Excision of transgenes in genetically modified organisms

Patent metadata

Field	Value
Publication number	US-9695432-B2
Application number	US-201113011666-A
Country	US
Kind code	B2
Filing date	Jan 21, 2011
Priority date	Jan 22, 2010
Publication date	Jul 4, 2017
Grant date	Jul 4, 2017

Abstract

A method for deleting a region of DNA in a plant. In some embodiments, the method comprises transforming a plant with a nucleic acid molecule, wherein the nucleic acid molecule encodes one or more zinc finger nuclease(s) (ZFNs) operably linked to one or more tissue-specific promoter(s), e.g., a pollen-specific promoter. Methods include excising native genes in a plant. Accordingly, in some embodiments, ZFNs are engineered that recognize sequences that flank native plant genes. In further embodiments, ZFNs are expressed under the control of developmental stage-specific promoters, such that, for example, nucleic acid sequences are specifically excised in plants during relatively late stages of development. Nucleic acid molecules useful for carrying out disclosed methods and plants produced by the methods are included.

First claim

What is claimed is:

1. An isolated nucleic acid molecule comprising:
a promoter; and
a nucleic acid sequence encoding a zinc finger nuclease, wherein the promoter is operably linked to the nucleic acid sequence encoding the zinc finger nuclease, wherein the nucleic acid sequence is flanked by zinc finger nuclease cleavage sites.

2. A method of producing a transgenic plant comprising:
transforming a plant cell or plant tissue with the isolated nucleic acid molecule of claim 1 ; and
regenerating a whole plant.

3. The isolated nucleic acid molecule of claim 1 , wherein the promoter is selected from the group consisting of: a pollen-specific promoter, a seed-specific promoter, and a developmental-stage specific promoter.

4. A method for deleting a polynucleotide in a plant, the method comprising:
crossing a first viable plant and a second viable plant such that F1 seed is produced on either the first or the second viable plant;
wherein the first viable plant is a plant produced by the method according to claim 2 ; and
wherein the second viable plant comprises genomic DNA comprising, in the 5′ to 3′ direct: a first cleavage site for the zinc finger nuclease, the polynucleotide, and a second cleavage site for the zinc finger nuclease; and

growing a resultant transgenic F1 plant, wherein the polynucleotide is absent from the genomic DNA.

5. The method of claim 4 , wherein the first cleavage site for the zinc finger nuclease and the second cleavage site for the zinc finger nuclease are identical.

6. The transgenic plant produced by the method of claim 4 .

7. A method for deleting a region of DNA in a plant cell, the method comprising:
providing a nucleic acid comprising a first polynucleotide which is recognized and cleaved by a zinc finger nuclease, a selectable marker gene expression cassette, and a second polynucleotide which is recognized and cleaved by a zinc finger nuclease, wherein the selectable marker is flanked by the first and second polynucleotides,
wherein the nucleic acid of claim 1 is introduced into the plant cell and either the first or the second polynucleotide is recognized and cleaved by the zinc finger nuclease encoded by the nucleic acid of claim 1 , so as to cleave the DNA at either the first or the second polynucleotide,
thereby resulting in the excision of the selectable marker from the DNA.

8. The method of claim 7 , wherein the first polynucleotide and the second polynucleotide are flanked by polynucleotides capable of homologous recombination with each other.

9. The method of claim 7 , further comprising introducing into the plant cell a zing finger nuclease that recognizes and cleaves either the first or the second polynucleotide.

10. The method according to claim 7 , wherein the first and second polynucleotides are the same.

11. The method according to claim 4 , wherein the first and second cleavage sites for the zinc finger nuclease are flanked by polynucleotides capable of homologous recombination with each other.

12. A method of excising a native gene of interest in a plant comprising:
transforming a plant cell or tissue comprising a gene of interest with an isolated nucleic acid molecule encoding a zinc finger nuclease, wherein the zinc finger nuclease recognizes and cleaves at a first polynucleotide positioned 5′ with respect to the native gene of interest; and
wherein the zinc finger nuclease recognizes and cleaves at a second polynucleotide positioned 3′ with respect to the native gene of interest; and
regenerating a whole plant.

13. The method according to claim 12 , wherein the first and second polynucleotides recognized and cleaved by the zinc finger nuclease are flanked by polynucleotides capable of homologous recombination with each other.

Assignees

• Russell Sean M
• Petolino Joseph F
• Dow Agrosciences Llc

Inventors

• Russell Sean M
• Petolino Joseph F

Classifications

• C12N9/22

  Ribonucleases {[RNase]; Deoxyribonucleases [DNase]} · CPC title

• C12N15/8265

  Transgene containment, e.g. gene dispersal · CPC title

• C12N15/8213 Primary

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

• C12N15/8241 Primary

  Phenotypically and genetically modified plants via recombinant DNA technology · CPC title

• A01H1/02

  Methods or apparatus for hybridisation; Artificial pollination {; Fertility} · CPC title