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Last Updated: March 28, 2024

Claims for Patent: 6,743,580


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Summary for Patent: 6,743,580
Title: Methods for producing transgenic plants containing evolutionarily significant polynucleotides
Abstract:The present invention provides methods for identifying polynucleotide and polypeptide sequences which may be associated with commercially or aesthetically relevant traits in domesticated plants or animals. The methods employ comparison of homologous genes from the domesticated organism and its ancestor to identify evolutionarily significant changes. Sequences thus identified may be useful in enhancing commercially or aesthetically desirable traits in domesticated organisms.
Inventor(s): Messier; Walter (Longmont, CO), Sikela; James M. (Englewood, CO)
Assignee: Evolutionary Genomics LLC (Aurora, CO)
Application Number:09/875,666
Patent Claims:1. A method of making a transfected plant cell or a transgenic plant comprising: a) identifying a polynucleotide sequence encoding a polypeptide of a domesticated plant, wherein said polypeptide is or is suspected of being associated with a commercially or aesthetically relevant trait that is unique, enhanced or altered in the domesticated plant as compared to a wild ancestor of said domesticated plant; and b) transfecting a plant cell with said identified polynucleotide sequence, whereby a transgenic plant may be produced.

2. The method of claim 1, further comprising, between steps (a) and (b), the step of mutating said polynucleotide.

3. The method of claim 2, wherein said mutation is produced by site-directed mutagenesis.

4. The method of claim 2, wherein said mutation is produced by random mutagenesis.

5. The method of claim 1, wherein said step (a) comprises: (i)comparing polypeptide-coding nucleotide sequences of said domesticated plant to polypeptide-coding nucleotide sequences of said wild ancestor; and (ii) selecting a polynucleotide sequence in the domesticated plant that contains a nucleotide change as compared to a corresponding sequence in the wild ancestor,

wherein said change is evolutionarily significant.

6. A method of identifying an agent which may modulate a commercially or aesthetically relevant trait that is unique, enhanced or altered in a domesticated plant as compared to a wild ancestor of said domesticated plant, said method comprising contacting at least one candidate agent with the transgenic plant or transfected cell produced according to the method of claim 1, wherein the agent is identified by its ability to modulate the relevant trait.

7. The method of claim 6, wherein said identified agent modulates the relevant trait by modulating a function of the polynucleotide encoding the polypeptide.

8. The method of claim 6, wherein said identified agent modulates the relevant trait by modulating a function of the polypeptide.

9. A method of identifying sites in an evolutionarily significant polynucleotide in a domesticated plant wherein said polynucleotide's function can be modulated by an agent, comprising identifying those nucleotide changes in the polynucleotide that are evolutionarily significant in the domesticated plant, and contacting said agent with said polynucleotide whereby the function of the polynucleotide is modulated through direct or indirect interaction with said changes.

10. A method of identifying sites in an evolutionarily significant polypeptide in a domesticated plant wherein said polypeptide's function can be modulated by an agent, comprising identifying those amino acid changes in the polypeptide that are evolutionarily significant in the domesticated plant, and contacting said agent with said polypeptide whereby the function of the polypeptide is modulated through direct or indirect interaction with said changes.

11. The method of claim 1, wherein the domesticated plant is selected from the group consisting of corn, rice, tomato, potato, wheat, sorghum and millet.

12. The method of claim 1, wherein said relevant trait of said domesticated plant is selected from the group consisting of yield, short day length flowering, protein content, oil content, taste, ease of harvest, disease resistance and drought resistance.

13. The method of claim 5, wherein the polypeptide-coding nucleotide sequences of said domesticated plant correspond to cDNA.

14. The method of claim 5, wherein the nucleotide change is a non-synonymous substitution.

15. The method of claim 14, wherein the evolutionary significance of the nucleotide change is determined according to the non-synonymous substitution rate (K.sub.A) of the nucleotide sequence.

16. The method of claim 15, wherein the evolutionary significance of the nucleotide change is determined by the ratio of the non-synonymous substitution rate (K.sub.A) to the synonymous rate (K.sub.S) of the nucleotide sequence.

17. The method of claim 16, wherein the K.sub.A /K.sub.S ratio is at least about 0.00.

18. The method of claim 16, wherein the K.sub.A /K.sub.S ratio is at least about 1.25.

19. The method of claim 16, wherein the K.sub.A /K.sub.S ratio is at least about 1.50.

20. A method for large scale sequence comparison between polypeptide-coding nucleotide sequences of a domesticated plant and polypeptide-coding sequences from a wild ancestor of said domesticated plant, wherein said polypeptide is or is suspected or being associated with a commercially or aesthetically relevant trait that is unique, enhanced or altered in the domesticated plant as compared to a wild ancestor of said domesticated plant, said method comprising: a) aligning the domesticated plant sequences with corresponding sequences from the wild ancestor according to sequence homology; and b) identifying any nucleotide changes within the domesticated plant sequences as compared to the homologous sequences from the wild ancestor.

21. The method of claim 20, wherein the domesticated plant is selected from the group consisting of corn, rice, tomato, potato, wheat, sorghum and millet.

22. The method of claim 20, wherein the polypeptide-coding sequences of said domesticated plant corresponds to cDNA.

23. A method for correlating an evolutionarily significant nucleotide change with a commercially or aesthetically relevant trait that is unique, enhanced or altered in a domesticated plant, comprising: a) identifying a polynucleotide sequence encoding a polypeptide of a domesticated plant, wherein said polypeptide is or is suspected of being associated with a commercially or aesthetically relevant trait that is unique, enhanced or altered in the domesticated plant as compared to a wild ancestor of said domesticated plant; and b) analyzing the functional effect of the presence or absence of the identified sequence in the domesticated plant.

24. A method of making a transfected cell comprising: a) identifying an evolutionarily significant polynucleotide that encodes an evolutionarily significant polypeptide in a domesticated plant; b) identifying from said polynucleotide a non-polypeptide coding sequence that is a transcription or translation regulatory element, enhancer, intron or other 5' or 3' flanking sequence; c) assembling a construct comprising said non-polypeptide coding sequence and a polynucleotide encoding said evolutionarily significant polypeptide or a reporter protein; and d) transfecting said construct into a cell.

25. A method of making a transgenic plant comprising the method of claim 24, wherein said cell is a plant cell, whereby a transgenic plant is created from said transfected plant cell.

26. A method of identifying an agent that modulates the function of the non-polypeptide coding regions of an evolutionarily significant polynucleotide, comprising contacting the transfected cell of claim 24, with at least one candidate agent, wherein the agent is identified by its ability to modulate the transcription or translation of said evolutionarily significant polypeptide or said reporter polynucleotide.

27. A method of identifying an agent that modulates the function of a non-polypeptide coding region of an evolutionarily significant polynucleotide, comprising contacting the transgenic plant of claim 25 with at least one candidate agent, wherein the agent is identified by its ability to modulate the transcription or translation of said evolutionarily significant polypeptide or said reporter polynucleotide.

Details for Patent 6,743,580

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 ⤷  Try a Trial 2019-01-29
Merck Sharp & Dohme Corp. INTRON A interferon alfa-2b For Injection 103132 ⤷  Try a Trial 2019-01-29
Merck Sharp & Dohme Corp. INTRON A interferon alfa-2b Injection 103132 ⤷  Try a Trial 2019-01-29
>Applicant >Tradename >Biologic Ingredient >Dosage Form >BLA >Approval Date >Patent No. >Expiredate

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