IP Library Granted Patent US 8,076,141
Granted Patent B2
US 8,076,141 · App. 13/042,531 · Granted Dec 13, 2011

Nucleotide sequences encoding

Assignees: E.I. du Pont de Nemours and Company; Cold Spring Harbor Laboratory
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 8,076,141
App. No.
13/042,531
Granted
Dec 13, 2011
Kind
B2
Abstract

The invention relates to the isolation and characterization of a maize gene, RAMOSA3 (RA3), responsible for meristem development and inflorescence development including branching. The gene, gene product, and regulatory regions may be used to manipulate branching, meristem growth, inflorescence development and arrangement, and ultimately to improve yield of plants. The invention includes the gene and protein product as well as the use of the same for temporal and spatial expression in transgenic plants to alter plant morphology and affect yield in plants. The invention also includes the gene and protein product for SISTER OF RAMOSA3 (SRA).

Claims (14)

1. An isolated polynucleotide comprising:

(a) a nucleic acid sequence encoding a polypeptide having trehalose-6-phosphate phosphatase activity, wherein the polypeptide has an amino acid sequence comprising SEQ ID NO: 69; or

(b) a complement of the nucleotide sequence, wherein the complement and the nucleotide sequence consist of the same number of nucleotides and are 100% complementary.

2. A recombinant DNA construct comprising the polynucleotide of claim 1 operably linked to a promoter that is functional in a plant.

3. A method for altering trehalose-6-phosphate phosphatase activity in a plant, comprising:

(a) introducing into a regenerable plant cell the recombinant DNA construct of claim 2 to produce a transformed plant cell; and

(b) regenerating a transgenic plant from said transformed plant cell, wherein said transgenic plant comprises in its genome said recombinant DNA construct and wherein said transgenic plant exhibits an alteration in trehalose-6-phosphate phosphatase activity, when compared to a control plant not comprising said recombinant DNA construct.

4. The method of claim 3 , further comprising (c) obtaining a progeny plant derived from said transgenic plant, wherein said progeny plant comprises in its genome the recombinant DNA construct.

5. The method of claim 3 , wherein the transgenic plant exhibits an increase in trehalose-6-phosphate phosphatase activity.

6. A method for increasing environmental stress tolerance of a plant, comprising:

(a) introducing into a regenerable plant cell the recombinant DNA construct of claim 2 to produce a transformed plant cell; and

(b) regenerating a transgenic plant from said transformed plant cell, wherein said transgenic plant comprises in its genome said recombinant DNA construct and wherein said transgenic plant exhibits an increase in environmental stress tolerance, when compared to a control plant not comprising said recombinant DNA construct.

7. The method of claim 6 , further comprising (c) obtaining a progeny plant derived from said transgenic plant, wherein said progeny plant comprises in its genome the recombinant DNA construct.

8. The method of claim 6 , wherein said environmental stress is drought, and wherein said transgenic plant exhibits an increase in drought tolerance.

Continuity (6)
Division 12498699 · Jul 7, 2009
Division 11942036 · Nov 19, 2007
Division 11327740 · Jan 6, 2006
Provisional Application 60642273 · Jan 7, 2005
Provisional Application 60739857 · Nov 23, 2005
Related Publication 20110162108A1 · Jun 30, 2011