Methods for determining the presence or absence of elite event RF-BN1 in
This invention relates to transgenic winter oilseed rape (WOSR) plants, plant material and seeds, harboring a specific transformation event. It pertains to winter oilseed rape plants, more particularly to a pair of winter oilseed rape plants, which is particularly suited for the production of hybrid seed. More specifically, one plant is characterized by being male-sterile, due to the presence in its genome of a male sterility gene, while the other is characterized by carrying a fertility-restorer gene, capable of preventing the activity of the male-sterility gene. The invention further provides a method for producing hybrid seed, a process for producing a transgenic WOSR plant oil or plant, and a method to identify a transgenic plant, cell or tissue. A kit for identifying the transgenic plants comparing the elite event of the present invention is also described. The WOSR plants of the invention combine the ability to form hybrid seeds with optimal overall agronomic performance, genetic stability and adaptability to different generic backgrounds.
1. A kit for identifying elite event MS-BN1 in a biological sample of a Brassica plant, Brassica plant material, or a product comprising a Brassica plant material, said kit comprising at least two primers, wherein:
(a) a first primer comprises 19 consecutive nucleotides of nucleotides: 1-867 of SEQ ID NO: 13; or nucleotides 1-771 of SEQ ID NO: 36;
and a second primer comprises 19 consecutive nucleotides of the complement of: nucleotides 868-953 of SEQ ID NO: 13 or of nucleotides 772-909 of SEQ ID NO: 36, or wherein a second primer comprises 19 consecutive nucleotides of SEQ ID NO: 1 or the complement thereof; or
(b) a first primer comprises 19 consecutive nucleotides of the complement of nucleotides 181-537 of SEQ ID NO: 18 or nucleotides 181-522 of SEQ ID NO: 38;
and a second primer comprises 19 consecutive nucleotides of nucleotides 1-180 of SEQ ID NO: 18 or nucleotides 1-180 of SEQ ID NO: 38, or wherein a second primer comprises 19 consecutive nucleotides of SEQ ID NO: 1, or the complement thereof;
wherein the first and the second primer amplify a DNA fragment from a nucleic acid present in a biological sample that comprises elite event MS-BN1, and
wherein the first and the second primer do not amplify said DNA fragment from a nucleic acid present in a biological sample that does not comprise elite event MS-BN1.
2. The kit of claim 1 , wherein the first primer comprises the sequence of SEQ ID NO: 19.
3. The kit of claim 1 , wherein the second primer comprises the sequence of SEQ ID NO: 12.
4. A method for identifying elite event MS-BN1 in a biological sample of a Brassica plant, Brassica plant material, or a product comprising a Brassica plant material, which method comprises determining whether a DNA fragment is amplified from a nucleic acid present in said biological sample in a polymerase chain reaction using a kit according to any one of claim 1 , 2 or 3 .
5. The method of claim 4 , wherein the biological sample is genomic DNA from a seed sample and the method is a method for screening seeds for the presence of MS-BN1.
6. A method for identifying a transgenic Brassica plant, or cells or tissues thereof, comprising elite event MS-BN1, which method comprises determining whether a DNA fragment of between 260 and 300 base pairs is amplified from genomic DNA of the transgenic Brassica plant, or cells or tissues in a polymerase chain reaction using the kit of claim 1 , wherein the first primer comprises the sequence of SEQ ID NO: 19 and the second primer comprises the sequence of SEQ ID NO: 12, and wherein, if the DNA fragment is amplified, the Brassica plant, cells or tissues comprise elite event MS-BN1.
7. The method of claim 6 , wherein the DNA fragment is about 280 base pairs.