Nuclear-encoded transcription system in plastids of higher plants
AssigneeRutgers, The State University of New Jersey
InventorsPal Maliga, Lori A. Allison, Peter T. Hajdukiewicz
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Abstract
The present invention provides novel DNA constructs and methods for stably transforming the plastids of higher plants. The constructs described herein contain unique promoters that are transcribed by both nuclear encoded plastid polymerases and plastid encoded plastid polymerases. Use of the novel constructs of the invention facilitates transformation of a wider range of plant species and enables tissue specific expression of a transforming DNA in plastids of multicellular plants.
Claims9
A DNA construct for stably transforming plastids of multicellular plants, wherein the construct comprises:
- a transforming DNA having a targeting segment which effects insertion of said transforming DNA into a plastid genome by homologous recombination without disrupting expression of essential genes,
- a selectable marker gene conferring a selectable phenotype to plant cells containing transformed plastids,
- a 3′ regulatory region located downstream of said selectable marker gene, wherein the region stabilizes mRNA, and
- a cloning site for insertion of an additional expressible DNA encoding a foreign protein of interest,
- wherein the improvement comprises a 5′ promoter element operably linked to said selectable marker gene wherein the promoter element is recognized and transcribed by a plant nuclear encoded plastid RNA polymerase, and wherein the promoter element is selected from the group consisting of Prrn-62 (SEQ ID NO:59), PORF2280-1577 (SEQ ID NO:60), PatpB-289 (SEQ ID NO:61), PORF1901-41 (SEQ ID NO:64), Prbs2-152 (SEQ ID NO:62), Prps16-107 (SEQ ID NO:63), PatpI-207 (SEQ ID NO:65), PclpP-511 (SEQ ID NO:66), PclpP-173 (SEQ ID NO:67), PclpP-53 (SEQ ID NO:70) and PaccD-129 (SEQ ID NO:68).
A DNA construct for stably transforming the plastids of a plant cell and for expression of at least one additional gene product therein, wherein the construct comprises:
- a) a targeting segment comprising a DNA sequence homologous to a plastid genomic sequence within a plastid to be transformed, said targeting segment enabling homologous recombination with said plastid genomic sequence without disrupting expression of essential genes;
- and
- b) a selectable marker gene disposed within said targeting segment and being operably linked to a first promoter sequence, said selectable marker gene conferring a selectable phenotype to cells containing plastids expressing said DNA construct;
- and
- c) an additional DNA segment comprising a transcription unit encoding a protein or a precursor thereof;
- d) a second promoter sequence which is operably linked to said transcription unit, wherein said second promoter sequence is recognized and transcribed by a plant nuclear encoded polymerase, said gene encoding said protein being regulated by said second promoter sequence, and
- e) at least one 3′ regulatory region which functions in plastids to stabilize mRNA transcribed from said DNA construct,
- wherein said second promoter sequence is selected from the group consisting of Prrn-62 (SEQ ID NO:59), PORF2280-1577 (SEQ ID NO:60), PatpB-289 (SEQ ID NO:61), PORF1901-41 (SEQ ID NO:64), Prps16-107 (SEQ ID NO:63), Prbs2-152 (SEQ ID NO:62), Patpl-207 (SEQ ID NO:65), PclpP-511 (SEQ ID NO:66), PclpP-173 (SEQ ID NO:67), PclpP-53 (SEQ ID NO:70) and PaccD-129 (SEQ ID NO:68).
A method for obtaining a multicellular plant, the plastids of which have been stably transformed by at least one foreign gene of interest, comprising
- administering to a plant cell a DNA construct comprising:
- a) a targeting segment comprising a DNA sequence homologous to a plastid genomic sequence within a plastid to be transformed, said targeting segment enabling homologous recombination with said plastid genomic sequence without disrupting expression of essential genes;
- and
- b) a selectable marker gene disposed within said targeting segment, wherein said selectable marker gene confers a selectable phenotype to cells containing plastids expressing said DNA construct, and wherein said selectable marker gene is operably linked to a promoter and further comprises a 3′ regulatory region for stabilizing mRNA;
- and
- c) a foreign gene of interest, wherein said foreign gene is regulated by a promoter selected from the group consisting of Prrn-62 (SEQ ID NO:59), PORF2280-1577 (SEQ ID NO:60), PatpB-289 (SEQ ID NO:61), PORF1901-41 (SEQ ID NO:64), Prbs2-152 (SEQ ID NO:62), Prps16-107 (SEQ ID NO:63), PatpI-207 (SEQ ID NO:65), PclpP-511 (SEQ ID NO:66), PclpP-173 (SEQ ID NO:67), PclpP-53 (SEQ ID NO:70) and PaccD-129 (SEQ ID NO:68);
- selecting for cells which express said selectable phenotype;
- and
- regenerating a plant from said cells.
Dependencies are inferred from the claim text.