Methods and compositions for the introduction and regulated expression of genes in plants

Patent metadata

Field	Value
Publication number	US-10968458-B2
Application number	US-201715673609-A
Country	US
Kind code	B2
Filing date	Aug 10, 2017
Priority date	Dec 30, 2009
Publication date	Apr 6, 2021
Grant date	Apr 6, 2021

Abstract

Compositions and methods are provided for the introduction and the regulated expression of genes in plants. Compositions include promoter constructs that provide a level of activity useful for the regulated expression of site-specific recombinases, while avoiding premature excision. Further provided are isolated polynucleotides encoding novel babyboom polypeptides, expression cassettes, and plants comprising the same. Methods for the introduction of genes into plants are provided, including methods for plastid transformation and methods for the transformation of tissues from mature seeds and leaves.

First claim

That which is claimed:

1. A method for introducing a polynucleotide of interest into a mature embryo monocot explant of a mature monocot seed, said method comprising:
a) dissecting a mature embryo from a mature monocot seed;
b) making slices of said mature embryo to prepare said mature embryo explant, wherein said mature embryo explant comprises at least leaf primordia;
a) introducing into said mature embryo explant:
i) a heterologous polynucleotide encoding a babyboom cell proliferation factor and expressing said heterologous polynucleotide encoding said babyboom cell proliferation factor; and
ii) a polynucleotide of interest; and

d) regenerating a monocot plant comprising the polynucleotide of interest, wherein the mature embryo monocot explant of the mature monocot seed is not rice.

2. The method of claim 1 , wherein said mature embryo explant further comprises mesocotyl, shoot apical meristem, and root primordia.

3. A method for introducing a polynucleotide of interest into a monocot leaf tissue and regenerating a plant therefrom, said method comprising:
a) excising a leaf segment from a leaf above the first leaf base node;
b) dissecting said leaf fragment into leaf tissue;
c) introducing into said leaf tissue:
i) a heterologous polynucleotide encoding a cell proliferation factor flanked by recombination sites;
ii) an expression cassette comprising a promoter followed by a first attachment B (attB) site, wherein the promoter is selected from the group consisting of:

x) a promoter comprising a nucleotide sequence having the sequence set forth in SEQ ID NO: 29;
y) a promoter comprising a nucleotide sequence having at least 70% sequence identity to the sequence set forth in SEQ ID NO: 29; and
z) a promoter comprising at least 50 contiguous nucleotides of the sequence set forth in SEQ ID NO: 29; and
wherein said first attB site has the nucleotide sequence set forth in SEQ ID NO: 31 operably linked to a polynucleotide encoding a site-specific recombinase that is capable of recognizing and implementing recombination at said recombination sites; and
iii) a polynucleotide of interest;

d) expressing said heterologous polynucleotide encoding said cell proliferation factor;
e) incubating said leaf tissue under conditions to allow for growth of a callus;
f) expressing said polynucleotide encoding said site-specific recombinase, thereby excising said heterologous polynucleotide encoding said cell proliferation factor, and;
g) regenerating a plant from said callus.

4. The method of claim 3 , wherein said cell proliferation factor comprises a babyboom polypeptide.

5. The method of claim 1 , wherein the monocot is selected from the group consisting of: maize, sorghum, and wheat.

6. The method of claim 3 , wherein the monocot is selected from the group consisting of maize, sorghum, sugarcane, rice, and wheat.

7. The method of claim 1 , further comprising introducing into said mature embryo monocot explant an additional heterologous polynucleotide encoding an additional cell proliferation factor and expressing said additional heterologous polynucleotide encoding said additional cell proliferation factor.

8. The method of claim 7 , wherein said additional cell proliferation factor is selected from the group consisting of LEAFY COTYLEDON1 (LEC1), Knotted-1 (Kn1), and WUSCHEL.

9. The method of claim 1 , further comprising excising said heterologous polynucleotide encoding said babyboom cell proliferation factor.

10. The method of claim 7 , further comprising excising said additional heterologous polynucleotide encoding said additional cell proliferation factor.

11. The method of claim 3 , further comprising introducing into said leaf tissue an additional heterologous polynucleotide encoding an additional cell proliferation factor flanked by recombination sites and expressing said additional heterologous polynucleotide encoding said additional cell proliferation factor.

12. The method of claim 11 , wherein said additional cell proliferation factor is selected from the group consisting of LEAFY COTYLEDON1 (LEC1), Knotted-1 (Kn1), and WUSCHEL.

13. The method of claim 3 , further comprising excising said heterologous polynucleotide encoding said cell proliferation factor.

14. The method of claim 11 , further comprising excising said additional heterologous polynucleotide encoding said additional cell proliferation factor.

Assignees

• Du Pont
• Pioneer Hi Bred Int

Inventors

• Gordon-Kamm William James
• Klein Theodore Mitchell
• Lowe Keith S
• Mcbride Kevin E
• Scelonge Christopher Jay
• Wang Ning

Classifications

• C12N15/8213 Primary

  Targeted insertion of genes into the plant genome by homologous recombination · CPC title

• C12N15/8262

  involving plant development · CPC title

• C12N15/8241 Primary

  Phenotypically and genetically modified plants via recombinant DNA technology · CPC title

• C12N15/8216

  Methods for controlling, regulating or enhancing expression of transgenes in plant cells · CPC title