US2008295202A1PendingUtilityA1
Soybean promoters SC194 and flower-preferred expression thereof in transgenic plants
Est. expiryMay 17, 2027(~0.8 yrs left)· nominal 20-yr term from priority
Inventors:Zhongsen Li
C12N 15/8222C12N 15/823
59
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Claims
Abstract
The promoters of a soybean SC194 polypeptide and fragments thereof and their use in promoting the expression of one or more heterologous nucleic acid fragments in plants are described.
Claims
exact text as granted — not AI-modified1 . An isolated polynucleotide comprising:
a) a nucleotide sequence comprising the sequence set forth in SEQ ID NO:1 or a full-length complement thereof; or b) a nucleotide sequence comprising a sequence having at least 90% sequence identity, based on the BLASTN method of alignment, when compared to the sequence set forth in SEQ ID NO:1;
wherein said nucleotide sequence is a promoter.
2 . The isolated polynucleotide of claim 1 , wherein the nucleotide sequence of b) has at 95% identity, based on the BLASTN method of alignment, when compared to the sequence set forth in SEQ ID NO:1.
3 . A recombinant DNA construct comprising the isolated polynucleotide of claim 1 operably linked to at least one heterologous sequence.
4 . The recombinant DNA construct of claim 3 , wherein the heterologous nucleotide sequence encodes a gene involved in anthocyanin biosynthesis, a gene involved in the synthesis of fragrant fatty acid derivatives, a gene that is determinative of flower morphology, or a gene involved in biosynthesis of plant cytokinin.
5 . The recombinant DNA construct of claim 4 , wherein the gene involved in anthocyanin biosynthesis is dyhydroflavonol 4-reductase, flavonoid 3,5-hydroxylase, chalcone synthase, chalcone isomerase, flavonoid 3-hydroxylase, anthocyanin synthase, or UDP-glucose 3-O-flavonoid glucosyl transferase.
6 . The recombinant DNA construct of claim 4 , wherein the gene involved in the synthesis of fragrant fatty acid derivatives is S-linalool synthase, acetyl CoA:benzylalcohol acetyltransferase, benzyl CoA:benzylalcohol benzoyl transferase, S-adenosyl-L-methionine:benzoic acid carboxylmethyl transferase, mycrene synthase, (E)-β-ocimene synthase, orcinol O-methyltransferase, or limonene synthase.
7 . The recombinant DNA construct of claim 4 , wherein the gene that is determinative of flower morphology is AGAMOUS, APETALA, or PISTILLATA.
8 . The recombinant DNA construct of claim 4 , wherein the gene involved in biosynthesis of plant cytokinin is isopentenyl transferase.
9 . A vector comprising the recombinant DNA construct of claim 3 .
10 . A cell comprising the recombinant DNA construct of claim 3 .
11 . The cell of claim 10 , wherein the cell is a plant cell.
12 . A transgenic plant having stably incorporated into its genome the recombinant DNA construct of claim 3 .
13 . The transgenic plant of claim 12 , wherein the plant is a flowering plant.
14 . The transgenic plant of claim 13 , wherein the flowering plant is rose, carnation, Gerbera, Chrysanthemum, tulip, Gladioli, Alstroemeria, Anthurium, Iisianthus, larkspur, irises, orchid, snapdragon, African violet, or azalea.
15 . A transgenic seed produced by the transgenic plant of claim 12 .
16 . A method of expressing a coding sequence or a functional RNA in a flowering plant comprising:
a) introducing the recombinant DNA construct of claim 3 into the plant, wherein the at least one heterologous sequence comprises a coding sequence or a functional RNA; b) growing the plant of step a); and c) selecting a plant displaying expression of the coding sequence or the functional RNA of the recombinant DNA construct.
17 . A method of transgenically altering a marketable flower trait of a flowering plant, comprising:
a) introducing a recombinant DNA construct of claim 3 into the flowering plant; b) growing a fertile, mature flowering plant resulting from step a); and c) selecting a flowering plant expressing the at least one heterologous nucleotide sequence in flower tissue based on the altered marketable flower trait.
18 . The method of claim 17 wherein the marketable flower trait is color, morphology, or fragrance.
19 . An isolated polynucleotide comprising:
(a) a nucleotide sequence comprising a fragment of SEQ ID NO:1, SEQ ID NO:2, SEQ ID NO:3, SEQ ID NO:4, SEQ ID NO:5, SEQ ID NO:6, or SEQ ID NO:7, or a full-length complement thereof; or (b) a nucleotide sequence comprising a sequence having at least 90% sequence identity, based on the BLASTN method of alignment, when compared to the nucleotide sequence of (a);
wherein said nucleotide sequence is a promoter.
20 . The isolated polynucleotide of claim 19 , wherein the nucleotide sequence of (a) comprises SEQ ID NO:2, SEQ ID NO:3, SEQ ID NO:4, SEQ ID NO:5, SEQ ID NO:6, or SEQ ID NO:7.
21 . An isolated polynucleotide comprising:
(a) a nucleotide sequence encoding a polypeptide having at least 90% sequence identity, based on the Clustal method of alignment, when compared to the sequence set forth in SEQ ID NO:20, or (b) a full-length complement of the nucleotide sequence of (a).
22 . The isolated polynucleotide of claim 21 , wherein the polypeptide has at least 95% sequence identity, based on the Clustal method of alignment, when compared to the sequence set forth in SEQ ID NO:20.
23 . The isolated polynucleotide of claim 22 encoding the sequence set forth in SEQ ID NO:20.
24 . The isolated polynucleotide of claim 23 , wherein the nucleotide sequence comprises the sequence set forth in SEQ ID NO:19.
25 . A vector comprising the isolated polynucleotide of claim 21 .
26 . A recombinant DNA construct comprising the isolated polynucleotide of claim 21 operably linked to a regulatory sequence.
27 . A cell comprising the recombinant DNA construct of claim 26 .
28 . A plant comprising the recombinant DNA construct of claim 26 .
29 . A seed comprising the recombinant DNA construct of claim 26 .
30 . A method for transforming a cell, comprising transforming a cell with the isolated polynucleotide of claim 21 .
31 . A method for producing a plant comprising transforming a plant cell with the isolated polynucleotide of claim 21 and regenerating a plant from the transformed plant cell.
32 . An isolated polypeptide having at least 90% sequence identity, based on the Clustal method of alignment, when compared to the sequence set forth in SEQ ID NO:20.
33 . The isolated polypeptide of claim 32 , wherein the isolated polypeptide has at least 95% sequence identity, based on the Clustal method of alignment, when compared to the sequence set forth in SEQ ID NO:20.
34 . The isolated polypeptide of claim 33 , wherein the isolated polypeptide comprises the amino acid sequence set forth in SEQ ID NO:20.Cited by (0)
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