Fertility gene and use thereof
The present disclosure relates to a fertility gene and the use thereof, and relates to the biotechnology field, particularly to a method of plant hybrid breeding including creation of a sterile line and preparation of hybrid seeds, more particularly to a fertility gene FL2, a mutant thereof and use thereof in hybrid breeding.
1. A method of producing a male sterile rice plant having a homozygous recessive male sterility gene, said method comprising:
(a) providing a first plant comprising a recessive male sterility gene in a homozygous state, wherein the recessive male sterility gene comprises nucleotide sequence of SEQ ID NO:7, and wherein the first plant is male sterile;
(b) introducing a construct into the plant of (a) to form a second plant, wherein the second plant comprises the recessive male sterility gene in a homozygous state and the construct in a hemizygous state, and wherein the construct comprises:
i) a first nucleotide sequence comprising a sequence encoding the amino acid sequence of SEQ ID NO: 2 or 6, wherein the first nucleotide sequence is operably linked to a first promoter that allows expression of the first nucleotide sequence in the second plant, wherein expression of the first nucleotide sequence restores male fertility; and
ii) a second nucleotide sequence that inhibits the formation of gametes of male fertility when expressed in the second plant, wherein the second nucleotide sequence is selected from the group consisting of a DAM methylase encoding sequence and a cytotoxin encoding sequence and wherein the second nucleotide sequence is operably linked to a second promoter that allows expression of the second nucleotide sequence in the second plant; and
(c) fertilizing another plant of (a) with the male gametes of the second plant to produce an offspring having the recessive male sterility gene in a homozygous state.
2. The method of claim 1 , wherein the first nucleotide sequence is the nucleotide sequence of SEQ ID NO:1 or 5.
3. The method of claim 1 , wherein the first promoter comprises SEQ ID NO:3 or SEQ ID NO:9.
4. The method of claim 1 , wherein the first promoter is an inducible promoter.
5. The method of claim 1 , wherein the first promoter is selected from the group consisting of the promoters of the Os10g38050, 5126, Ms26 and Ms45 genes.
6. The method of claim 1 , wherein the second promoter is selected from the group consisting of the promoters of the polygalacturonase 47 gene, Zm13 gene, pectin methylesterase gene, calmodulin binding protein gene, actin depolymerizing factor gene, profilin gene, and sulphated pentapeptide phytosulphokine gene.
7. The method of claim 1 , wherein the construct further comprises a third nucleotide sequence that allows for selection of plant cells having the construct.
8. The method of claim 7 , wherein the third nucleotide sequence is selected from the group consisting of a red fluorescent protein encoding sequence, a cyan fluorescent protein encoding sequence, a yellow fluorescent protein encoding sequence, a luciferase encoding sequence, a green fluorescent protein encoding sequence, an anthocyanin pI encoding sequence and a phosphinothricin acetyltransferase encoding sequence.
9. The method of claim 7 , wherein the third nucleotide sequence is operably linked to a third promoter selected from the group consisting of the promoters of the lipid transfer protein (LTP2) gene, polygalacturonase 47 gene, Zm13 gene, pectin methylesterase gene, calmodulin binding protein gene, actin depolymerizing factor gene, profilin gene, and sulphated pentapeptide phytosulphokine gene.
10. A method of producing seeds from a rice plant having female and male gametes, the method comprising:
self fertilizing a plant, wherein the plant is (1) homozygous for a gene comprising the nucleotide sequence of SEQ ID NO:7 and (2) hemizygous for a construct comprising:
(i) a first nucleotide sequence comprising a sequence encoding the amino acid sequence of SEQ ID NO:2 or 6, wherein the first nucleotide sequence is operably linked to a first promoter that allows expression of the first nucleotide sequence in the plant, wherein expression of the first nucleotide sequence restores male fertility; and
ii) a second nucleotide sequence that inhibits the formation of gametes of male fertility when expressed in the plant, wherein the second nucleotide sequence is selected from the group consisting of a DAM methylase encoding sequence and a cytotoxin encoding encoding sequence, and wherein the second nucleotide sequence is operably linked to a second promoter that allows expression of the second nucleotide sequence in the plant; and
harvesting seeds from the self-fertilized plant.
11. The method of claim 10 , wherein the first nucleotide sequence is the nucleotide sequence of SEQ ID NO:1 or 5.
12. The method of claim 10 , wherein the first promoter is selected from the group consisting of promoters of the Os10g38050, 5126, Ms26 and Ms45 genes.
13. The method of claim 10 , wherein the second promoter is selected from the group consisting of the promoters of the polygalacturonase 47 gene, Zm13 gene, pectin methylesterase gene, calmodulin binding protein gene, actin depolymerizing factor gene, profilin gene, and sulphated pentapeptide phytosulphokine gene.
14. The method of claim 10 , wherein the construct further comprises a third nucleotide sequence that allows for selection of plant cells having the construct.
15. The method of claim 14 wherein the third nucleotide sequence is a red fluorescent protein encoding sequence, a cyan fluorescent protein encoding sequence, a yellow fluorescent protein encoding sequence, a luciferase encoding sequence, a green fluorescent protein encoding sequence, an anthocyanin pI encoding sequence or a phosphinothricin acetyltransferase encoding sequence.
16. The method of claim 15 , wherein the third nucleotide sequence is operably linked to a third promoter selected from the group consisting of the promoters of the lipid transfer protein (LTP2) gene, polygalacturonase 47 gene, Zm13 gene, pectin methylesterase gene, calmodulin binding protein gene, actin depolymerizing factor gene, profilin gene, and sulphated pentapeptide phytosulphokine gene.