Methods and compositions for targeted integration in a plant

Patent metadata

Field	Value
Publication number	US-9951346-B2
Application number	US-201214236597-A
Country	US
Kind code	B2
Filing date	Jul 18, 2012
Priority date	Aug 3, 2011
Publication date	Apr 24, 2018
Grant date	Apr 24, 2018

Abstract

Compositions and methods are provided for the targeted integration of a polynucleotide sequence of interest into the genome of a plant or plant cell. The methods and compositions employ recognition sites for endonucleases and endonucleases in combination with site-specific recombination sites/recombinases to provide an effective system for establishing target sites within the genome of a plant, plant cell or seed. Once such target sites are established, a variety of methods can be employed to further modify the target sites such that they contain a variety of polynucleotides of interest.

First claim

That which is claimed:

1. A method for introducing into the genome of a plant cell a target site for site-specific integration, the method comprising:
(a) providing a plant cell comprising in its genome an endogenous recognition site for an engineered meganuclease, wherein the endogenous recognition site is located between a first and a second genomic region, and wherein the endogenous recognition site is selected from the group consisting of SEQ ID NO: 1, 2, 3, 4, 5, 6, 7, and 8;
(b) providing a donor DNA comprising the target site for site-specific integration located between a first region of homology to said first genomic region and a second region of homology to said second genomic region, wherein the target site comprises a first and a second recombination site, and wherein the first and the second recombination sites are dissimilar and non-recombinogenic with respect to one another;
(c) contacting the plant cell with the donor DNA and the engineered meganuclease, wherein the engineered meganuclease induces a double-strand break in said endogenous recognition site; and
(d) identifying at least one plant cell from (c) comprising in its genome the target site integrated at the endogenous recognition site.

2. The method of claim 1 , wherein the first region of homology further comprises a first fragment of said endogenous recognition site of (a), and wherein the second region of homology comprises a second fragment of said endogenous recognition site of (a), wherein the first and second fragments are dissimilar.

3. The method of claim 1 , wherein the first region of homology further comprises the first 13 bases of said endogenous recognition site of (a), and wherein the second region of homology comprises the last 9 bases of said endogenous recognition site of (a).

4. The method of claim 1 , further comprising recovering a fertile plant from the cell of (d), the fertile plant comprising in its genome the target site integrated into the endogenous recognition site.

5. The method of claim 1 , wherein the target site further comprises a polynucleotide of interest between the first recombination site and the second recombination site.

6. The method of claim 1 , wherein at least one of the recombination sites comprises a site selected from the group consisting of an FRT site, a mutant FRT site, a LOX site, and a mutant LOX site.

7. The method of claim 1 , wherein the target site further comprises a third recombination site between the first and the second recombination site, wherein the third recombination site is dissimilar and non-recombinogenic to the first and the second recombination sites.

8. The method of claim 7 , wherein at least one of the recombination sites comprises a site selected from the group consisting of FRT1 (SEQ ID NO: 9), FRT 5(SEQ ID NO: 10), FRT6 (SEQ ID NO: 11), FRT12 (SEQ ID NO: 12) and FRT87 (SEQ ID NO:13).

9. The method of claim 7 , wherein the first recombination site is FRT1 (SEQ ID NO: 9), the second recombination site is FRT12 (SEQ ID NO: 12), and the third recombination site is FRT87 (SEQ ID NO: 13).

10. The method of claim 1 , wherein the engineered meganuclease is derived from I-CreI.

11. The method of claim 1 , wherein said plant cell is from a dicot.

12. The method of claim 11 , wherein said dicot is soybean.

13. A method of integrating a polynucleotide of interest into a target site in the genome of a plant cell, the method comprising:
(a) providing at least one plant cell comprising in its genome a target site for site-specific integration, wherein the target site is integrated into an endogenous recognition site for an engineered meganuclease, wherein the endogenous recognition site is selected from the group consisting of SEQ ID NO: 1, 2, 3, 4, 5, 6, 7, and 8, and wherein the target site is,
(i) a target site comprising a first and a second recombination site; or
(ii) the target site of (i) further comprising a third recombination site between the first recombination site and the second recombination site,

wherein the engineered meganuclease induces a double-strand break in the endogenous recognition site, wherein the first, the second, and the third recombination sites are dissimilar and non-recombinogenic with respect to one another,
(b) introducing into the plant cell of (a) a transfer cassette comprising,
(iii) the first recombination site, a first polynucleotide of interest, and the second recombination site,
(iv) the second recombination site, a second polynucleotide of interest, and the third recombination sites, or
(v) the first recombination site, a third polynucleotide of interest, and the third recombination sites;

(c) providing a recombinase that recognizes and implements recombination at the first and the second recombination sites, at the second and the third recombination sites, or at the first and third recombination sites; and
(d) selecting at least one plant cell comprising integration of the transfer cassette at the target site.

14. The method of claim 13 , further comprising recovering a fertile plant from the plant cell of (d), the fertile plant comprising in its genome the transfer cassette at the target site.

15. The method of claim 13 , wherein at least one of the first, the second, and the third polynucleotides of interest comprises a nucleotide sequence for gene silencing, a nucleotide sequence encoding a phenotypic marker, or a nucleotide sequence encoding a protein providing an agronomic advantage.

16. The method of claim 13 , wherein providing the recombinase comprises integrating into the genome of the plant cell a nucleotide sequence encoding the recombinase.

17. The method of claim 13 , wherein the transfer cassette further comprises at least one coding region operably linked to a promoter that drives expression in the plant cell.

18. The method of claim 13 , wherein the transfer cassette further comprises a coding region operably linked to a promoter that drives expression in the plant cell, wherein the coding region encodes a recombinase that facilitates recombination between, the first and the second recombination sites of the transfer cassette and the target site, the second and the third recombination sites of the transfer cassette and the target site, or the first and the third recombination sites of the transfer cassette and the target site.

19. The method of claim 13 , wherein at least one of the recombination sites comprises a site selected from the group consisting of an FRT site, a mutant FRT site, a LOX site, and a mutant LOX site.

20. The method of claim 13 , wherein the first recombination site is FRT1 (SEQ ID NO: 9), the second recombination site is FRT12 (SEQ ID NO: 12), and the third recombination site is FRT87 (SEQ ID NO: 13).

21. The method of claim 13 , wherein the recombinase is FLP.

22. The method of claim 21 , wherein the FLP has been synthesized using maize-preferred codons.

23. The method of claim 13 , wherein said plant cell is from a dicot.

24. The method of claim 23 , wherein said dicot is soybean.

25. A plant cell, plant part, plant, or seed comprising the transfer cassette integrated at the target site according to the method of claim 13 .

26. A plant, seed or plant cell comprising in its genome a target site for site-specific integration, wherein the target site is integrated into an endogenous recognition site for an engineered meganuclease, wherein the endogenous recognition site i

Assignees

• Cigan Andrew Mark
• Falco Saverio Carl
• Gao Huirong
• Lassner Michael W
• Li Zhongsen
• Liu Zhan Bin
• Lyznik Leszek A
• Peterson David J
• Scelonge Christopher Jay
• Pioneer Hi Bred Int
• Du Pont

Inventors

• Cigan Andrew Mark
• Falco Saverio Carl
• Gao Huirong
• Lassner Michael W
• Li Zhongsen
• Liu Zhan-Bin
• Lyznik Leszek A
• Peterson David J
• Scelonge Christopher Jay

Classifications

• C12N15/8213 Primary

  Targeted insertion of genes into the plant genome by homologous recombination · CPC title