专利摘要:
  RECOMBINANT DNA MOLECULES, METHODS AND KIT FOR THEIR DETECTION, MICROORGANISM AND PRODUCT UNDERSTANDING SUCH MOLECULES, METHODS FOR THE CONTROL OF WEEDS, FOR THE PRODUCTION OF SOYBEAN SEED AND A SOYBEAN PLANT, AS WELL AS DEEIN PLANT .The present invention relates to a MON 87708 transgenic soybean event plant and plants, plant cells, seeds, plant parts and products derived from the MON 87708 event. The invention also relates to specific polynucleotides for the MON 87708 event and plants , plant cells, seeds, plant parts and products comprising polynucleotides specific for the MON 87708 event. The invention also provides methods related to the MON 87708 event.
公开号:BR112012006079A2
申请号:R112012006079-1
申请日:2010-08-26
公开日:2021-02-02
发明作者:Ronald J. Brinker;Wen C. Burns;Paul C. C. Feng;Anju Gupta;Sio-Wai Hoi;Marianne Malven;Kunsheng Wu
申请人:Monsanto Technology Llc;
IPC主号:
专利说明:

Invention Patent Descriptive Report for "MOLECULES .. OF RECOMBINANT DNA, METHODS AND KIT FOR ITS DETECTION, MICROORGANISM AND PRODUCT UNDERSTANDING SUCH MOLECULES, METHODS FOR THE CONTROL OF WEED, FOR SEED AND SEED PLANT OF SOYBEAN, AS WELL AS DETERMINING THE ZYGOSITY OF A PLANT OR SEED ".
CROSS REFERENCE TO RELATED APPLICATIONS This patent application claims the benefit of Provisional Patent Application U.S No. 61 / 243,227 filed on September 17, 2009, which is incorporated in this application by reference in its entirety.
SEQUENCE LISTING INCORPORATION The sequence listing that is contained in the file named "55544-0001 sedqlisting.txt", which is 19.5 kilobytes (size measured in Microsoft Windows ) And was created on August 13, 2010, it is deposited by electronic submission and is incorporated by reference in this order.
FIELD OF THE INVENTION The invention relates to the transgenic event of Glycine max MON 87708. The event exhibits tolerance to the herbicide dicamba. The invention also relates to plants, plant parts, plant seeds, plant cells, agricultural products and methods related to the MON 87708 event and provides nucleotide molecules that are unique to the event and were created due to the insertion of transgenic DNA in the genome of a Glycinemax plant.
BACKGROUND OF THE INVENTION Soy (Glycine max) is an important crop in many areas of the world and methods of biotechnology have been applied to this crop in order to produce soybeans with desirable traits. Such a desirable trait is tolerance to herbicides. The expression of a herbicide tolerance transgene in a plant can confer the desirable trait of herbicide tolerance in the plant, but the expression of the transgene can be influenced by the chromium position.
1a / 44 and the genomic result of the transgene insertion.
For example, it has been observed in plants that there is often variation in the level and pattern of transgenic expression between individual events that differ at the chromosomal insertion site of the transgene, but are identical.
There may also be undesirable and / or desirable phenotypic or agronomic differences.
权利要求:
Claims (30)
[1]
CLAIMS O 1. Recombinant DNA molecule, characterized by the fact that it comprises a nucleotide molecule comprising a nucleotide sequence selected from the group consisting of SEQ ID NO: 1-8, and components thereof.
[2]
2. Recombinant DNA molecule according to claim 1, characterized by the fact that it is formed by the insertion of a heterologous nucleic acid molecule in the genomic DNA of a soybean plant, plant cell or seed.
[3]
3. Recombinant DNA molecule according to claim 1, characterized by the fact that it is derived from the MON 87708 transgenic soy event, a representative sample of which deposited as ATCC PTA-9670.
[4]
4. Recombinant DNA molecule according to claim 1, characterized by the fact that said DNA molecule is in a soy plant, plant cell, seed, plant part, or product derived from the MON 87708 soy event, a representative sample of which deposited as ATCC PTA-9670.
[5]
5. Recombinant DNA molecule according to claim 1, characterized by the fact that said DNA molecule is an amplicon diagnosis of the presence of DNA derived from the MON 87708 event.
[6]
6. DNA molecule, characterized by the fact that it comprises a nucleotide molecule having a nucleotide sequence of sufficient length of the contiguous nucleotide sequence of SEQ ID NO: 6, and complements thereof, to function as a DNA probe that - bridles under stringent hybridization conditions with a DNA molecule comprising a nucleotide sequence selected from the group consisting of SEQ ID NO: 1-8 and does not hybridize under stringent hybridization conditions with a DNA molecule not comprising a nucleotide sequence selected from the group consisting of SEQ ID NO: 1-8.
[7]
7. Pair of DNA molecules, characterized by the fact that it consists of a first DNA molecule and a second DNA molecule - different from the first DNA molecule, in which the said first and second DNA molecule each comprises a A nucleotide molecule containing a nucleotide sequence of sufficient length of contiguous nucleotides of SEQ ID NO: 6, or a complement to it, to function as DNA primers when used together in an amplification reaction with DNA derived from MON 87708 event to produce an amplicon diagnosis for MON 87708 soy event DNA in a sample.
[8]
8. Method of detecting the presence of a DNA molecule derived from the MON 87708 soy event in a sample, characterized by the fact that it comprises: a. contacting a sample with the DNA probe as defined in claim 6; B. subjecting said sample and said DNA probe to stringent hybridization conditions; and c. detecting the hybridization of said DNA probe to a DNA molecule in said sample, wherein the hybridization of said DNA probe to said DNA molecule indicates the presence of a DNA molecule derived from the soybean event MON 87708 in said sample.
[9]
9. Method for detecting the presence of a DNA molecule derived from the MON 87708 soy event in a sample, characterized by the fact that it comprises: a. contacting a sample with the pair of DNA molecules co-defined in claim 7; B. carrying out an amplification reaction sufficient to produce DNA amplicon comprising a sequence selected from the group consisting of SEQ ID NO: 1-8, and complements thereof; and c. detection of the presence of said DNA amplicon in said reaction, in which the presence of said DNA amplicon in said reaction indicates the presence of a DNA molecule derived from the MON 87708 soy event in said sample.
[10]
10. DNA detection kit, characterized by the fact that .. comprises at least one DNA molecule comprising a nucleotide sequence of sufficient length of the contiguous nucleotide sequence of SEQ ID NO: 6, and complements thereof, to function as a specific DNA primer or probe for detecting the presence of DNA derived from the MON 87708 soy event, in which the detection of said DNA is diagnostic for the presence of said MON 87708 event DNA in a sample.
[11]
11. Recombinant soybean plant, seed, cell, or vegetable part, characterized by the fact that it comprises a nucleotide molecule having a nucleotide sequence selected from the group consisting of SEQ ID NO: 1-8, and complements thereof .
[12]
12. Recombinant soybean plant, seed, cell, or plant part according to claim 11, characterized by the fact that when adding plant, seed, cell or plant part of it is tolerant to treatment with dicamba herbicide .
[13]
13. Recombinant soybean plant, seed, cell, or plant part thereof according to claim 11, characterized by the fact that its genome produces an amplicon comprising a DNA molecule selected from the group consisting of SEQ ID NO : 1-8, and complements to it, when tested in a DNA amplification method.
[14]
14. Soybean plant or seed, characterized by the fact that it contains MON 87708 soybean event, a representative sample of which deposited under ATCC Accession No. PTA-9670.
[15]
15. Soybean plant or seed according to claim 14, characterized by the fact that it is a hybrid having at least one parent derived from the MON 87708 soybean event.
[16]
16. Non-living plant material, characterized by the fact that it comprises a recombinant DNA molecule selected from the group consisting of SEQ ID NO: 1-8, and complementary to it.
[17]
17. Microorganism, characterized by the fact that it comprises
of a nucleotide molecule having a selected nucleotide sequence and nothing from the group consisting of SEQ ID NO: 1-8, and complementary thereto.
[18]
18. Microorganism according to claim 17, characterized by the fact that said microorganism is a plant cell.
[19]
19. Product, characterized by the fact that it comprises a nucleotide molecule having a nucleotide sequence selected from the group consisting of SEQ ID NO: 1-8, and complementary thereto.
[20]
20. Product according to claim 19, characterized by the fact that it is selected from the group consisting of whole or processed seeds, fodder, oil, fine flour, flour, flakes, cherry bran, milk, cheese, paper, cream, wine, biomass and fuel products.
[21]
21. Method for controlling weeds in a field, characterized by the fact that it comprises planting the MON 87708 soy event plants in a field and applying an effective dose of the herbicide dicamba to control weeds in the field. said field without harming said plants of the MON 87708 soy event.
[22]
22. Method according to claim 21, characterized by the fact that said effective dose of the dicamba herbicide is approximately 5.68 g / ha (0.005 pounds / acre) to approximately 8,970 g / ha (8 | i - bras / acre).
[23]
23. Method for controlling weeds in a field, characterized by the fact that it comprises the application of an effective dose of the herbicide dicamba to control weeds in a field and then planting the MON 87708 soy event in that field.
[24]
24. Method according to claim 23, characterized by the fact that said effective dose of the dicamba herbicide is approximately 5.68 g / ha (0.005 pounds / acre) to approximately 8,970 g / ha (8 pounds) / acre) and implantation of MON 87708 soy event is within 14 days of the said application of an effective dose of the herbicide dicamba.
[25]
25. Method for the production of soy seed essentially without seeds of toxic weed species, characterized by: the fact that it comprises: a. planting seeds from the MON 87708 soy event in a field; B. application of an effective dose of a dicamba herbicide to this field to eliminate toxic weeds in said field without harming said plants of the MON 87708 soy event; and c. harvesting of soybean seed from said field.
[26]
26. Method according to claim 25, characterized by the fact that the seeds of said toxic weed species are selected from the group consisting of Cardaria spp, Heliotropium spp, Centaurea spp., Senecio spp., Crotalaria spp., Solanum spp., Xanthium spp., Amsinckia spp., Cassia spp., Sesbania spp., Datura spp., Ricinus Spp., Argemone spp., Corchorus spp., Impomoea spp., And Echium spp.
[27]
27. Method of production of a soybean plant that tolerates the application of the herbicide dicamba, characterized by the fact that it comprises: a. sexual crossover of a MON 87708 transgenic soybean event plant comprising a nucleotide molecule having a nucleotide sequence selected from the group consisting of SEQID NO: 14, and complements thereof, with a second soybean plant; B. collecting the seed produced from said crossing; CC. growing said seed to produce a plurality of progeny plants; d. treatment of said plurality of progeny plants with dipamba; and is. selection of a progeny plant that is tolerant to dicamba.
[28]
28. Method of production of a soybean plant that tolerates the application of the herbicide dicamba, characterized by the fact that it comprises: a. self-pollination of a MON 87708 transgenic soybean event plant comprising a nucleotide molecule having a nucleotide sequence selected from the group consisting of SEQ ID
NO: 1-8, and complements to it; : B. collecting the seed produced from said self-pollination; CC. growing said seed to produce a plurality of progeny plants; d. treatment of said plurality of progeny plants with dipamba; and is. selection of a progeny plant that is tolerant to dicamba.
[29]
29. Method of determining the zygosity of a plant from the MON 87708 soybean event or seed, characterized by the fact that it comprises: a. contacting the sample comprising the soybean DNA with a set of primers comprising SEQ ID NO: 12, SEQ ID NO: 13, and SEQ ID NO: 14 and a set of probes comprising SEQ ID NO: 15 and SEQ ID NO: 16; B. carrying out a nucleic acid amplification reaction with said sample, set of primers, and set of probes; ç. detection in said nucleic acid amplification reaction of a first fluorescent signal that is diagnostic for the MON 87708 event and a second fluorescent signal different from said first fluorescent signal and diagnosis for genomic DNA of native soybean corresponding to the position of the transgene insertion the MON 87708 event; and d. analysis of the presence and / or absence of said first fluorescent signal and said second fluorescent signal in said nucleic acid amplification reaction, in which the presence of both fluorescent signals indicates that said sample is heterozygous for the MON 87708 event and the presence of said first fluorescent signal only indicates that said sample is homozygous for the MON 87708 event.
[30]
30. Soy haplotype region in link group 9 approximately at the position of map 143.5, characterized by the fact that it comprises a dicamba tolerance gene and still defined by the 19743 and 19767 haplotype window.
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EP3613736A1|2018-08-22|2020-02-26|Basf Se|Substituted glutarimide derivatives|
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法律状态:
2021-02-17| B06F| Objections, documents and/or translations needed after an examination request according [chapter 6.6 patent gazette]|
2021-03-02| B06U| Preliminary requirement: requests with searches performed by other patent offices: procedure suspended [chapter 6.21 patent gazette]|
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2021-06-01| B06A| Patent application procedure suspended [chapter 6.1 patent gazette]|
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优先权:
申请号 | 申请日 | 专利标题
US24322709P| true| 2009-09-17|2009-09-17|
US61/243,227|2009-09-17|
PCT/US2010/046759|WO2011034704A1|2009-09-17|2010-08-26|Soybean transgenic event mon 87708 and methods of use thereof|
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