DOMINANT-NEGATIVE GENETIC MANIPULATION TO MAKE LOW-NICOTINE TOBACCO PRODUCTS
The present technology provides dominant negative forms of transcription factors for modifying nicotine biosynthesis and nucleic acid molecules that encode such dominant negative transcription factors. Also provided are methods of using these nucleic acids to modulate nicotine production in plants and for producing plants and plant cells having reduced nicotine content.
1 . A chimeric nucleic acid construct comprising at least one transcription repressor sequence in translational fusion with at least one transcription factor sequence encoding for a transcription factor or fragment thereof that positively regulates nicotine biosynthesis, wherein the chimeric nucleic acid construct is operably linked to a heterologous nucleic acid.
2 . The chimeric nucleic acid of claim 1 , wherein the transcription repressor sequence encodes for a transcription repressor selected from the group consisting of: Engrailed (En 298 ) (SEQ ID NO: 11), SRDX (SEQ ID NO: 12), AtERF4 (SEQ ID NO: 13), NtERF3 (SEQ ID NO: 15), SUPERMAN (SEQ ID NO: 17), LEUNIG (SEQ ID NO: 18), and SEUSS (SEQ ID NO: 19).
3 . The chimeric nucleic acid of claim 1 , wherein the transcription factor sequence encoding for a transcription factor or fragment thereof that positively regulates nicotine biosynthesis is selected from the group consisting of:
(a) the nucleic acid sequence of SEQ ID NO: 1 (NtERF1), SEQ ID NO: 2 (NtERF5), SEQ ID NO: 3 (NtERF10), SEQ ID NO: 4 (NtERF32), SEQ ID NO: 5 (NtERF221), SEQ ID NO: 6 (NtERF241), SEQ ID NO: 7 (NtMYC1a), SEQ ID NO: 8 (NtMYC1b), SEQ ID NO: 9 (NtMYC2a), or SEQ ID NO: 10 (NtMYC2b); and
(b) a nucleic acid sequence that is at least about 80% identical to the nucleic acid sequence of (a), and which encodes for a protein comprising at least one DNA binding domain that positively regulates nicotine biosynthesis.
4 . An expression vector comprising the chimeric nucleic acid of claim 1 , wherein the operably linked heterologous nucleic acid comprises one or more control sequences suitable for directing expression in a Nicotiana host cell.
5 . A Nicotiana host cell transformed with the chimeric nucleic acid construct of claim 1 .
6 . A genetically engineered nicotinic alkaloid-producing Nicotiana plant comprising a cell comprising the chimeric nucleic acid construct of claim 1 .
7 . The engineered Nicotiana plant of claim 6 , wherein the plant is a Nicotiana tabacum plant.
8 . Seeds from the genetically engineered Nicotiana plant of claim 6 , wherein the seeds comprise the chimeric nucleic acid construct.
9 . A tobacco product comprising the engineered Nicotiana plant of claim 6 .
10 . A method for reducing nicotine in a Nicotiana plant, comprising:
(a) introducing into a Nicotiana plant an expression vector comprising a chimeric nucleic acid construct comprising, in the 5′ to 3′ direction, a promoter suitable for directing expression in a Nicotiana plant cell operably linked to at least one transcription repressor sequence in translational fusion with at least one transcription factor sequence encoding for a transcription factor or fragment thereof that positively regulates nicotine biosynthesis; and
(b) growing the plant under conditions which allow for the expression of the chimeric nucleic acid;
wherein expression of the chimeric nucleic acid results in production of a dominant negative form of the transcription factor and the plant having a reduced nicotine content as compared to a non-transformed control plant grown under similar conditions.
11 . The method of claim 10 , wherein the transcription repressor sequence encodes for transcription repressor selected from the group consisting of: Engrailed (En 298 ) (SEQ ID NO: 11), SRDX (SEQ ID NO: 12), AtERF4 (SEQ ID NO: 13), NtERF3 (SEQ ID NO: 15), SUPERMAN (SEQ ID NO: 17), LEUNIG (SEQ ID NO: 18), and SEUSS (SEQ ID NO: 19).
12 . The method of claim 10 , wherein the transcription factor that positively regulates nicotine biosynthesis is selected from the group consisting of:
(a) the nucleic acid sequence of SEQ ID NO: 1 (NtERF1), SEQ ID NO: 2 (NtERF5), SEQ ID NO: 3 (NtERF10), SEQ ID NO: 4 (NtERF32), SEQ ID NO: 5 (NtERF221), SEQ ID NO: 6 (NtERF241), SEQ ID NO: 7 (NtMYC1a), SEQ ID NO: 8 (NtMYC1b), SEQ ID NO: 9 (NtMYC2a), or SEQ ID NO: 10 (NtMYC2b); and
(b) a nucleic acid sequence that is at least 80% identical to the nucleic acid sequence of (a), and which encodes for a protein comprising at least one DNA binding domain that positively regulates nicotine biosynthesis.
13 . A genetically engineered Nicotiana plant produced by the method of claim 10 , wherein the plant has reduced expression of nicotine as compared to a control plant.
14 . A product comprising the genetically engineered plant of claim 13 or portions thereof, wherein the product has a reduced nicotine content as compared to a product produced from a control plant.
15 . The product of claim 14 , wherein the product is a reduced-nicotine tobacco product selected from the group consisting of cigarette tobacco, reconstituted tobacco, cigar tobacco, pipe tobacco, cigarettes, cigars, chewing tobacco, snuff, snus, and lozenges.
16 . Seeds from the genetically engineered Nicotiana plant of claim 13 , wherein the seeds comprise the chimeric nucleic acid construct.
17 . A genetically engineered Nicotiana plant having reduced nicotine content as compared to a non-transformed control plant, wherein the plant comprises plant cells comprising:
a chimeric nucleic acid construct comprising, in the 5′ to 3′ direction, a promoter suitable for directing expression in the Nicotiana plant cell operably linked to at least one transcription repressor sequence in translational fusion with at least one transcription factor sequence encoding for a transcription factor or fragment thereof that positively regulates nicotine biosynthesis,
wherein expression of the chimeric nucleic acid results in production of a dominant negative form of the transcription factor and the plant having a reduced nicotine content as compared to a non-transformed control plant grown under similar conditions.
18 . The plant of claim 17 , wherein the transcription repressor sequence encodes for a transcription repressor selected from the group consisting of: Engrailed (En 298 ) (SEQ ID NO: 11), SRDX (SEQ ID NO: 12), AtERF4 (SEQ ID NO: 13), NtERF3 (SEQ ID NO: 15), SUPERMAN (SEQ ID NO: 17), LEUNIG (SEQ ID NO: 18), and SEUSS (SEQ ID NO: 19).
19 . The plant of claim 17 , wherein the transcription factor that positively regulates nicotine biosynthesis is selected from the group consisting of:
(a) the nucleic acid sequence of SEQ ID NO: 1 (NtERF1), SEQ ID NO: 2 (NtERF5), SEQ ID NO: 3 (NtERF10), SEQ ID NO: 4 (NtERF32), SEQ ID NO: 5 (NtERF221), SEQ ID NO: 6 (NtERF241), SEQ ID NO: 7 (NtMYC1a), SEQ ID NO: 8 (NtMYC1b), SEQ ID NO: 9 (NtMYC2a), or SEQ ID NO: 10 (NtMYC2b); and
(b) a nucleic acid sequence that is at least about 80% identical to the nucleic acid sequence of (a), and which encodes for a protein comprising at least one DNA binding domain that positively regulates nicotine biosynthesis.
20 . A product comprising the genetically engineered plant of claim 17 or portions thereof, wherein the product has a reduced nicotine content as compared to a product produced from a control plant.
21 . The product of claim 20 , wherein the product is a reduced-nicotine tobacco product selected from the group consisting of cigarette tobacco, reconstituted tobacco, cigar tobacco, pipe tobacco, cigarettes, cigars, chewing tobacco, snuff, snus, and lozenges.
22 . Seeds from the genetically engineered Nicotiana plant of claim 17 , wherein the seeds comprise the chimeric nucleic acid construct.
23 . A method of making a genetically engineered Nicotiana plant cell having reduced nicotine content, the method comprising:
introducing into a Nicotiana plant cell an expression vector comprising a chimeric nucleic acid construct comprising, in the 5′ to 3′ direction, a promoter suitable for directing expression in a Nicotiana plant cell operably linked to at least one transcription repressor sequence in translational fusion with at least one transcription factor sequence encoding for a transcription factor or fragment thereof that positively regulates nicotine biosynthesis;
wherein expression of the chimeric nucleic acid results in production of a dominant negative form of the transcription factor and the plant cell having a reduced nicotine content as compared to a non-transformed control plant cell.
24 . The method of claim 23 , wherein the transcription repressor sequence encodes for transcription repressor selected from the group consisting of: Engrailed (En 298 ) (SEQ ID NO: 11), SRDX (SEQ ID NO: 12), AtERF4 (SEQ ID NO: 13), NtERF3 (SEQ ID NO: 15), SUPERMAN (SEQ ID NO: 17), LEUNIG (SEQ ID NO: 18), and SEUSS (SEQ ID NO: 19).
25 . The method of claim 23 , wherein the transcription factor that positively regulates nicotine biosynthesis is selected from the group comprising of:
(a) the nucleic acid sequence of SEQ ID NO: 1 (NtERF1), SEQ ID NO: 2 (NtERF5), SEQ ID NO: 3 (NtERF10), SEQ ID NO: 4 (NtERF32), SEQ ID NO: 5 (NtERF221), SEQ ID NO: 6 (NtERF241), SEQ ID NO: 7 (NtMYC1a), SEQ ID NO: 8 (NtMYC1b), SEQ ID NO: 9 (NtMYC2a), or SEQ ID NO: 10 (NtMYC2b); and
(b) a nucleic acid sequence that is at least about 80% identical to the nucleic acid sequence of (a), and which encodes for a protein comprising at least one DNA binding domain that positively regulates nicotine biosynthesis.
26 . The method of claim 23 , wherein the Nicotiana plant cell is Nicotiana tabacum.