IP Library Granted Patent US 10,731,171
Granted Patent B2
US 10,731,171 · App. 16/272,033 · Granted Aug 4, 2020

Plant promoter for transgene expression

Inventors: John Davies (Indianapolis, IN); David Mann (Indianapolis, IN); James Patrick Connell (Indianapolis, IN); William T. Beeson, IV (Indianapolis, IN)
Assignee: Dow AgroSciences LLC
C12N15/8216C12N15/8229C12N15/8233
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Quick Facts
Patent No.
US 10,731,171
App. No.
16/272,033
Granted
Aug 4, 2020
Kind
B2
Abstract

This disclosure concerns compositions and methods for promoting transcription of a nucleotide sequence in a plant or plant cell, employing a promoter from a Zea mays KN1 gene. Some embodiments relate to a promoter from a Zea mays KN1 gene that functions in plants to promote transcription of operably linked nucleotide sequences.

Claims (25)

1. A gene expression cassette comprising a promoter operably linked to a heterologous nucleic acid, wherein the promoter comprises a polynucleotide comprising a sequence identity of at least 97% to SEQ ID NO:1.

2. The gene expression cassette of claim 1 , wherein the polynucleotide further comprises an intron.

3. The gene expression cassette of claim 1 , wherein the polynucleotide further comprises a 5′ UTR.

4. The gene expression cassette of claim 1 , wherein the heterologous nucleic acid is operably linked to a 3′ UTR.

5. The gene expression cassette of claim 1 , wherein the operably linked heterologous nucleic acid encodes a polypeptide or a small RNA gene.

6. The gene expression cassette of claim 1 , wherein the heterologous nucleic acid is selected from the group consisting of a heterologous nucleic acid conferring insecticidal resistance, a heterologous nucleic acid conferring herbicide tolerance, a heterologous nucleic acid conferring nitrogen use efficiency, a heterologous nucleic acid conferring water use efficiency, a heterologous nucleic acid conferring nutritional quality, a heterologous nucleic acid encoding a DNA binding protein, and a heterologous nucleic acid encoding a selectable marker.

7. A recombinant vector comprising the gene expression cassette of claim 1 , wherein the vector is selected from the group consisting of a plasmid, a cosmid, a bacterial artificial chromosome, a virus, and a bacteriophage.

8. A transgenic cell comprising the gene expression cassette of claim 1 .

9. The transgenic cell of claim 8 , wherein the transgenic cell is a transgenic plant cell.

10. A transgenic plant comprising the transgenic cell of claim 8 .

11. The transgenic plant of claim 10 , wherein the transgenic plant is a monocotyledonous plant or dicotyledonous plant.

12. The transgenic plant of claim 11 , wherein the monocotyledonous plant is selected from the group consisting of a maize plant, a rice plant, and a wheat plant.

13. A transgenic seed from the transgenic plant of claim 10 , wherein the seed comprises the gene expression cassette.

14. The gene expression cassette of claim 10 , wherein the promoter drives expression of the heterologous nucleic acid in reproductive meristematic tissue.

15. The gene expression cassette of claim 1 , wherein the promoter comprises the polynucleotide sequence of nucleotides 1 to 1,407 of SEQ ID NO:1.

16. A method for expressing a coding sequence in a transgenic plant, the method comprising:

a) transforming a plant cell with a gene expression cassette comprising a polynucleotide sequence comprising a sequence identity of at least 97% to SEQ ID NO:1 operably linked to the heterologous coding sequence, which is operably linked to a 3′ untranslated region;

b) isolating the transformed plant cell comprising the gene expression cassette;

c) regenerating a transgenic plant from the transformed plant cell; and,

d) obtaining the transgenic plant, wherein the transgenic plant expresses the coding sequence.

17. A method for manufacturing a synthetic polynucleotide sequence comprising a sequence identity of at least 97% to SEQ ID NO:1, the method comprising:

a) isolating a nucleic acid comprising a polynucleotide sequence comprising SEQ ID NO:1;

b) producing a plurality of oligonucleotide primer sequences, wherein the oligonucleotide primer sequences bind to the nucleic acid under stringent hybridization conditions;

c) ligating the plurality of oligonucleotide primer sequences to synthesize a synthetic polynucleotide sequence; and,

d) sequencing the resulting synthetic polynucleotide to confirm that it comprises at least 97% identity to SEQ ID NO:1.

Assignments (2)
CHANGE OF NAME Recorded Nov 8, 2021
From: DOW AGROSCIENCES LLC
To: CORTEVA AGRISCIENCE LLC
Reel/Frame 058044/0184 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 16, 2019
From: DAVIES, JOHN; MANN, DAVID; BEESON, WILLIAM T., IV; CONNELL, JAMES PATRICK
To: DOW AGROSCIENCES LLC
Reel/Frame 048894/0141 →