IP Library Granted Patent US 11,236,350
Granted Patent B2
US 11,236,350 · App. 16/139,112 · Granted Feb 1, 2022

Plant promoter for transgene expression

Inventors: Sandeep Kumar (Johnston, IA); Sara Bennett (Indianapolis, IN); Andrew J. Bowling (Zionsville, IN); Alicia Walker (Indianapolis, IN); Cory M. Larsen (Zionsville, IN); Heather Pence (Indianapolis, IN); Staci Weaver (Indianapolis, IN); Ronnie Hampton, Jr. (Indianapolis, IN)
Assignee: Corteva Agriscience LLC
C12N15/8233A01H6/604
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Quick Facts
Patent No.
US 11,236,350
App. No.
16/139,112
Granted
Feb 1, 2022
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 Glycine max egg cell gene. Some embodiments relate to a promoter or a 5′ UTR from a Glycine max egg cell gene that functions in plants to promote transcription of operably linked nucleotide sequences. Other embodiments relate to a 3′ UTR or a terminator from a Glycine max egg cell gene that functions in plants to promote transcription of operably linked nucleotide sequences.

Claims (23)

1. A nucleic acid vector comprising a promoter operably linked to:

a) a non-natural synthetic polylinker sequence;

b) a heterologous coding sequence; or

c) a combination of a) and b); wherein said promoter comprises a polynucleotide sequence that has at least 99% sequence identity with SEQ ID NO:2, and wherein said promoter has ovule preferred tissue expression.

2. The nucleic acid vector of claim 1 , wherein said promoter is 1,089 bp in length.

3. The nucleic acid vector of claim 1 , wherein said promoter consists of a polynucleotide sequence that has at least 99% sequence identity with SEQ ID NO:2.

4. The nucleic acid vector of claim 1 , wherein said promoter is operably linked to a heterologous coding sequence.

5. The nucleic acid vector of claim 4 , wherein the heterologous coding sequence encodes a selectable marker protein, an insecticidal resistance protein, a herbicide tolerance protein, a nitrogen use efficiency protein, a water use efficiency protein, a small RNA molecule, a nutritional quality protein, or a DNA binding protein.

6. The nucleic acid vector of claim 4 , further comprising a terminator polynucleotide sequence operably linked to the heterologous coding sequence.

7. The nucleic acid vector of claim 4 , further comprising a 3′ untranslated polynucleotide sequence operably linked to the heterologous coding sequence.

8. The nucleic acid vector of claim 1 , further comprising a 5′ untranslated polynucleotide sequence operably linked to the promoter.

9. The nucleic acid vector of claim 1 , further comprising an intron sequence operably linked to the promoter.

10. A transgenic plant comprising a polynucleotide sequence that has at least 99% sequence identity with SEQ ID NO:2 operably linked to a heterologous coding sequence, wherein said promoter has ovule preferred tissue expression.

11. The transgenic plant of claim 10 , wherein said plant is selected from the group consisting of Zea mays , wheat, rice, sorghum, oats, rye, bananas, sugar cane, Glycine max , cotton, Arabidopsis , tobacco, sunflower, and canola.

12. The transgenic plant of claim 11 , wherein said plant is Glycine max.

13. The transgenic plant of claim 10 , wherein the heterologous coding sequence is inserted into the genome of said plant.

14. The transgenic plant of claim 10 , further comprising a 3′ untranslated sequence operably linked to the heterologous coding sequence.

15. The transgenic plant of claim 10 , wherein said polynucleotide sequence is 1,089 bp in length.

16. A method for producing a transgenic plant cell, the method comprising the steps of:

a) transforming a plant cell with a gene expression cassette comprising a Glycine max egg cell promoter, wherein the Glycine max egg cell promoter comprises a polynucleotide sequence that has at least 99% sequence identity with SEQ ID NO:2, operably linked to at least one polynucleotide sequence of interest;

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

c) producing a transgenic plant cell comprising the Glycine max egg cell promoter of claim 1 operably linked to at least one polynucleotide sequence of interest, and wherein said promoter has ovule preferred tissue expression.

17. A method for expressing a polynucleotide sequence of interest in a plant cell, the method comprising introducing into the plant cell a polynucleotide sequence of interest operably linked to a Glycine max egg cell promoter, wherein the Glycine max egg cell promoter comprises a polynucleotide sequence that has at least 99% sequence identity with SEQ ID NO:2, and wherein said promoter has ovule preferred tissue expression.

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 Sep 24, 2018
From: KUMAR, SANDEEP; BENNETT, SARA; BOWLING, ANDREW J.; WALKER, ALICIA; LARSEN, CORY M.; PENCE, HEATHER; WEAVER, STACI; HAMPTON, RONNIE, JR.
To: DOW AGROSCIENCS LLC
Reel/Frame 046947/0568 →