Methods and Compositions for Improving the Efficiency of Site-Specific Polynucleotide Exchange

Abstract

Methods and compositions using a site-specific integration system are combined with methods and compositions which deliver compositions via microinjection directly to the embryo sac of a plant. The methods allow for various components of the site-specific recombination system to be introduced into the cellular environment of the embryo sac a composition comprising at least one component of the site-specific recombination system is injected into an embryo sac, providing improved efficiency of expression, recombination, integration, exchange, excision and/or inversion of a polynucleotide of interest. The polynucleotide of interest may be stably integrated into the genome of the egg cell, zygote, embryo, or endosperm, and tissues, plant parts, and/or plants produced therefrom. Cells, egg cells, zygotes, embryos, endosperm, tissues, seeds, and/or plants produced by the methods and comprising the polynucleotide(s) of interest are also provided.

Description

BRIEF DESCRIPTION OF DRAWINGS

FIG. 1 shows an embryo/endosperm structure derived from a 1-day post-pollinated microinjected nucellar slab after 21 days in vitro culture. The nucellar slab, isolated from a transgenic plant stably transformed with PHP10006 (Ubi::FRT1::GFP::35S::MOPAT::FRT1::GUS::FRT5), was injected with Agrobacterium containing PHP17797 (RB::Ubi-FRT1::FLPm::35S::Bar::FRT5::LB). The FLP enzyme expressed from PHP17797 mediated excision of the DNA between the FRT1 sites in PHP10006 in the injected slab, thereby creating an operable linkage of the promoterless GUS gene to the Ubi promoter, resulting in GUS expression. The blue spot (arrow) shows the GUS expression in the embryo area, demonstrating T-DNA transfer and gene expression from the injected Agrobacterium. Bar=1 mm.

Claims

1. A method for targeting a polynucleotide of interest to a target site in a plant comprising a) providing an embryo sac from the plant, wherein the embryo sac comprises a target site stably incorporated into its genome, the target site comprising a first recombination site;b) injecting into the embryo sac an effective concentration of an Agrobacterium comprising a T-DNA, wherein the T-DNA comprises the first recombination site and the polynucleotide of interest, wherein the Agrobacterium is capable of T-DNA transfer into a plant cell; and,c) providing a recombinase, wherein the recombinase recognizes and implements recombination at the first recombination site,whereby the polynucleotide of interest is inserted at the target site.

2. The method of claim 1 wherein the embryo sac of step (a) has stably incorporated into its genome the target site, wherein the target site comprises the first recombination site and a second recombination site, wherein the first and the second recombination sites are dissimilar and non-recombinogenic with respect to one another; and,the T-DNA comprises a transfer cassette, the transfer cassette comprising in the following order, the first recombination site, the polynucleotide of interest, and the second recombination site; and,wherein the recombinase recognizes and implements recombination at the first and the second recombination sites, whereby the polynucleotide of interest is inserted at the target site.

3. The method of claim 2, wherein the transfer cassette comprises in the following order, the first recombination site, a promoter operably linked to the polynucleotide of interest, and the second recombination site.

4. The method of claim 2 wherein the embryo sac of step (a) has stably incorporated into its genome a polynucleotide comprising in the following order, a promoter operably linked to the target site,the transfer cassette comprises in the following order, the first recombination site, the polynucleotide of interest, and the second recombination site, wherein the polynucleotide of interest is not operably linked to a promoter.

5. The method of claim 1, further comprising recovering a targeted plant from the embryo sac, wherein the targeted plant has the polynucleotide of interest stably incorporated into its genome at the target site.

6. The method of claim 2, further comprising recovering a targeted plant from the embryo sac, wherein the targeted plant has the polynucleotide of interest stably incorporated into its genome at the target site.

7. The method of claim 2, wherein the embryo sac of step (a) has stably incorporated into its genome a polynucleotide comprising in the following order, a promoter active in the plant operably linked to an ATG translational start site operably linked to the target site,the transfer cassette comprising, in the following order, the first recombination site, the polynucleotide of interest, and the second recombination site, wherein the ATG translation start of the polynucleotide of interest has been replaced with the first recombination site, whereby recombination with the target site results in the polynucleotide of interest being operably linked to the ATG translational start site.

8. The method of claim 1, wherein the providing the recombinase comprises providing a polynucleotide encoding the recombinase, wherein the polynucleotide can be stably integrated in the genome of the plant or the T-DNA.

9. The method of claim 1, wherein the recombinase is a FLP recombinase or a Cre recombinase.

10. The method of claim 8 wherein the recombinase is encoded by a polynucleotide having maize preferred codons.

11. The method of claim 2, wherein the transfer cassette comprises in the following order, the first recombination site, a polynucleotide of interest, a third recombination site, and the second recombination site, wherein the first, the second, and the third recombination sites are dissimilar and non-recombinogenic with respect to one another.

12. The method of claim 2, wherein the target site comprises in the following order, the first recombination site, the polynucleotide of interest, the second recombination site, and a third recombination site; wherein the first, the second, and the third recombination sites are dissimilar and non-recombinogenic with respect to one another;the transfer cassette comprises in the following order, the second recombination site, a second polynucleotide of interest, and the third recombination site; and,providing the recombinase, wherein the recombinase recognizes and implements recombination at the recombination sites of the transfer cassette, whereby the second polynucleotide of interest is inserted at the target site.

13. The method of claim 2, wherein at least one of the dissimilar and non-recombinogenic recombination sites is selected from the group consisting of a FRT site, and a LOX site.

14. The method of claim 1, wherein the first recombination site is selected from the group consisting of a FRT site, and a LOX site.

15. The method of claim 1, wherein the embryo sac comprises a fertilized embryo sac.

16. The method of claim 15, wherein the fertilized embryo sac comprises an embryo or a zygote.

17. The method of claim 1 wherein the plant is a monocot or a dicot.

18. A method of introducing into a plant a recombinase polypeptide comprising injecting into an embryo sac of the plant a composition comprising an Agrobacterium comprising a T-DNA comprising a promoter active in the embryo sac operably linked to a polynucleotide encoding the recombinase, wherein the Agrobacterium is capable of T-DNA transfer into a plant cell.

19. A method for locating preferred integration sites within the genome of a plant comprising a) injecting into an embryo sac from the plant a composition comprising an effective concentration of an Agrobacterium comprising a T-DNA comprising a first recombination site and a polynucleotide of interest, wherein the Agrobacterium is capable of T-DNA transfer into a plant cell;b) monitoring the level of expression of the polynucleotide of interest; and,c) selecting the embryo sac or the plant recovered therefrom expressing the polynucleotide of interest.

20. The method of claim 19 wherein the T-DNA comprises a target site comprising in the following order, the first recombination site, the polynucleotide of interest, and a second recombination site, wherein the first and the second recombination sites are dissimilar and non-recombinogenic with respect to one another.