Methods and compositions for weed control

Patent metadata

Field	Value
Publication number	US-9422558-B2
Application number	US-201213612948-A
Country	US
Kind code	B2
Filing date	Sep 13, 2012
Priority date	Sep 13, 2011
Publication date	Aug 23, 2016
Grant date	Aug 23, 2016

Abstract

The present invention provides novel compositions for use to enhance weed control. Specifically, the present invention provides for methods and compositions that modulate glutamine synthetase in weed species. The present invention also provides for combinations of compositions and methods that enhance weed control.

First claim

We claim:

1. A method of plant control comprising: treating a plant with a composition comprising a non-transcribable polynucleotide and a transfer agent, wherein said non-transcribable polynucleotide is from 18 to about 700 nucleotides in length and is at least 85% identical or at least 85% complementary to a glutamine synthetase (GS) gene sequence or to an RNA transcript of said GS gene sequence, wherein said GS gene sequence is selected from the group consisting of SEQ ID NOs:1-59 and a polynucleotide fragment thereof, wherein said transfer agent conditions the surface of said plant for permeation by said non-transcribable polynucleotide, and whereby said plant's growth, development, or reproductive ability is suppressed or delayed or said plant is more sensitive to a GS inhibitor herbicide as a result of said non-transcribable polynucleotide containing composition relative to a plant not treated with said composition.

2. The method as claimed in claim 1 , wherein said transfer agent is an organosilicone surfactant composition or compound contained therein.

3. The method as claimed in claim 1 , wherein said non-transcribable polynucleotide is selected from the group consisting of sense ssDNA, anti-sense ssDNA, sense ssRNA, anti-sense ssRNA, dsRNA, dsDNA, and dsDNA/RNA hybrids.

4. The method as claimed in claim 1 , wherein said plant is selected from the group consisting of Abutilon theophrasti, Amaranthus albus, Amaranthus chlorostachys, Amaranthus graecizans, Amaranthus hybridus, Amaranthus lividus, Amaranthus palmeri, Amaranthus rudis, Amaranthus spinosus, Amaranthus thunbergii, Ambrosia trifida, Ambrosia artemisiifolia, Chenopodium album, Commelina diffusa, Convulvulus arvensis, Conyza candensis, Lolium multiflorum, Euphorbia heterophylla, Kochia scoparia, Sorghum halepense and Digitaria sanguinalis.

5. The method as claimed in claim 1 , wherein said composition further comprises said GS inhibitor herbicide and said treating comprises external application to said plant with said composition.

6. The method as claimed in claim 5 , wherein said composition further comprises one or more co-herbicides similar or different from said GS inhibitor herbicide.

7. The method as claimed in claim 1 , wherein said composition comprises any combination of two or more of said non-transcribable polynucleotide or a fragment thereof and said treating comprises external application to said plant with said composition.

8. A composition comprising a non-transcribable polynucleotide and a transfer agent, wherein said non-transcribable polynucleotide is from 18 to about 700 nucleotides in length and is at least 85% identical or at least 85% complementary to a GS gene sequence, or to an RNA transcript of said GS gene sequence, wherein said GS gene sequence is selected from the group consisting of SEQ ID NOs:1-59 and a polynucleotide fragment thereof, wherein said transfer agent conditions the surface of a plant for permeation by said non-transcribable polynucleotide, and whereby said plant treated with said composition has its growth, development, or reproductive ability suppressed or delayed or said plant is more sensitive to a GS inhibitor herbicide as a result of said non-transcribable polynucleotide containing composition relative to a plant not treated with said composition.

9. The composition of claim 8 , wherein said transfer agent is an organosilicone composition.

10. The composition of claim 8 , wherein said non-transcribable polynucleotide is selected from the group consisting of SEQ ID NOs:60-1443 and a fragment thereof.

11. The composition of claim 8 , wherein said non-transcribable polynucleotide is selected from the group consisting of SEQ ID NOs: 1444-2045 and a fragment thereof.

12. The composition of claim 8 , further comprising said GS inhibitor herbicide.

13. The composition of claim 12 , wherein said GS inhibitor herbicide is selected from the group consisting of glufosinate-ammonium and bialaphos.

14. The composition of claim 12 , further comprising a co-herbicide.

15. A method of reducing expression of a GS gene in a plant comprising: external application to said plant of a composition comprising a non-transcribable polynucleotide and a transfer agent, wherein said non-transcribable polynucleotide is from 18 to about 700 nucleotides in length and is at least 85% identical or at least 85% complementary to a GS gene sequence or to an RNA transcript of said GS gene sequence wherein said GS gene sequence is selected from the group consisting of SEQ ID NOs:1-59 and a polynucleotide fragment thereof, wherein said transfer agent conditions the surface of said plant for permeation by said non-transcribable polynucleotide, and whereby said expression of said GS gene is reduced relative to a plant in which the composition was not applied.

16. The method as claimed in claim 15 , wherein said transfer agent is an organosilicone compound.

17. The method as claimed in claim 15 , wherein said non-transcribable polynucleotide is selected from the group consisting of sense ssDNA, anti-sense ssDNA, sense ssRNA, anti-sense ssRNA, dsRNA, dsDNA, and dsDNA/RNA hybrids.

18. A method of identifying non-transcribable polynucleotides useful in modulating GS gene expression when externally treating a plant comprising: a) providing a plurality of non-transcribable polynucleotides that are from 18 to about 700 nucleotides in length and are at least 85 percent identical or at least 85 percent complementary to a GS gene sequence selected from the group consisting of SEQ ID NOs:1-59; b) externally treating said plant with one or more of said non-transcribable polynucleotides and a transfer agent; and c) analyzing said plant or extract for modulation of GS gene expression, wherein said transfer agent conditions the surface of said plant for permeation by said one or more of said non-transcribable polynucleotides, and whereby said plant treated with said one or more of said non-transcribable polynucleotides and said transfer agent has its growth, development, or reproductive ability suppressed or delayed or said plant is more sensitive to a GS inhibitor herbicide as a result of said one or more of said non-transcribable polynucleotides and said transfer agent relative to a plant not treated with said one or more of said non-transcribable polynucleotides and said transfer agent.

19. The method as claimed in claim 18 , wherein said plant is selected from the group consisting of Abutilon theophrasti, Amaranthus albus, Amaranthus chlorostachys, Amaranthus graecizans, Amaranthus hybridus, Amaranthus lividus, Amaranthus palmeri, Amaranthus rudis, Amaranthus spinosus, Amaranthus thunbergii, Ambrosia trifida, Ambrosia artemisiifolia, Chenopodium album, Commelina diffusa, Convulvulus arvensis, Conyza candensis, Lolium multiflorum, Euphorbia heterophylla, Kochia scoparia, Sorghum halepense and Digitaria sanguinalis.

20. The method as claimed in claim 18 , wherein said GS gene expression is reduced relative to a plant not treated with said one or more of said non-transcribable polynucleotides and said transfer agent.

21. The method as claimed in claim 18 , wherein said transfer agent is an organosilicone compound.

22. An agricultural chemical composition comprising an admixture of a non-transcribable polynucleotide, a GS inhibitor herbicide, and a co-herbicide, wherein said non-transcribable polynucleotide is from 18 to about 700 nucleotides in length and is at least 85% identical or at least 85% complementary to a portion of a GS gene

Assignees

• Ader Daniel
• Fiinnessy John J
• Li Zhaolong
• Masucci James D
• Shah Ronak Hasmukh
• Tao Nengbing
• Taylor Jennifer Chou
• Monsanto Technology Llc

Inventors

• Ader Daniel
• Fiinnessy John J
• Li Zhaolong
• Masucci James D
• Shah Ronak Hasmukh
• Tao Nengbing
• Taylor Jennifer Chou

Classifications

• C12Y603/01006

  Glutamate--ethylamine ligase (6.3.1.6) · CPC title

• C12N9/93 Primary

  Ligases (6) · CPC title

• C12N15/8251

  Amino acid content, e.g. synthetic storage proteins, altering amino acid biosynthesis · CPC title

• C12N15/8218

  Antisense, co-suppression, viral induced gene silencing [VIGS], post-transcriptional induced gene silencing [PTGS] · CPC title

• A01N57/20

  containing acyclic or cycloaliphatic radicals · CPC title