Compositions and methods for improving crop yields through trait stacking

Patent metadata

Field	Value
Publication number	US-12116586-B2
Application number	US-202217820205-A
Country	US
Kind code	B2
Filing date	Aug 16, 2022
Priority date	Feb 15, 2018
Publication date	Oct 15, 2024
Grant date	Oct 15, 2024

Abstract

The present disclosure provides modified, transgenic, or genome edited/mutated corn plants that are semi-dwarf and have one or more improved ear traits relative to a control plant, such as increase in ear diameter, single kernel weight, ear fresh weight, ear area, ear volume, ear length, number of kernels per ear, and yield. The modified, transgenic, or genome edited/mutated corn plants comprise a transgene encoding one or more MADS-box polypeptides and have a reduced expression of one or more GA20 or GA3 oxidase genes. Also provided are methods for producing the modified, transgenic, or genome edited/mutated corn plants.

First claim

The invention claimed is:

1. A method for producing a transgenic corn plant, the method comprising:
(I) introducing into a corn cell (i) a first recombinant expression cassette comprising a first heterologous plant-expressible promoter operably linked to a transcribable DNA sequence encoding a non-coding RNA for suppression of one or more gibberellic acid 20 (GA20) oxidase genes, wherein the non-coding RNA comprises a targeting sequence that is (a) at least 95% complementary to at least 19 consecutive nucleotides of a first mRNA molecule encoding a first endogenous GA20 oxidase protein that has at least 95% amino acid sequence identity to the amino acid sequence as set forth in SEQ ID NO: 9, and (b) at least 95% complementary to at least 19 consecutive nucleotides of a second mRNA molecule encoding a second endogenous GA20 oxidase protein that has at least 95% amino acid sequence identity to the amino acid sequence as set forth in SEQ ID NO: 15, and (ii) a second recombinant expression cassette comprising a DNA sequence encoding a MADS-box polypeptide that has at least 95% amino acid sequence identity to the amino acid sequence as set forth in SEQ ID NO: 168; and
(II) regenerating or developing a transgenic corn plant from the corn cell, wherein the transgenic corn plant comprises the first and second recombinant expression cassettes, and wherein expression of said non-coding RNA and said MADS-box polypeptide in said transgenic corn plant results in a semi-dwarf phenotype, and an increase in one or more improved ear trait selected from the group consisting of ear diameter, single kernel weight, ear fresh weight, ear area, ear volume, ear length, kernels per ear, yield, grain yield estimate, broad acreage yield, ear dry weight, and ear tip void, as compared to a control wild-type corn plant grown under comparable conditions.

2. The method of claim 1 , wherein the transcribable DNA sequence encoding said non-coding RNA comprises a nucleotide sequence that is 100% identical or complementary to at least 15 consecutive nucleotides of SEQ ID NO: 39.

3. A method for producing a transgenic corn plant, the method comprising:
(I) crossing a first transgenic corn plant with a second transgenic corn plant, wherein the first transgenic corn plant comprises a first recombinant expression cassette comprising a first heterologous plant-expressible promoter operably linked to a transcribable DNA sequence encoding a non-coding RNA for suppression of one or more gibberellic acid 20 (GA20) oxidase genes, wherein the non-coding RNA comprises a targeting sequence that is (a) at least 95% complementary to at least 19 consecutive nucleotides of a first mRNA molecule encoding a first endogenous GA20 oxidase protein that has at least 95% amino acid sequence identity to the amino acid sequence as set forth in SEQ ID NO: 9, and (b) at least 95% complementary to at least 19 consecutive nucleotides of a second mRNA molecule encoding a second endogenous GA20 oxidase protein that has at least 95% amino acid sequence identity to the amino acid sequence as set forth in SEQ ID NO: 15, and wherein the expression of one or more endogenous GA20 oxidase genes is reduced in the first transgenic corn plant as compared to a control wild-type corn plant grown under comparable conditions, and wherein the second transgenic corn plant comprises a second recombinant expression cassette comprising a DNA sequence encoding a MADS-box polypeptide that has at least 95% amino acid sequence identity to the amino acid sequence as set forth in SEQ ID NO: 168; and
(II) producing a transgenic progeny corn plant comprising the first and second recombinant expression cassettes and that has the reduced expression of the one or more endogenous GA20 oxidase genes, and increased expression of said MADS-box polypeptide as compared to a control wild-type corn plant grown under comparable conditions, and wherein expression of said non-coding RNA and said MADS-box polypeptide in said transgenic progeny corn plant results in a semi-dwarf phenotype, and an increase in one or more improved ear trait selected from the group consisting of ear diameter, single kernel weight, ear fresh weight, ear area, ear volume, ear length, kernels per ear, yield, grain yield estimate, broad acreage yield, ear dry weight, and ear tip void, as compared to a control wild-type corn plant grown under comparable conditions.

4. The method of claim 3 , wherein the first transgenic corn plant and the transgenic progeny corn plant comprise a transcribable DNA sequence encoding said non-coding RNA comprising a nucleotide sequence that is 100% identical or complementary to at least 15 consecutive nucleotides of SEQ ID NO: 39.

5. The method of claim 1 , wherein the transcribable DNA sequence comprised in the first recombinant expression cassette or the DNA sequence comprised in the second recombinant expression cassette is operably linked to a heterologous plant-expressible promoter selected from the group consisting of a vascular promoter, a rice tungro bacilliform virus (RTBV) promoter, a leaf promoter, and a constitutive promoter.

6. The method of claim 1 , wherein the introducing is via site-directed integration using a site-specific nuclease, Agrobacterium -mediated transformation, or particle bombardment.

7. The method of claim 1 , wherein the first and second recombinant expression cassettes are stably integrated into the genome of the transgenic corn plant produced in step (II).

8. The method of claim 3 , wherein the first or the second recombinant expression cassette is operably linked to a heterologous plant-expressible promoter selected from the group consisting of a vascular promoter, a rice tungro bacilliform virus (RTBV) promoter, a leaf promoter, and a constitutive promoter.

9. The method of claim 3 , wherein the first and the second transgenic corn plants are obtained via site-directed integration using a site-specific nuclease, Agrobacterium -mediated transformation, or particle bombardment.

10. The method of claim 1 , further comprising selecting a transgenic progeny corn plant of said transgenic corn plant of step (II) that is semi-dwarf and has increased crown root lateral root density rating at the V12 stage and increased root dry weight as compared to a control wild-type corn plant grown under comparable conditions.

11. The method of claim 3 , further comprising selecting a transgenic progeny corn plant that is semi-dwarf and has increased crown root lateral root density rating at the V12 stage and increased root dry weight as compared to a control wild-type corn plant grown under comparable conditions.

Assignees

• Monsanto Technology Llc

Inventors

• Dietrich Charles R
• Ivleva Natalia
• Slewinski Thomas L

Classifications

• C12N15/8218

  Antisense, co-suppression, viral induced gene silencing [VIGS], post-transcriptional induced gene silencing [PTGS] · CPC title

• C12N15/8297

  Gibberellins; GA3 · CPC title

• Y02A40/146

  Genetically Modified [GMO] plants, e.g. transgenic plants · CPC title

• C12N15/8261 Primary

  with agronomic (input) traits, e.g. crop yield · CPC title