. There are a number of analytical
methods available to determine the phenotypic stability of a canola hybrid.
The oldest and most traditional method of analysis is the observation of
phenotypic traits. The data are usually collected in field experiments over
the life
io of the
canola plants to be examined. Phenotypic characteristics most often are
observed for traits associated with seed yield, seed oil content, seed protein
content, fatty acid composition of oil, glucosinolate content of meal, growth
habit,
lodging resistance, plant height, shatter resistance, etc.
In addition to phenotypic observations, the genotype of a plant can also be
examined. A plant's genotype can be used to identify plants of the same
variety or
a related variety. For example, the genotype can be used to determine the
pedigree of a plant. There are many laboratory-based techniques available for
the
analysis, comparison and characterization of plant genotype; among these are
lsozyme Electrophoresis, Restriction Fragment Length Polymorphisms (RFLPs),
Randomly Amplified Polymorphic DNAs (RAPDs), Arbitrarily Primed Polymerase
Chain Reaction (AP-PCR), DNA Amplification Fingerprinting (DAF), Sequence
Characterized Amplified Regions (SCARs), Amplified Fragment Length
Polymorphisms (AFLPs), Simple Sequence Repeats (SSRs) which are also
referred to as Microsatellites, and Single Nucleotide Polymorphisms (SNPs).
The variety of the present invention has shown uniformity and stability for
all traits, as described in the following variety description information. The
variety
has been increased with continued observation for uniformity.
PV 200 CL is a medium maturing, high yielding lmidazolinone tolerant
Brassica napus canola hybrid having resistant (R) rating for blackleg and
resistant
(R) rating for Fusarium wilt. Its oil content is similar to the WCC/RRC
checks. Its
protein and chlorophyll contents are higher than the checks.
Table 1 provides data on morphological, agronomic, and quality traits for
PV 200 CL and canola variety 46H75. When preparing the detailed phenotypic
information that follows, plants of the new PV 200 CL variety were observed
while
24
CA 02893598 2015-06-05
being grown using conventional agronomic practices. For comparative purposes,
canola plants of canola varieties, 46H75 was similarly grown in a replicated
experiment.
Observations were recorded on various morphological traits for the hybrid
PV 200 CL and comparative check cultivars. (See Table 1).
Hybrid PV 200 CL can be advantageously used in accordance with the
breeding methods described herein and those known in the art to produce
hybrids
and other progeny plants retaining desired trait combinations of PV 200 CL.
This
invention is thus also directed to methods for producing a canola plant by
crossing
113 a first parent canola plant with a second parent canola plant wherein
either the first
or second parent canola plant is canola variety PV 200 CL. Further, both first
and
second parent canola plants can come from the canola variety PV 200 CL. Either
the first or the second parent plant may be male sterile.
Still further, this invention also is directed to methods for producing a PV
is 200 CL-derived canola plant by crossing canola variety PV 200 CL with a
second
canola plant and growing the progeny seed, and repeating the crossing and
growing steps with the canola PV 200 CL-derived plant from 1 to 2 times, 1 to
3
times, 1 to 4 times, or 1 to 5 times. Thus, any such methods using the canola
variety PV 200 CL are part of this invention: open pollination, selfing,
backcrosses,
20 hybrid production, crosses to populations, and the like. All plants
produced using
canola variety PV 200 CL as a parent are within the scope of this invention,
including plants derived from canola variety PV 200 CL. This includes canola
lines
derived from PV 200 CL which include components for either male sterility or
for
restoration of fertility. Advantageously, the canola variety is used in
crosses with
25 other, different, canola plants to produce first generation (F1) canola
hybrid seeds
and plants with superior characteristics.
The invention also includes a single-gene conversion of PV 200 CL. A
single-gene conversion occurs when DNA sequences are introduced through
traditional (non-transformation) breeding techniques, such as backcrossing.
DNA
30 sequences, whether naturally occurring or transgenes, may be introduced
using
these traditional breeding techniques. Desired traits transferred through this
process include, but are not limited to, fertility restoration, fatty acid
profile
modification, other nutritional enhancements, industrial enhancements, disease
resistance, insect resistance, herbicide resistance and yield enhancements.
The
CA 02893598 2015-06-05
trait of interest is transferred from the donor parent to the recurrent
parent, in this
case, the canola plant disclosed herein. Single-gene traits may result from
the
transfer of either a dominant allele or a recessive allele. Selection of
progeny
containing the trait of interest is done by direct selection for a trait
associated with
a dominant allele. Selection of progeny for a trait that is transferred via a
recessive allele will require growing and selfing the first backcross to
determine
which plants carry the recessive alleles. Recessive traits may require
additional
progeny testing in successive backcross generations to determine the presence
of
the gene of interest.
It should be understood that the canola variety of the invention can, through
routine manipulation by cytoplasmic genes, nuclear genes, or other factors, be
produced in a male-sterile or restorer form as described in the references
discussed earlier. Such embodiments are also within the scope of the present
claims. Canola variety PV 200 CL can be manipulated to be male sterile by any
of
is a number of methods known in the art, including by the use of mechanical
methods, chemical methods, self-incompatibility (SI), cytoplasmic male
sterility
(CMS) (either Ogura or another system), or nuclear male sterility (NMS). The
term
"manipulated to be male sterile" refers to the use of any available techniques
to
produce a male sterile version of canola variety PV 200 CL. The male sterility
may be either partial or complete male sterility. This invention is also
directed to
Fl hybrid seed and plants produced by the use of Canola variety PV 200 CL.
Canola variety PV 200 CL can also further comprise a component for fertility
restoration of a male sterile plant, such as an Rf restorer gene. In this
case,
canola variety PV 200 CL could then be used as the male plant in hybrid seed
production.
This invention is also directed to the use of PV 200 CL in tissue culture. As
used herein, the term plant includes plant protoplasts, plant cell tissue
cultures
from which canola plants can be regenerated, plant calli, plant clumps, and
plant
cells that are intact in plants or parts of plants, such as embryos, pollen,
ovules,
seeds, flowers, kernels, ears, cobs, leaves, husks, stalks, roots, root tips,
anthers,
silk and the like. PauIs, et al., (2006) (Canadian J of Botany 84(4):668-678)
confirmed that tissue culture as well as microspore culture for regeneration
of
canola plants can be accomplished successfully. Chuong, etal., (1985) "A
Simple
Culture Method for Brass/ca Hypocotyl Protoplasts", Plant Cell Reports 4:4-6;
26
CA 02893598 2015-06-05
Barsby, et al., (Spring 1996) "A Rapid and Efficient Alternative Procedure for
the
Regeneration of Plants from Hypocotyl Protoplasts of Brassica napus", Plant
Cell
Reports; Kartha, et al., (1974) "In vitro Plant Formation from Stem Explants
of
Rape", PhysioL Plant 31:217-220; Narasimhulu, et al., (Spring 1988) "Species
Specific Shoot Regeneration Response of Cotyledonary Explants of Brassicas",
Plant Cell Reports; Swanson, (1990) "Microspore Culture in Brassica", Methods
in
Molecular Biology 6(17):159; "Cell Culture techniques and Canola improvement"
J.
Am. Oil Chem. Soc. 66(4):455-56 (1989). Thus, it is clear from the literature
that
the state of the art is such that these methods of obtaining plants are, and
were,
io "conventional" in the sense that they are routinely used and have a very
high rate
of success.
The utility of canola variety PV 200 CL also extends to crosses with other
species. Commonly, suitable species will be of the family Brassicae.
The advent of new molecular biological techniques has allowed the
is isolation and characterization of genetic elements with specific
functions, such as
encoding specific protein products.
Scientists in the field of plant biology
developed a strong interest in engineering the genome of plants to contain and
express foreign genetic elements, or additional, or modified versions of
native or
endogenous genetic elements in order to alter the traits of a plant in a
specific
20 manner. Any DNA sequences, whether from a different species, or from the
same
species that are inserted into the genome using transformation are referred to
herein collectively as "transgenes". Over the last fifteen to twenty years
several
methods for producing transgenic plants have been developed, and the present
invention, in particular embodiments, also relates to transformed versions of
the
25 claimed canola variety PV 200 CL.
Numerous methods for plant transformation have been developed,
including biological and physical plant transformation protocols. See, for
example,
Miki, et al., "Procedures for Introducing Foreign DNA into Plants" in Methods
in
Plant Molecular Biology and Biotechnology, Glick, and Genetic Transformation
for
30 the improvement of Canola World Conf, Biotechnol. Fats and Oils Ind. 43-46
(1988). In addition, expression vectors and in vitro culture methods for plant
cell
or tissue transformation and regeneration of plants are available. See, for
example, Gruber, et al., "Vectors for Plant Transformation" in Methods in
Plant
27
CA 02893598 2015-06-05
Molecular Biology and Biotechnology, Glick and Thompson, Eds. (CRC Press,
Inc., Boca Raton, 1993) pages 89-119.
The most prevalent types of plant transformation involve the construction of
an expression vector. Such a vector comprises a DNA sequence that contains a
gene under the control of or operatively linked to a regulatory element, for
example a promoter. The vector may contain one or more genes and one or more
regulatory elements.
A genetic trait which has been engineered into a particular canola plant
using transformation techniques could be moved into another line using
traditional
breeding techniques that are well known in the plant breeding arts. For
example,
a backcrossing approach could be used to move a transgene from a transformed
canola plant to an elite inbred line and the resulting progeny would comprise
a
transgene. Also, if an inbred line was used for the transformation then the
transgenic plants could be crossed to a different line in order to produce a
transgenic hybrid canola plant. As used herein, "crossing" can refer to a
simple X
by Y cross, or the process of backcrossing, depending on the context. Various
genetic elements can be introduced into the plant genome using transformation.
These elements include but are not limited to genes; coding sequences;
inducible,
constitutive, and tissue specific promoters; enhancing sequences; and signal
and
.. targeting sequences. See, US Patent Number 6,222,101.
With transgenic plants according to the present invention, a foreign protein
can be produced in commercial quantities. Thus, techniques for the selection
and
propagation of transformed plants, which are well understood in the art, yield
a
plurality of transgenic plants which are harvested in a conventional manner,
and a
foreign protein then can be extracted from a tissue of interest or from total
biomass. Protein extraction from plant biomass can be accomplished by known
methods which are discussed, for example, by Heney and Orr, (1981) Anal.
Biochem. 114:92-96.
A genetic map can be generated, primarily via conventional Restriction
Fragment Length Polymorphisms (RFLP), Polymerase Chain Reaction (PCR)
analysis, Simple Sequence Repeats (SSR), and Single Nucleotide Polymorphisms
(SNPs), which identifies the approximate chromosomal location of the
integrated
DNA molecule coding for the foreign protein. For exemplary methodologies in
this
regard, see, Glick and Thompson, METHODS IN PLANT MOLECULAR BIOLOGY
28
CA 02893598 2015-06-05
AND BIOTECHNOLOGY 269-284 (CRC Press, Boca Raton, 1993). Map
information concerning chromosomal location is useful for proprietary
protection of
a subject transgenic plant. If unauthorized propagation is undertaken and
crosses
made with other germplasm, the map of the integration region can be compared
to
similar maps for suspect plants, to determine if the latter have a common
parentage with the subject plant. Map comparisons would involve
hybridizations,
RFLP, PCR, SSR, SNP, and sequencing, all of which are conventional
techniques.
Likewise, by means of the present invention, plants can be genetically
io engineered to express various phenotypes of agronomic interest. Exemplary
transgenes implicated in this regard include, but are not limited to, those
categorized below.
1. Genes that confer resistance to pests or disease and that encode:
(A) Plant disease resistance genes. Plant defenses are often activated
is by specific interaction between the product of a disease resistance gene
(R) in the
plant and the product of a corresponding avirulence (Avr) gene in the
pathogen. A
plant variety can be transformed with cloned resistance gene to engineer
plants
that are resistant to specific pathogen strains. See, for example Jones, et
al.,
(1994) Science 266:789 (cloning of the tomato Cf-9 gene for resistance to
20 Cladosporium fulvum); Martin, et al., (1993) Science 262:1432 (tomato
Pto gene
for resistance to Pseudomonas syringae pv. tomato encodes a protein kinase);
Mindrinos, et al., (1994) Cell 78:1089 (Arabidopsis RSP2 gene for resistance
to
Pseudomonas syringae); McDowell and Woffenden, (2003) Trends Biotechnol.
21(4):178-83 and Toyoda, et al., (2002) Transgenic Res. 11(6):567-82. A plant
25 resistant to a disease is one that is more resistant to a pathogen as
compared to
the wild type plant.
(B) A gene conferring resistance to fungal pathogens, such as oxalate
oxidase or oxalate decarboxylase (Zhou, etal., (1998) P1. Physiol. 117(1):33-
41).
(C) A Bacillus thuringiensis (Bt) protein, a derivative thereof or a
30 synthetic polypeptide modeled thereon. See, for example, Geiser, et al.,
(1986)
Gene 48:109, who disclose the cloning and nucleotide sequence of a Bt delta-
endotoxin gene. Moreover, DNA molecules encoding delta-endotoxin genes can
be purchased from American Type Culture Collection (Manassas, VA), for
example, under ATCC Accession Numbers. 40098, 67136, 31995 and 31998.
29
Other examples of Bacillus thuringiensis transgenes being genetically
engineered
are given in the following patents and patent applications: 5,188,960;
5,689,052;
5,880,275; WO 91/114778; WO 99/31248; WO 01/12731; WO 99/24581; WO
97/40162 and US Patent Numbers 7,605,304 and 7,696,412 and US Publication
Number US2004/0091505.
(D) An insect-specific hormone or pheromone such as an ecdysteroid
and juvenile hormone, a variant thereof, a mimetic based thereon, or an
antagonist or agonist thereof. See, for example, the disclosure by Hammock, at
al., (1990) Nature 344:458, of baculovirus expression of cloned juvenile
hormone
to esterase, an inactivator of juvenile hormone.
(E) An insect-specific peptide which, upon expression, disrupts the
physiology of the affected pest. For example, see the disclosures of Regan,
(1994) J. Biol. Chem. 269:9 (expression cloning yields DNA coding for insect
diuretic hormone receptor) and Pratt, at al., (1989) Biochem. Biophys. Res.
Comm. 163:1243 (an allostatin is identified in Diploptera puntata);
Chattopadhyay,
et aL, (2004) Critical Reviews in Microbiology 30(1):33-54 2004; Zjawiony,
(2004)
J Nat Prod 67(2):300-310; Carlini and Grossi-de-Sa, (2002) Toxicon 40(11):1515-
1539; Ussuf, et aL, (2001) Curr 80(7):847-853
and Vasconcelos and Oliveira,
(2004) Toxicon 44(4):385-403. See also, US Patent Number 5,266,317 to
Tomalski, et al., who disclose genes encoding insect-specific, paralytic
neurotoxins.
(F) An enzyme responsible for a hyperaccumulation of a monterpene, a
sesquiterpene, a steroid, hydroxamic acid, a phenylpropanoid derivative or
another non-protein molecule with insecticidal activity.
(G) An enzyme involved in the modification, including the post-
translational modification, of a biologically active molecule; for example, a
glycolytic enzyme, a proteolytic enzyme, a lipolytic enzyme, a nuclease, a
cyclase,
a transaminase, an esterase, a hydrolase, a phosphatase, a kinase, a
phosphorylase, a polymerase, an elastase, a chitinase and a glucanase, whether
natural or synthetic. See PCT Application Number WO 93/02197 in the name of
Scott, et at., which discloses the nucleotide sequence of a callase gene. DNA
molecules which contain chitinase-encoding sequences can be obtained, for
example, from the ATCC under Accession Numbers 39637 and 67152. See also,
Kramer, at al., (1993) Insect Biochem. Molec. Biol. 23:691, who teach the
=
CA 2893598 2018-08-28
nucleotide sequence of a cDNA encoding tobacco hookworm chitinase, and
Kawalleck et al., (1993) Plant Molec. Biol. 21:673, who provide the nucleotide
sequence of the parsley ub14-2 polyubiquitin gene, US Patent Numbers
7,145,060,
7,087,810 and 6,563,020.
(H) A molecule that
stimulates signal transduction. For example, see the
disclosure by Botella, at al., (1994) Plant Molec. Blot 24:757, of nucleotide
sequences for mung bean calmodulin cDNA clones, and Griess, et al., (1994)
Plant Physiol. 104:1467, who provide the nucleotide sequence of a maize
calmodulin cDNA clone.
(I) A hydrophobic moment
peptide. See, PCT Application Number
W095/16776 and US Patent Number 5,580,852 (disclosure of peptide derivatives
of Tachyplesin which inhibit fungal plant pathogens) and PCT Application
Number
W095/18855 and US Patent Number 5,607,914 (teaches synthetic antimicrobial
peptides that confer disease resistance).
(J) A membrane permease, a
channel former or a channel blocker. For
example, see the disclosure by Jaynes, et al., (1993) Plant Sci. 89:43, of
heterologous expression of a cecropin-beta lytic peptide analog to render
transgenic tobacco plants resistant to Pseudomonas solanacearum.
(K) A viral-invasive protein or a complex toxin derived therefrom. For
example, the accumulation of viral coat proteins in transformed plant cells
imparts
resistance to viral infection and/or disease development effected by the virus
from
which the coat protein gene is derived, as well as by related viruses. See
Beachy,
at al., (1990) Ann. Rev. Phytopathol. 28:451. Coat protein-mediated resistance
has been conferred upon transformed plants against alfalfa mosaic virus,
cucumber mosaic virus, tobacco streak virus, potato virus X, potato virus Y,
tobacco etch virus, tobacco rattle virus and tobacco mosaic virus. Id.
(L) An insect-specific antibody or an immunotoxin derived therefrom.
Thus, an antibody targeted to a critical metabolic function in the insect gut
would
inactivate an affected enzyme, killing the insect. Cf. Taylor, et al.,
Abstract #497,
SEVENTH INT'L SYMPOSIUM ON MOLECULAR PLANT-MICROBE
INTERACTIONS (Edinburgh, Scotland, 1994) (enzymatic inactivation in transgenic
tobacco via production of single-chain antibody fragments).
31
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(M) A virus-specific antibody. See, for example, Tavladoraki, at al.,
(1993) Nature 366:469, who show that transgenic plants expressing recombinant
antibody genes are protected from virus attack.
(N) A developmental-arrestive protein produced in nature by a pathogen
or a parasite. Thus, fungal endo alpha-1,4-D-polygalacturonases facilitate
fungal
colonization and plant nutrient release by solubilizing plant cell wall homo-
alpha-
1,4-D-galacturonase. See, Lamb, at al., (1992) Bio/Technology 10:1436. The
cloning and characterization of a gene which encodes a bean
endopolygalacturonase-inhibiting protein is described by Toubart, et aL,
(1992)
lo Plant J. 2:367.
(0) A
developmental-arrestive protein produced in nature by a plant. For
example, Logemann, et aL, (1992) Bio/Technology 10:305, have shown that
transgenic plants expressing the barley ribosome-inactivating gene have an
increased resistance to fungal disease.
(P) Genes involved in the
Systemic Acquired Resistance (SAR)
Response and/or the pathogenesis related genes. Briggs, (1995) Current Biology
5(2):128-131, Pieterse and Van Loon, (2004) Curr. Opin. Plant Bio 7(4):456-64
and Somssich, (2003) Cell 113(7):815-6.
(0) Antifungal
genes (Cornelissen and Melchers, (1993) PL PhysioL
101:709-712 and Parijs, et aL, (1991) Planta 183:258-264 and Bushnell, at al.,
(1998) Can. J. of Plant Path. 20(2):137-149. Also see, US Patent Number
6,875,907.
(R) Detoxification genes, such as for fumonisin, beauvericin,
moniliformin and zearalenone and their structurally related derivatives. For
example, see, US Patent Number 5,792,931.
(S) Cystatin and cysteine proteinase inhibitors. See, US Patent Serial
Number 7,205,453.
(T) Defensin genes. See, W003/000863 and US Patent Serial Number
6,911,577.
(U) Genes that confer
resistance to Phytophthora Root Rot, such as the
Brassica equivalents of the Rps 1, Rps 1-a, Rps 1-b, Rps 1-c, Rps 1-d, Rps 1-
e,
Rps 1-k, Rps 2, Rps 3-a, Rps 3-b, Rps 3-c, Rps 4, Rps 5, Rps 6, Rps 7 and
other
Rps genes. See, for example, Shoemaker, at al, (1995) Phytophthora Root Rot
32
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Resistance Gene Mapping in Soybean, Plant Genome IV Conference, San Diego,
CA.
2. Genes that confer resistance to a herbicide, for example:
(A) A herbicide that
inhibits the growing point or meristem, such as an
imidazalinone or a sulfonylurea. Exemplary genes in this category code for
mutant ALS and AHAS enzyme as described, for example, by Lee, etal., (1988)
EMBO J. 7:1241, and Miki, et al., (1990) Theor. AppLGeneL 80:449,
respectively.
See also, US Patent Numbers 5,605,011; 5,013,659; 5,141,870; 5,767,361;
to 5,731,180; 5,304,732; 4,761,373; 5,331,107; 5,928,937 and 5,378,824; and
international publication WO 96/33270.
(B) Glyphosate (resistance imparted by mutant 5-enolpyruv1-3-
phosphikimate synthase (EPSP) and aroA genes, respectively) and other
phosphono compounds such as glufosinate (phosphinothricin acetyl transferase,
PAT) and Streptomyces hygroscopicus phosphinothricin-acetyl transferase, bar,
genes), and pyridinoxy or phenoxy propionic acids and cycloshexones (ACCase
inhibitor-encoding genes). See, for example, US Patent Number 4,940,835 to
Shah, et al., which discloses the nucleotide sequence of a form of EPSP which
can confer glyphosate resistance. See also, US Patent Number 7,405,074, and
related applications, which disclose compositions and means for providing
glyphosate resistance. US Patent Number 5,627,061 to Barry, et al., also
describes genes encoding EPSPS enzymes. See also, US Patent Numbers
6,566,587; 6,338,961; 6,248,876 131; 6,040,497; 5,804,425; 5,633,435;
5,145,783;
4,971,908; 5,312,910; 5,188,642; 4,940,835; 5,866,775; 6,225,114 Bl;
6,130,366;
5,310,667; 4,535,060; 4,769,061; 5,633,448; 5,510,471; Re. 36,449; RE 37,287
E;
and 5,491,288; and international publications EP1173580; WO 01/66704;
EP1173581 and EP1173582. A DNA molecule encoding a mutant aroA gene can
be obtained under ATCC Accession Number 39256, and the nucleotide sequence
of the mutant gene is disclosed in US Patent Number 4,769,061 to Comai.
European Patent Publication Number 0 333 033 to Kumada, etal., and US Patent
Number 4,975,374 to Goodman, et al., disclose nucleotide sequences of
glutamine synthetase genes which confer resistance to herbicides such as L-
phosphinothricin. The
nucleotide sequence of a phosphinothricin-acetyl-
transferase gene is provided in European Publication Number 0 242 246 to
33
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CA 02893598 2015-06-05
Leemans, et aL, De Greef, et al., (1989) Bioirechnology 7:61, describe the
production of transgenic plants that express chimeric bar genes coding for
phosphinothricin acetyl transferase activity. See also, US Patent Numbers
5,969,213; 5,489,520; 5,550,318; 5,874,265; 5,919,675; 5,561,236; 5,648,477;
5,646,024; 6,177,616 B1 and 5,879,903.
Exemplary of genes conferring
resistance to phenoxy propionic acids and cycloshexones, such as sethoxydim
and haloxyfop, are the Accl-S1, Accl-S2 and Accl-S3 genes described by
Marshall, etal., (1992) Theor. App!. Genet. 83:435. See also, US Patent
Numbers
5,188,642; 5,352,605; 5,530,196; 5,633,435; 5,717,084; 5,728,925; 5,804,425
and
Canadian Patent Number 1,313,830.
(C) A herbicide that inhibits photosynthesis, such as a triazine (psbA and
gs+ genes) and a benzonitrile (nitrilase gene). Przibilla, et al., (1991)
Plant Cell
3:169, describe the transformation of Chlamydomonas with plasmids encoding
mutant psbA genes. Nucleotide sequences for nitrilase genes are disclosed in
US
is Patent Number 4,810,648 to Stalker, and DNA molecules containing
these genes
are available under ATCC Accession Numbers 53435, 67441 and 67442. Cloning
and expression of DNA coding for a glutathione S-transferase is described by
Hayes, etal., (1992) Biochem. J. 285:173.
(D) Acetohydroxy acid synthase, which has been found to make plants
that express this enzyme resistant to multiple types of herbicides, has been
introduced into a variety of plants (see, e.g., Hattori, et aL, (1995) Mol Gen
Genet
246:419). Other genes that confer tolerance to herbicides include: a gene
encoding a chimeric protein of rat cytochrome P4507A1 and yeast NADPH-
cytochrome P450 oxidoreductase (Shiota, et al., (1994) Plant Physiol 106:17),
genes for glutathione reductase and superoxide dismutase (Aono, et al., (1995)
Plant Cell Physiol 36:1687, and genes for various phosphotransferases (Datta,
et
al., (1992) Plant Mol Biol 20:619).
(E) Protoporphyrinogen oxidase (protox) is necessary for the production
of chlorophyll, which is necessary for all plant survival. The protox enzyme
serves
as the target for a variety of herbicidal compounds. These herbicides also
inhibit
growth of all the different species of plants present, causing their total
destruction.
The development of plants containing altered protox activity which are
resistant to
these herbicides are described in US Patent Numbers 6,288,306 B1; 6,282,837
B1; and 5,767,373; and international publication WO 01/12825.
34
CA 02893598 2015-06-05
3. Transgenes that confer or contribute to an altered grain
characteristic, such
as:
(A) Altered fatty acids, for example, by
(1) Down-regulation of stearoyl-ACP desaturase to increase
stearic acid content of the plant. See, Knultzon, et al., (1992) Proc. Natl.
Acad. Sci. USA 89:2624 and W099/64579 (Genes for Desaturases to Alter
Lipid Profiles in Corn),
(2) Elevating oleic acid via FAD-2 gene modification and/or
decreasing linolenic acid via FAD-3 gene modification (see, US Patent
Numbers 6,063,947; 6,323,392; 6,372,965 and W093111245),
(3) Altering conjugated linolenic or linoleic acid content, such as
in WO 01/12800,
(4) Altering LEC1, AGP, Dek1, Superalt mi1ps, various Ipa
genes such as 'pat Ipa3, hpt or hggt. For example, see WO 02/42424,
WO 98/22604, WO 03/011015, US Patent Numbers 6,423,886, 6,197,561,
6,825,397, US Patent Application Publication Numbers 2003/0079247,
2003/0204870, W002/057439, W003/011015 and Rivera-Madrid, et al.,
(1995) Proc. Natl. Acad. Sci. 92:5620-5624.
(B) Altered phosphate content, for example, by the
(1) Introduction of a phytase-encoding gene would enhance
breakdown of phytate, adding more free phosphate to the transformed
plant. For example, see, Van Hartingsveldt, et al., (1993) Gene 127:87, for
a disclosure of the nucleotide sequence of an Aspergillus niger phytase
gene.
(2) Up-regulation of a gene that reduces phytate content. In
maize, this, for example, could be accomplished, by cloning and then re-
introducing DNA associated with one or more of the alleles, such as the
LPA alleles, identified in maize mutants characterized by low levels of
phytic acid, such as in Raboy, et al., (1990) Maydica 35:383 and/or by
altering inositol kinase activity as in WO 02/059324, US Patent Application
Publication Number 2003/0009011, WO 03/027243, US Patent Application
Publication Number 2003/0079247, WO 99/05298, US Patent Numbers
6,197,561, 6,291,224, 6,391,348, W02002/059324, US Patent Application
CA 02893598 2015-06-05
Publication Number 2003/0079247, W098/45448, W099/55882,
W001/04147.
(C)
Altered carbohydrates effected, for example, by altering a gene for
an enzyme that affects the branching pattern of starch, a gene altering
thioredoxin.
(See, US Patent Number 6,531,648). See, Shiroza, et al., (1988) J. Bacteriol
170:810 (nucleotide sequence of Streptococcus mutans fructosyltransferase
gene), Steinmetz, et aL, (1985) MoL Gen. Genet. 200:220 (nucleotide sequence
of
Bacillus subtilis levansucrase gene), Pen, et al., (1992) Bio/Technology
10:292
(production of transgenic plants that express Bacillus licheniformis alpha-
amylase), Elliot, et al., (1993) Plant Molec Biol 21:515 (nucleotide sequences
of
tomato invertase genes), Sogaard, et al., (1993) J. Biol. Chem. 268:22480
(site-
directed mutagenesis of barley alpha-amylase gene) and Fisher, et al., (1993)
Plant Physiol 102:1045 (maize endosperm starch branching enzyme II), WO
99/10498 (improved digestibility and/or starch extraction through modification
of
UDP-D-xylose 4-epimerase, Fragile 1 and 2, Ref1, HCHL, C4H), US Patent
Number 6,232,529 (method of producing high oil seed by modification of starch
levels (AGP)). The fatty acid modification genes mentioned above may also be
used to affect starch content and/or composition through the interrelationship
of
the starch and oil pathways.
(D) Altered
antioxidant content or composition, such as alteration of
tocopherol or tocotrienols. For example, see, US Patent Number 6,787,683, US
Patent Application Publication Number 2004/0034886 and WO 00/68393 involving
the manipulation of antioxidant levels through alteration of a phytl prenyl
transferase (ppt), WO 03/082899 through alteration of a homogentisate geranyl
geranyl transferase (hggt).
(E)
Altered essential seed amino acids. For example, see, US Patent
Number 6,127,600 (method of increasing accumulation of essential amino acids
in
seeds), US Patent Number 6,080,913 (binary methods of increasing accumulation
of essential amino acids in seeds), US Patent Number 5,990,389 (high lysine),
W099/40209 (alteration of amino acid compositions in seeds), W099/29882
(methods for altering amino acid content of proteins), US Patent Number
5,850,016 (alteration of amino acid compositions in seeds), W098/20133
(proteins
with enhanced levels of essential amino acids), US Patent Number 5,885,802
(high methionine), US Patent Number 5,885,801 (high threonine), US Patent
36
CA 02893598 2015-06-05
Number 6,664,445 (plant amino acid biosynthetic enzymes), US Patent Number
6,459,019 (increased lysine and threonine), US Patent Number 6,441,274 (plant
tryptophan synthase beta subunit), US Patent Number 6,346,403 (methionine
metabolic enzymes), US Patent Number 5,939,599 (high sulfur), US Patent
Number 5,912,414 (increased methionine), W098/56935 (plant amino acid
biosynthetic enzymes), W098/45458 (engineered seed protein having higher
percentage of essential amino acids), W098/42831 (increased lysine), US Patent
Number 5,633,436 (increasing sulfur amino acid content), US Patent Number
5,559,223 (synthetic storage proteins with defined structure containing
programmable levels of essential amino acids for improvement of the
nutritional
value of plants), W096/01905 (increased threonine), W095/15392 (increased
lysine), US Patent Application Publication Number 2003/0163838, US Patent
Application Publication Number 2003/0150014, US Patent Application Publication
Number 2004/0068767, US Patent Number 6,803,498, W001/79516, and
is W000/09706 (Ces A: cellulose synthase), US Patent Number 6,194,638
(hemicellulose), US Patent Number 6,399,859 and US Patent Application
Publication Number 2004/0025203 (UDPGdH), US Patent Number 6,194,638
(RGP).
4. Genes that control pollination, hybrid seed production, or male-
sterility:
There are several methods of conferring genetic male sterility available,
such as multiple mutant genes at separate locations within the genome that
confer
male sterility, as disclosed in US Patent Numbers 4,654,465 and 4,727,219 to
Brar, et al., and chromosomal translocations as described by Patterson in US
Patents Numbers 3,661,709 and 3,710,511. In addition to these methods,
Albertsen, et al., US Patent Number 5,432,068, describe a system of nuclear
male
sterility which includes: identifying a gene which is critical to male
fertility; silencing
this native gene which is critical to male fertility; removing the native
promoter from
the essential male fertility gene and replacing it with an inducible promoter;
inserting this genetically engineered gene back into the plant; and thus
creating a
plant that is male sterile because the inducible promoter is not "on"
resulting in the
male fertility gene not being transcribed. Fertility is restored by inducing,
or
turning "on", the promoter, which in turn allows the gene that confers male
fertility
to be transcribed.
37
CA 02893598 2015-06-05
(A) Introduction of a deacetylase gene under the control of a tapetum-
specific promoter and with the application of the chemical N-Ac-PPT (WO
01/29237).
(B) Introduction of various stamen-specific promoters (WO 92/13956,
WO 92/13957).
(C) Introduction of the barnase and the barstar gene (Paul, etal., (1992)
Plant Mol. Biol. 19:611-622).
For additional examples of nuclear male and female sterility systems and
genes, see also, US Patent Numbers 5,859,341; 6,297,426; 5,478,369; 5,824,524;
5,850,014 and 6,265,640.
Also see, US Patent Number 5,426,041 (invention relating to a method for
the preparation of a seed of a plant comprising crossing a male sterile plant
and a
second plant which is male fertile), US Patent Number 6,013,859 (molecular
methods of hybrid seed production) and US Patent Number 6,037,523 (use of
is male tissue-preferred regulatory region in mediating fertility).
5. Genes that create a site for site specific DNA integration.
This includes the introduction of FRT sites that may be used in the
FLP/FRT system and/or Lox sites that may be used in the Cre/Loxp system. For
example, see, Lyznik, et al., (2003) "Site-Specific Recombination for Genetic
Engineering in Plants", Plant Cell Rep 21:925-932 and WO 99/25821. Other
systems that may be used include the Gin recombinase of phage Mu (Maeser, et
al., 1991), the Pin recombinase of E. coli (Enomoto, et al., 1983), and the
R/RS
system of the pSR1 plasmid (Araki, etal., 1992).
6. Genes that affect abiotic stress resistance (including but not limited
to
flowering, ear and seed development, enhancement of nitrogen utilization
efficiency, altered nitrogen responsiveness, drought resistance or tolerance,
cold
resistance or tolerance, and salt resistance or tolerance) and increased yield
under stress.
For example, see, WO 00/73475 where water use efficiency is altered
through alteration of malate; US Patent Numbers 5,892,009, 5,965,705,
5,929,305, 5,891,859, 6,417,428, 6,664,446, 6,706,866, 6,717,034, 6,801,104,
W02000060089, W02001026459, W02001035725, W02001034726,
38
W02001035727, W02001036444, W02001036597, W02001036598,
W02002015675, W02002017430, W02002077185, W02002079403,
W02003013227, W02003013228, W02003014327, W02004031349,
W02004076638, W09809521 and W09938977 describing genes, including CBF
s genes and transcription factors effective in mitigating the negative
effects of
freezing, high salinity, and drought on plants, as well as conferring other
positive
effects on plant phenotype; US Patent Application Publication Number
2004/0148654 and W001/36596 where abscisic acid is altered in plants resulting
in improved plant phenotype such as increased yield and/or increased tolerance
to
abiotic stress; W02000/006341, W004/090143, US Patent Numbers 7,531,723
and 6,992,237 where cytokinin expression is modified resulting in plants with
increased stress tolerance, such as drought tolerance, and/or increased yield.
Also see W00202776, W003052063, JP2002281975, US Patent Number
6,084,153, W00164898, US Patent Number 6,177,275 and US Patent Number
6,107,547 (enhancement of nitrogen utilization and altered nitrogen
responsiveness). For ethylene alteration, see, US Patent Application
Publication
Numbers 2004/0128719, 2003/0166197 and W0200032761. For plant
transcription factors or transcriptional regulators of abiotic stress, see
e.g., US
Patent Application Publication Number 2004/0098764 or US Patent Application
Publication Number 2004/0078852.
Other genes and transcription factors that affect plant growth and
agronomic traits such as yield, flowering, plant growth and/or plant
structure, can
be introduced or introgressed into plants, see, e.g., W097/49811 (LHY),
W098/56918 (ESD4), W097/10339 and US6573430 (TFL), US6713663 (FT),
W096/14414 (CON), W096/38560, W001/21822 (VRN1), W000/44918 (VRN2),
W099/49064 (GI), W000/46358 (FRI), W097/29123, US Patent Numbers
6,794,560, 6,307,126 (GAI), W099/09174 (D8 and Rht), and W02004076638 and
W02004031349 (transcription factors).
Seed Cleaning
This invention is also directed to methods for producing cleaned canola
seed by cleaning seed of variety PV 200 CL. "Cleaning a seed" or "seed
cleaning"
refers to the removal of foreign material from the surface of the seed.
Foreign
material to be removed from the surface of the seed includes but is not
limited to
39
CA 2893598 2018-08-28
CA 02893598 2015-06-05
fungi, bacteria, insect material, including insect eggs, larvae, and parts
thereof,
and any other pests that exist on the surface of the seed. The terms "cleaning
a
seed" or "seed cleaning" also refer to the removal of any debris or low
quality,
infested, or infected seeds and seeds of different species that are foreign to
the
sample. This invention is also directed to produce subsequent generations of
seed from seed of variety PV 200 CL, harvesting the subsequent generation of
seed; and planting the subsequent generation of seed.
Seed Treatment
"Treating a seed" or "applying a treatment to a seed" refers to the
application of a composition to a seed as a coating or otherwise. The
composition
may be applied to the seed in a seed treatment at any time from harvesting of
the
seed to sowing of the seed. The composition may be applied using methods
including but not limited to mixing in a container, mechanical application,
tumbling,
spraying, misting, and immersion. Thus, the composition may be applied as a
slurry, a mist, or a soak. The composition to be used as a seed treatment can
be
a pesticide, fungicide, insecticide, or antimicrobial. For a general
discussion of
techniques used to apply fungicides to seeds, see "Seed Treatment," 2d ed.,
(1986), edited by K. A Jeffs (chapter 9).
Industrial Applicability
The seed of the PV 200 CL variety, the plant produced from such seed,
various parts of the PV 200 CL hybrid canola plant or its progeny, a canola
plant
produced from the crossing of the PV 200 CL variety, and the resulting seed,
can
be utilized in the production of an edible vegetable oil or other food
products in
accordance with known techniques. The remaining solid meal component derived
from seeds can be used as a nutritious livestock feed.
CA 02893598 2015-07-17
DEPOSIT
Applicant(s) have made or will make a deposit of at least 2500 seeds of
canola variety PV 200 CL with the American Type Culture Collection (ATCC),
10801 University Boulevard, Manassas, VA 20110-2209 USA, ATCC Deposit No.
PTA-122193. The seeds deposited with the ATCC on May 29, 2015 for PTA-
122193 were taken from the seed stock maintained by Pioneer Hi-Bred
International, Inc., 7250 NW 62nd Avenue, Johnston, Iowa 50131-1000 since
prior
to the filing date of this application. Access to this deposit will be
available during
the pendency of the application to the Commissioner of Patents and Trademarks
lo and persons determined by the Commissioner to be entitled thereto upon
request.
Upon allowance of any claims in the application, the Applicant will make
available
to the public, pursuant to 37 C.F.R. 1.808, sample(s) of the deposit of at
least
2500 seeds of canola variety PV 200 CL with the American Type Culture
Collection (ATCC), 10801 University Boulevard, Manassas, VA 20110-2209. This
deposit of seed of canola variety PV 200 CL will be maintained in the ATCC
depository, which is a public depository, for a period of 30 years, or 5 years
after
the most recent request, or for the enforceable life of the patent, whichever
is
longer, and will be replaced if it becomes nonviable during that period.
Additionally, Applicant has satisfied all the requirements of 37 C.F.R.
1.801
.. 1.809, including providing an indication of the viability of the sample
upon deposit.
Applicant has no authority to waive any restrictions imposed by law on the
transfer
of biological material or its transportation in commerce. Applicant(s) do not
waive
any infringement of their rights granted under this patent or rights
applicable to
canola hybrid PV 200 CL under the Plant Variety Protection Act (7 USC 2321 et
seq.).
41
CA 02893598 2015-06-05
Varietal Characteristics (See also Tables 1 through 4)
Seed yield Approximately equal to the mean of the WCC/RRC checks.
Disease reaction Classified as Resistant (R) to blackleg (Leptospaera
maculans) according to
WCC/RRC guidelines. Classified as resistant (R) to Fusarium wilt according
to trials.
Plant height Approximately one-half cm shorter than the mean of the
WCC/RRC checks.
Maturity Nearly 1 day later maturing than the WCC/RRC checks.
Lodging Approximately equal to the mean of the WCC/RRC checks.
Herbicide tolerance Tolerant to imidazolinone herbicides. Field testing
confirms that PV 200 CL
tolerates the recommended rate of Solo WDG (Imazamox) (35 g ai/ha)
without showing plant injury or any significant negative effect on yield,
agronomic, and quality traits.
Variants Exhibits less than 1500/10,000 (<15%) sterile plants.
Seed Characteristics
Seed color Dark brown
Seed oil content Approximately equal to the mean of the WCC/RRC checks.
Seed protein content 0.7% lower than the mean of the WCC/RRC checks.
Erucic acid Less than 0.5% (maximum allowable limit).
Total saturates Approximately equal to the mean of the WCC/RRC checks.
Total glucosinolates Canola quality ¨ lower than the WCC/RRC checks.
Chlorophyll 1.5 ppm greater than the WCC/RRC checks.
42
CA 02893598 2015-06-05
Table 1. Variety Descriptions based on Morphological, Agronomic and Quality
Traits
PV 200 CL 46H76
(Check Variety)
Trait
Trait Rating Description Rating Description
Code
1.2 Seasonal Type Spring
Cotyledon width
3=narrow
2.1 5 Medium 6 Medium to Wide
5=medium
7=wide
Seedling growth
habit (leaf rosette)
2.2 5 5
1=weak rosette
9 = strong rosette
Stem anthocyanin
intensity
1=absent or very
weak 1 Absent or very 1 Absent or very
2*3 3=weak weak weak
5=medium
7=strong
9=very strong
Leaf type
2.4 1=petiolate 4 9
9=lyrate
Leaf shape
2.5 3=narrow elliptic 3 Narrow elliptic 3 Narrow elliptic
7=orbicular
Leaf length
3=short
Medium 5 Medium
2.6 5=medium
7=long
Leaf width
3=narrow
2.7 6 Medium to Wide 5 Medium
5=medium
7=wide
Leaf color
1=light green
2.8 2=medium green 2 Medium green 2 Medium green
3=dark green
4=b1ue-green
Leaf lobe
development
1=absent or very
4
weak Weak to 3 Weak
2'12 3=weak Medium
5=medium
7=strong
9=very strong
3 2.13
Number of leaf 2
lobes
Petiole length
3=short
2.15 5 Medium 5 Medium
5=medium
7=long
Leaf margin shape
1=undulating
2.16 3 Sharp 3 Sharp
2=rounded
3=sharp
43
CA 02893598 2015-06-05
PV 200 CL 46H75
(Check Variety)
Trait
Trait Rating Description Rating
Description
Code
Leaf margin
indentation
1=absent or very
weak (very shallow)
Weak (shallow) Weak (shallow) to
2.17 3=weak (shallow) 4 4
5=medium
to Medium Medium
7=strong (deep)
9=very strong (very
deep)
Leaf attachment to
stem
1=complete
2.18 clasping 2 Partial clasping 2 Partial clasping
2=partial clasping
3=non-clasping
3.1 Flower date 50% 47.5
Plant height at
maturity
3.2 3=short 7 Tall
5=medium
7=tall
Flower bud location
1=buds above most
recently opened Buds above Buds above most
3.4 flowers 1 most recently 1 recently opened
9=buds below most opened flowers flowers
recently opened
,flowers
Petal color
1=white
2=light yellow
3.5 3=medium yellow 3 Medium yellow 3 Medium yellow
4=dark yellow
5=orange
6=other
Petal length
3=short
3.6 5 Medium 5 Medium
5=medium
7=long
Petal width
3=narrow
3.7 5 Medium 5 Medium
5=medium
7=wide
Petal spacing
1=open
3=not touching
3.8 3 Not touching Not touching
5=touching
7=slight overlap
9=strong1y overlap
Anther fertility
1=sterile All anthers All anthers
3.11 9 9
g=all anthers shedding pollen shedding pollen
shedding pollen
Pod (silique) length
1=short (<7cm)
3.12 5=medium (7- 6 4
10cm)
9=1ong (>10cm)
Pod (silique) width
3=narrow (3mm) 6 Medium (4 mm) 6 Medium (4 mm) to
3.13
5=medium (4 mm) to Wide (5 mm) Wide (5 mm)
7=wide (5mm)
44
CA 02893598 2015-06-05
PV 200 CL 46H75
(Check Variety)
Trait
Trait Rating Description Rating Description
Code
Pod (silique)
attitude
1=erect
3.14 3=semi-erect 3 Semi-erect 3 Semi-erect
5=horizontal
7=slightly drooping
9=drooping
Pod (silique) beak
length
3.15 3=short 5 Medium 5 Medium
5=medium
7=long
Pedicel length
3=short
3.16 5 medium 5 medium
5=medium
7=long
Maturity (days 3.17 from97.3
planting)
Seed coat color
1=black
2=brown
4.1 3=tan 1.5 Black to brown 1.5 Black to brown
4=yellow
5=mixed
6=other
Lodging resistance
1=not tested
3=poor
5.2 7.2
5=fair
7=good
9=excellent
Blackleg resistance
0=not tested
i=resistant
3=moderately
resistant
6.3 1 Resistant
5=moderately
susceptible
7=susceptible
9=highly
susceptible
Fusarium wilt
resistance
0=not tested
1=resistant
3=moderately
6.7 resistant I Resistant
5=moderately
susceptible
7=susceptible
9=highly
susceptible
Oil content
8.1 (percentage, whole 48.6
dry seed basis)
Fatty acids
(expressed as a
percentage of total
fatty acids in seed
8.2.7 6.4
oil)
Total saturated fats
content
CA 02893598 2015-06-05
PV 200 CL 46H75
(Check Variety)
Trait
Trait Rating Description Rating Description
Code
Protein content
(percentage, whole
8.5 44.1
oil-free dry seed
basis)
Glucosinolates
Content (pmoles of
total glucosinolates
per gram whole
seed), 8.5%
moisture basis)
8.7
1= very low 2 Low (10-15
(<10pmol per gram) pmol per gram)
2= low (10-15 limo)
per gram)
3=medium (15-
20010I per gram)
4=hi9h (>20 pmol
per gram)
46
CA 02893598 2015-06-05
Example 1. Herbicide Resistance
Appropriate field tests have shown that PV 200 CL tolerates the recommended
rate
of Solo WDG (Imazamox) (35 g ai/ha) without showing plant injury or any
significant
negative effect on yield, agronomic, and quality traits.
Table 2. Effect of herbicide application on agronomic and quality traits of PV
200
CL in herbicide tolerance trials in 2013 and 2014
2013 Vegreville, AB 2VGH
i
c ?..
>,
>, a) -...-c ri: -.q. o..2 - o...,, 2 ! o ou t
A) E u li; -8 `'. ) -8 >), 2 u-0 -1- 2 6 I!,
82_ @) o.
2
itl III -0 -
a, >- -2 6 037s. 5 cot_ =-= : .cy) 2 ..': o_
4.
> co - o .c
I- 5_- " Z-- 15 ' o. =J5 1' a_ 0
- 0 co - ,- ca Zs' ! 1) >, 6 ' c)
a),- a) CNI CO
I I
PV 200 CL 2X 25.8 101.3 3 0 52.7 110.0
104.49.5 43.7 93.2 12 5
7
. ,
PV 200 CL WF 25.4 0 0 52.0 108.3 104.49.7
42.6 92.3 12 8
7
12.6
CV% 47 1.2
5.3 1.6 2.20 3.10 0.90 10.6 38.1
0
LSD (0.05) 5.37 2 1.3 9.7 3.4 1.80 2.40
1.40 2.1 5.9
,
SE 1.90 0.78 0.42 1 3.47 1.20 0.64 0.85 0.50
0.71 2.05
1
1
2013 Saskatoon, SK 2SSH
, .= (/) c
- *E- a .0 E E. 9 0 E ..'--->,
>, o g - IT..,
.a) ? -t- li 1". a) en ra a) u) ici u- ..., .4 0 0
6.- a o.
7 ct..S-..) 7 (>,:-,, 2 o .o 2
> E.) a) >- Z-i,,,' .9 -0 a .C2 -0 "c3. . !a) 2 c'-;
0- + . 12
1- -2 0, ,9- -.9 - 2- ,,,., 1) e) .., 6, g
0
i' - " - 0 6 CD
PV 200 CL 2X 26.6 110.8 0 0 49.0
105.0 95.0 47.2 44.2 91.3 11 6
PV 200 CL WE 24.0 0 0 48.0 108.0 97.0 48.0
43.2 91.3 11 4
CV% 13.8 267
267.2 3.5 8.1 1.8 2.40 2.40 0.90 10.6 61.5
LSD (0.05) 54 1 1.0 3.0 14.0 3.0 1.90 1.80
1.30 1.8 6.2
SE 1.91 0.00 0.00 0.71
4.95 0.71 0.64 064 0.50 0.64 2.19
47
CA 02 8935 98 2015-06-05
2013 Rosebank, MB 3RBY
a' 17; = r)
,=''-'
. . . 3
E 0 0 E 0 o 0 "f S =
>,
, E -0 E.L."---. - L.- -.., - a- ..,.., 7 ..L-', r. -
i3 s
.a) a- ,..,, z a) th CI I a) o M - 5
'63- it; 10 . µi= -- D>.,3 . (2 72 c ,3- . 2 0 _=
2
0) P-= a- + ,.0) iD
> 2 a) >" '`Z .9_ -0 a .9 -0 li. u,
I-- - Ã o 2- -2 - - 1 0)
>, .. - 0
0 - 0 c7i (6 (77 0 5 =7 -0
I I 0 c lj
PV 200 CL 2X 31.0 93.1 1 0 43.0 127.0 96.0 48.1
44.7 92.8 13 1
PV 200 CL WE 33.3 0 0 43.0 138.0 94.0
47.3 46.0 93.3 15 3
CV% 12.0 34 1.4 5.0 1.5 2.0 2.4 0.6
6.9 21.5
LSD (0.05) 6.1 1 1.0 12.0 2.0 2.1 2.50 1.20
2.2 1.6
SE 2.12 0.00 0.7 4.24 0.71
0.7 0.85 0.42 0.78 0.57
2013 Treherne, MB 3TRY
c =',z
-6'
a.. E 2,_ .o o0 -- g C
' ="
,. tz' '2:.T.2 a) u) aa a) co M I-1- ,---
'-' -6
(,, .52 79. g= =!--) 0 _c 2
2 a) >- ..' .i--2 .0 -51 .9_ -0 -"Ei . c).) .53 -<=,'
CL + 0) 0
I- -2 cp a -2 a (1. 1),- 0
> , ?A' o= o-m 8-
C6
I I 0 C
PV 200 CL 2X 26.0 91.5 0 0 41.0 127.0
99.0 48.2 45.8 94.0 13 3
PV 200 CL WF 28.4 0 0 41.0 127.0 97.0
47.4 47.6 95.0 15 3
CV% 10.1 30 183.7 1.3
6.1 1.7 2.00 3.10 1.10 6.2 76.4
LSD (0.05) 4.4 0 1.0 1.0 13.0 3.0 2.00 3.00
2.20 1.9 3.9
SE 1.56 0.00 0.71 0.00
4.95 0.71 0.71 1.06 0.78 0.64 1.41
48
CA 02 8935 98 2015-06-05
2013 Average
, ________________________________________________________________________
c >,
.,
--E-. '5
- Lo '->.
= --- Ego F a.. a 0 % -, u_
2 vE u ,s
c.), 8 g 0 t - m 5 72 c t a
..= 2
2 Z "ti- 2 -2 'II- . ..z, 12 89. eL + . L)
I- - (2, m - - õ, ,i, , '..) c' o- 6
. z
0
I I 0 ! 0
PV 200 CL 2X 27.3 98.4 1 0 46.4 117.1 98.8
48.2 44.6 92.9 13 4
PV 200 CL WF 27.8 0 0 46.2 120.4 98.2 48.2
44.5 92.8 13 4
'
CV% 12.2 109 267.7 2.6 6.4 1.7 2.4 2.9
1.0 10.1 79.4
LSD (0.05) 3.0 2 0.9 1.0 7.3 1.6 1.1 1.30
0.90 1.2 3.7
. _
SE 1.04 0.50 0.4 0.4
2.55 0.57 0.4 0.42 0.28 0.42 1.34
,
,
Locations 4 4 4 4 4 4 4 4 4 4 4
2014 Vegreville, AB 2VGH
a, a,
..6
E' (a
>, .c o -g -E i '0'16
-=>,
_c
a) ? -6- 2 LL
a, a) 0 3 a) 0 (3 IL ... g 5 l',5'
,;.2. a
72 ,,,, .- 2 r,,j .- 0
_c 2
.cr) .2 0- +
> 2 W - ,;`,' .<2 -0 -a .<2 ,:, -a , 0
I- ---- .0 0_ _0 0. >., a)
s- 0 as ,-, as co i 0
>, - c)
a 7 7 g iS
0 CI
100.
PV 200 CL 2X 28.9 104. 4 0 53.0 130.0 47.6
48.2 95.7 12 4
7 0
PV 200 CL VVF 27.6 0 0 53.0 138.0 99.0 46.2
49.8 96.0 13 3
CV% 6.50 59 0.9
4.3 1.3 1.80 1.60 0.70 7.5 35.5
LSD (0.05) 2.90 2 1.0 9.0 2.0 1.60 1.30
1.30 1.8 2.2
SE 1.06 0.71 0.00 2.83 0.71
0.57 0.42 0.42 0.64 0.78
10
49
CA 028935 98 2015-06-05
2014 Carman, MB 3CRY
L., _, L., _, 1 >, ,-:,='
E Cu = u) = 0 =
.a o 0 'E. o 0 0 -E' 5 c 2 Lo =
-
>,
>, a; ...... 0 Cu- ' (T)
E .1)).
a) 0- -2 a) 0 -ro a) 0 i LL ci. 2 5
.c (1) o >, 0 ts >, 0 0 2
cs Cu 0 2
> 2 32a) .)- 10.472 +9 =ao. .11',=> +9 =ao. to .,T
2 Z:`,9 (1. +
I- .- c) ozs ,- =,- as ,,,'" r u)
>, ,:'', 3 -S' ..
LI
a, 0.1
0 0)
I I 0 0
3. 0
PV 200 CL 2X 30.0 90.4 2 0 55.0 133.0 1 0 49.0
48.4 97.4 13 11
PV 200 CL WE 33.2 o 0 55.0 138.0
103.48.6 49.2 97.8 14 12
0
. .
CV% 9.5 74 111.5 3.4 8.0 1.0 1.50 2.00 0.80 5.2 48.8
LSD (0.05) 6.1 2 1.0 3.0 21.0 2.0 1.20 1.50
1.30 1.3 7.2
SE 2.12 0.71 0.71 1.41 7.07 0.71 0.42 0.57 0.42 0.42 2.55
2014 Average
a^ ...., a' õ... if) >,
=,- ..;-*
S
'. al -g. c ., 0
E ;.,
>, = --, .E. 8_ .o E 8_ .o o (.) Cu .(T) -
06 .c
.a) ? -Cr 7L) -", 2 'Di>. 8 LL 3 15 2 a
'a Iii -o .- 72 = 7L:1 0 = - o .- a.
.4-50a, .2 ?,== a- + 2
> 2 ...C-2 -0 fa 0 ..0 12
I- -2 c) <1,- -2 a >, (I) - C)
>,
0 6 c.)
µ.':' . ca
I I 0 a
PV 200 CL 2X 29.5 97.0 3 0 54.0 132.0
102.48.3 48.3 96.6 13 7
0
101.
PV 200 CL WF 30.4 0 0 54.0 138.0 47.4
49.5 96.9 13 8
0
CV% 9.1 120 99.2 2.7 6.1 1.3 1.8 1.9
0.8 6.7 50.8
LSD (0.05) 3.8 3 1.0 2.0 10.0 2.0 1.1 1.00 1.00
1.1 3.8
SE 1.34 0.71 0.00 0.71 3.54 0.71 0.35 0.35 0.35 0.42 1.34
Locations 2 2 2 2 2 2 2 2 2 2 2
20
CA 028935 98 2015-06-05
2 Year Average
'<f)
..?-. C c
c a.0 0 .s
. W. u_ E 6 .g ;
.2
(1,.R 32 (1,9. o 2
6-c! -0 a .2 -0 a (,) .2, - +
>- - 0- .0 0- 0) co L.- N- (13 >,
a) (NJ
0
PV 200 CL 2X 28.0 97.6 2.0 0.0 49.0 122.0
99.6 48.3 45.8 94.1 12.0 5.0
PV 200 CL INF 28.7 0.0 0.0 48.7 126.2 99.1
47.9 46.4 94.3 13.0 6.0
CV% 11.2 116.8 163.4 2.7 6.3 1.6 2.2 2.6
0.9 8.8 68.5
LSD (0.05) 2.34 1.80 1.33 1.54 3.69 1.71 1.38
1.46 1.25 1.47 2.60
SE 0.84 0.65 0.48 0.55 1.33 0.62 0.50 0.53 0.45 0.53 0.94
Locations 6 6 6 6 6 6 6 6 6 6 6
Example 2. Miscellaneous Disease Resistance
Blackleg
Blackleg tolerance was measured following the standard procedure
described in the Procedures of the Western Canada Canola/Rapeseed
Recommending Committee (WCC/RRC) Incorporated for the Evaluation and
Recommendation for Registration of Canola/Rapeseed Candidate Cultivars in
Western Canada. Blackleg was rated on a scale of 0 to 5: a plant with zero
rating
is completely immune to disease while a plant with "5" rating is dead due to
blackleg infection.
Canola variety "Westar" was included as an entry/control in each blackleg
trial. Tests are considered valid when the mean rating for Westar is greater
than
or equal to 2.6 and less than or equal to 4.5. (In years when there is poor
disease
development in Western Canada the WCC/RRC may accept the use of data from
trials with a rating for Westar exceeding 2Ø)
51
CA 028935 98 2015-06-05
The ratings are converted to a percentage severity index for each line, and
the following scale is used to describe the level of resistance:
Classification Rating (% of Westar)
R (Resistant) <30
MR (Moderately Resistant) 30 ¨ 49
MS (Moderately Susceptible) 50 ¨ 69
S (Susceptible) 70 ¨ 89
HS (Highly Susceptible) 90 - 100
Table 3. Summary of Blackleg Ratings for PV 200 CL
2014
.c
-0 C 0 o iT1
0 o
_0
16 w o
>- () >-
0
< ZL
co co
PV 200 CL 1.27 0.84 0.57 0.96 1.85 1.03 1.1 29.1
R
Westar 4.36 3.25 2.93 4.43 4.12 3.05 3.7 100.0
Example 3: Summary of Performance of PV 200 CL in two years of Co-op
Testi na
Two years (2013 and 2014) of trials were conducted. WCC/RRC guidelines
were followed for conducting trials. Each trial had three replicates and had a
plot
size of 1.5m x 6m. Yield and agronomic traits were recorded and seed samples
were collected from two of the three replicates at selected sites and were
analyzed
for quality traits such as oil and protein percent at 8.5% moisture, total
whole seed
glucosinolates at 8.5%, chlorophyll, total saturated fatty acid, 1000 seed
weight etc.
WCC/RRC guidelines were followed for analyzing quality parameters.
52
CA 02 8935 98 2015-06-05
Table 4. Summary of Performance of PV 200 CL in two years of Co-op Testing
2 '6
tu)) ,-'-,' zr, 2 17, f 5i i 1-6
0 IL. -a
z i 14'
-03
0
0 0
.c = 3 o 2 - - CD LI
a
E
^ E )--'' -ra 2 (63 A ._e. -- 3 2 2
0
a) s. , '
co _ - - "5
.2
CU Cr -cl 0 M LI- ci, .0) a) '5, , (L, w
0 2. c --= z7
a
> >Ct 0 0 5 - o 2 N
01 0 ,, .S 3 (1) 5 2 cn
'a' w.i) a) .(2 2
( ' TV Ta z 0
.... a.
5- o_ 0 ti o 0
I- 03
2013
PV 200
25.0 99.5 99.6 48.0 7.0 119.0 49.3 43.3 92.6 6.4 12.0
CL
45H29 24.7 98.2 98.4 46.0 6.4 118.0 49.5 44.8 94.3 6.6 14.0
5440 25.6 101.8 98.5 46.0 7.6 120.0 48.3 44.0 92.3 6.4 12.6
CHK
AVG 25.1 100.0 98.5 460 7.0 119.0 48.9 44.4 93.3 6.5 13.3
Loc 19 19 15 8 9 12 18 18 18 18 18
,
Diff -0.1 -0.5 1.1 2.0 0.0 0.0 0.4 -1.1 -0.7
0.0 -1.3
2014
PV 200
35.0 100.5 95.0 47.0 7.3 115.0 47.9 44.9 92.8 6.5 9.7 7.3 29.1
CL
45H29 34.6 99.4 93.4 45.0 7.2 116.0 48.7 45.5 94.2 6.6 12.4 6.3 43.3
5440 35.1 100.6 94.0 46.0 7.8 116.0 47.3 44.9 92.2 6.4 10.1 5.4 58.6
CHK
AVG 34.8 100.0 93.7 45.5 7.5 116.0 48.0 45.2 93.2 6.5 11.2 5.9 51.0
Loc 16 13 11 16 13 13 13 13 13 6 6
Diff 0.2 0.5 1.3 1.5 -0.2 -1.0 -0.1 -0.3 -0.4
0.0 -1.5 1.5
2 Year
Avg
PV 200
30.0 100.0 97.3 47.5 7.2 117.0 48.6 44.1 92.7 6.4 10.8
CL
45H29 29.6 98.8 95.9 45.5 6.8 117.0 49.1 45.2 94.3 6.6 13.2
5440 30.3 101.2 96.3 46.0 7.7 118.0 47.8 44.4 92.2 6.4 11.3
53
CA 02893598 2015-06-05
_
CHK
30.0 100.0 96.1 45.8 7.3 117.5 48.4 44.8 93.2 6.5 12.2
AVG
Loc 35 19 28 19 25 25 31 31 18 31 31
Diff 0.0 0.0 1.2 1.8 -0.1 -0.5 0.1 -0.7 -0.5
0.0 -1.4
The foregoing invention has been described in detail by way of illustration
and
example for purposes of exemplification. However, it will be apparent that
changes
and modifications such as single gene modifications and mutations, somaclonal
variants, variant individuals selected from populations of the plants of the
instant
variety, and the like, are considered to be within the scope of the present
invention.
The scope of the claims should not be limited by the preferred embodiments set
forth in the examples, but should be given the broadest interpretation
consistent
to with the description as a whole.
54
