Methods and vectors for site-specific recombination in plant cell plastids
Novel compositions and methods useful for genetic engineering of plant cells are provided. In particular, plastid constructs comprising recombining sites are provided. Such constructs find use in methods for site specific recombination in plant cell plastids. Plant cells and plants comprising the constructs described herein, as well as plant cells and plants produced by the methods of the present invention are of interest.
1. A method for performing multiple rounds of plastid transformations in a plant cell plastid using the same selectable marker for selection of transplastomic plants comprising:
(a) introducing into a plant cell a first recombinant DNA sequence comprising a construct capable of being integrated into the plastid genome of the plant cell, said construct comprising an expression cassette comprising a DNA sequence of interest to be expressed in the plastid and a selectable marker cassette comprising a promoter that initiates expression of an operably linked DNA sequence in a plant plastid, a DNA sequence encoding a protein that permits for the selection of a transformed plastid and a 3′ transcription termination region, said selectable marker cassette flanked by a pair of compatible recombining sites arranged in parallel orientation as direct repeats, to produce a plant cell having a plastid containing said first recombinant DNA sequence;
(b) selecting for the cell containing a transformed plastid;
(c) providing a recombinase compatible to said pair of compatible recombining sites to said plant cell to permit excision of said DNA sequence encoding a protein that permits for the selection of a transformed plastid and producing excision of said DNA sequence;
(d) regenerating a transplastomic plant containing said first recombinant DNA sequence without said DNA sequence encoding a protein that permits for the selection of a transformed plastid from said plant cell;
(e) introducing into a plant cell of said transplastomic plant a second recombinant DNA sequence comprising a construct capable of being integrated into the plastid genome of the plant cell, said construct comprising a second expression cassette comprising a second DNA sequence of interest to be expressed in said plastid and a second selectable marker cassette comprising a promoter that initiates expression of an operably linked DNA sequence in a plant plastid, a DNA sequence encoding the same protein as in the first recombinant DNA sequence that permits for the selection of a transformed plastid and a 3′ transcription termination region, into a plant cell of said transplastomic plant obtained from said regenerated plant thereby producing a plastid having said second recombinant DNA sequence in said plant cell of said transplastomic plant; and
(f) producing a transplastomic plant having said first and second recombinant DNA sequences introduced sequentially into said plastid using the same selectable marker for the second recombinant DNA sequence as used for the selection of the first recombinant DNA sequence.
2. The method according to claim 1 , wherein said recombinase is provided to said plant cell by introducing a third recombinant DNA sequence comprising in an operably coupled 5′ to 3′ manner:
a transcriptional initiation region, a plastid targeting region, and a nucleic acid sequence encoding recombinase.
3. The method according to claim 1 , wherein said DNA sequence of interest in said first or second expression cassette provides for herbicide resistance to said plant cell.
4. The method according to claim 1 , wherein said pair of compatible recombining sites is selected from the group consisting of Lox, FRT and R.