Claims for Patent: 8,975,471

Summary for Patent: 8,975,471

Title:	MicroRNAs
Abstract:	The invention provides methods and compositions useful in target sequence suppression, target sequence validation and target sequence down regulation. The invention provides polynucleotide constructs useful for gene silencing or RNA down regulation, as well as cells, plants and seeds comprising the polynucleotides. The invention also provides a method for using microRNA to silence a target sequence or to down regulate RNA.
Inventor(s):	Reyes Taboada; Jose L. (Mexico City, MX), Zhang; Xiuren (New York, NY), Soyano; Takashi (New York, NY), Chua; Nam-Hai (New York, NY), Niu; Qi-Wen (Staten Island, NY), Lin; Shih-Shun (New York, NY)
Assignee:	The Rockefeller University (New York, NY)
Application Number:	11/247,587
Patent Claims:	1. A method of obtaining a disease resistant plant by down regulating a target sequence of a plant virus or plant viroid in a plant, consisting of: (a) transforming a plant cell susceptible to infection by the plant virus or plant viroid with a nucleic acid construct comprising a promoter functional in a plant cell operably linked to a polynucleotide, wherein the polynucleotide encodes one or more modified miRNA precursors, wherein each modified miRNA precursor comprises a fragment of a plant miRNA primary transcript that is modified in the miRNA sequence and the miRNA complementary sequence, wherein the plant miRNA primary transcript is a plant miR159 primary transcript, further wherein each modified miRNA precursor is capable of forming a first double-stranded RNA or a hairpin, wherein each modified miRNA is an miRNA modified to be (i) fully complementary to a target sequence, (ii) fully complementary to a target sequence except for GU base pairing or (iii) fully complementary to a target sequence in the first ten nucleotides counting from the 5' end of the miRNA, wherein the target sequence of each modified miRNA is the same or different, and wherein at least one target sequence encodes a gene silencing suppressor of a plant virus or plant viroid and wherein the modified miRNA sequence targeting said gene silencing suppressor consists of (i) the nucleotide sequence of SEQ ID NO:162 or (ii) a nucleotide sequence that is at least 90% identical to the nucleotide sequence of SEQ ID NO:162; (b) obtaining a transgenic plant from the transformed plant cell of (a); (c) expressing the nucleic acid construct in the transgenic plant of (b) for a time sufficient to produce each modified miRNA, wherein each modified miRNA binds to its target sequence to form a second double-stranded RNA which is cleaved thereby down regulating the target sequence; and (d) selecting a transgenic plant of (c) that is resistant to a plant virus or plant viroid, wherein the plant virus or plant viroid comprises the at least one target sequence that encodes the gene silencing suppressor and wherein the resistant transgenic plant shows no symptoms of infection. 2. The method of claim 1, wherein the cell is from a plant selected from the group consisting of corn, wheat, rice, barley, oats, sorghum, millet, sunflower, safflower, cotton, soy, canola, alfalfa, Arabidopsis, and tobacco. 3. The method of claim 1, wherein the modified miRNA is a plant miRNA modified to be fully complementary to the target sequence. 4. The method of claim 1, wherein the promoter is a pathogen-inducible promoter. 5. The method of claim 1, wherein the nucleic acid construct encodes two or more modified miRNA precursor sequences. 6. The method of claim 5, wherein the nucleic acid construct encodes a hetero-polymeric precursor miRNA or a homo-polymeric precursor miRNA. 7. The method of claim 1, wherein the nucleic acid construct is inserted into an intron of a gene or transgene of the plant cell. 8. The method of claim 3, wherein the cell is from a plant selected from the group consisting of corn, wheat, rice, barley, oats, sorghum, millet, sunflower, safflower, cotton, soy, canola, alfalfa, Arabidopsis, and tobacco. 9. The method of claim 2, wherein the plant miRNA is from a plant selected from the group consisting of Arabidopsis, tomato, soybean, rice, and corn. 10. The method of claim 3, wherein the promoter is a pathogen-inducible promoter. 11. The method of claim 3, wherein the nucleic acid construct encodes two or more modified miRNA precursor sequences. 12. The method of claim 4, wherein the nucleic acid construct encodes two or more modified miRNA precursor sequences. 13. The method of claim 1, wherein the nucleotide sequence (ii) is at least 95% identical to the nucleotide sequence of SEQ ID NO:162. 14. The method of claim 13, wherein the nucleic acid construct encodes two or more modified miRNA precursor sequences. 15. The method of claim 11, wherein the nucleic acid construct encodes a hetero-polymeric precursor miRNA or a homo-polymeric precursor miRNA. 16. The method of claim 12, wherein the nucleic acid construct encodes a hetero-polymeric precursor miRNA or a homo-polymeric precursor miRNA. 17. The method of claim 14, wherein the nucleic acid construct encodes a hetero-polymeric precursor miRNA or a homo-polymeric precursor miRNA. 18. The method of claim 3, wherein the nucleic acid construct is inserted into an intron of a gene or transgene of the cell. 19. The method of claim 4, wherein the cell is from a plant selected from the group consisting of corn, wheat, rice, barley, oats, sorghum, millet, sunflower, safflower, cotton, soy, canola, alfalfa, Arabidopsis, and tobacco. 20. The method of claim 4, wherein the nucleic acid construct is inserted into an intron of a gene or transgene of the cell. 21. The method of claim 5, wherein the cell is from a plant selected from the group consisting of corn, wheat, rice, barley, oats, sorghum, millet, sunflower, safflower, cotton, soy, canola, alfalfa, Arabidopsis, and tobacco. 22. The method of claim 6, wherein the cell is from a plant selected from the group consisting of corn, wheat, rice, barley, oats, sorghum, millet, sunflower, safflower, cotton, soy, canola, alfalfa, Arabidopsis, and tobacco. 23. The method of claim 5, wherein the nucleic acid construct is inserted into an intron of a gene or transgene of the cell. 24. The method of claim 7, wherein the cell is from a plant selected from the group consisting of corn, wheat, rice, barley, oats, sorghum, millet, sunflower, safflower, cotton, soy, canola, alfalfa, Arabidopsis, and tobacco. 25. The method of claim 13, wherein the cell is from a plant selected from the group consisting of corn, wheat, rice, barley, oats, sorghum, millet, sunflower, safflower, cotton, soy, canola, alfalfa, Arabidopsis, and tobacco. 26. The method of claim 13, wherein the promoter is a pathogen-inducible promoter. 27. The method of claim 13, wherein the nucleic acid construct is inserted into an intron of a gene or transgene of the cell. 28. The method of claim 8, wherein the plant miRNA is from a plant selected from the group consisting of Arabidopsis, tomato, soybean, rice, and corn. 29. The method of claim 19, wherein the plant miRNA is from a plant selected from the group consisting of Arabidopsis, tomato, soybean, rice, and corn. 30. The method of claim 21, wherein the plant miRNA is from a plant selected from the group consisting of Arabidopsis, tomato, soybean, rice, and corn. 31. The method of claim 22, wherein the plant miRNA is from a plant selected from the group consisting of Arabidopsis, tomato, soybean, rice, and corn. 32. The method of claim 24, wherein the plant miRNA is from a plant selected from the group consisting of Arabidopsis, tomato, soybean, rice, and corn. 33. The method of claim 25, wherein the plant miRNA is from a plant selected from the group consisting of Arabidopsis, tomato, soybean, rice, and corn.

Details for Patent 8,975,471

Applicant	Tradename	Biologic Ingredient	Dosage Form	BLA	Approval Date	Patent No.	Expiredate
Merck Sharp & Dohme Corp.	INTRON A	interferon alfa-2b	For Injection	103132	06/04/1986		2039-02-26
Merck Sharp & Dohme Corp.	INTRON A	interferon alfa-2b	For Injection	103132			2039-02-26
Merck Sharp & Dohme Corp.	INTRON A	interferon alfa-2b	Injection	103132			2039-02-26