Msca1 nucleotide sequences impacting plant male fertility and method of using same
View Patent ↗Nucleotide sequences of a Msca1 gene, critical to male fertility in plants are described, with DNA molecule and amino acid sequences set forth. Promoter sequences and their essential regions are also identified. The nucleotide sequences are useful in impacting male fertility in plants.
1. An isolated nucleotide sequence that is critical to male fertility in a plant, said nucleotide sequence comprising a nucleic acid sequence selected from the group consisting of:
(a) SEQ ID NO: 16;
(b) a nucleic acid sequence having at least 90% identity to the full length of SEQ ID NO: 16 wherein the sequence is critical to male fertility in a plant;
(c) a nucleic acid sequence having at least 95% identity to the full length of SEQ ID NO: 16 wherein the sequence is critical to male fertility in a plant; and
(d) a nucleic acid sequence which hybridizes to the full length complement of SEQ ID NO: 16 under highly stringent conditions of a wash of 0.1 SSC, 0.1% (w/v) SDS at 65° C. wherein the sequence is critical to male fertility in a plant.
2. An isolated nucleotide sequence comprising SEQ ID NO: 16.
3. A plant cell comprising the nucleotide sequence of claim 1 .
4. A plant comprising the nucleotide sequence of claim 1 .
5. An expression vector comprising the nucleotide sequence of claim 1 .
6. A method of impacting male fertility in a plant, said method comprising impacting the expression of a first nucleotide sequence in a plant, the first nucleotide sequence selected from the group consisting of:
(a) SEQ ID NO: 16;
(b) a nucleic acid sequence having at least 90% identity to the full length of SEQ ID NO: 16 wherein the sequence is critical to male fertility in a plant;
(c) a nucleic acid sequence having at least 95% identity to the full length of SEQ ID NO: 16 wherein the sequence is critical to male fertility in a plant; and
(d) a nucleic acid sequence which hybridizes to the full length complement of SEQ ID NO: 16 under highly stringent conditions of a wash of 0.1 SSC, 0.1% (w/v) SDS at 65° C. wherein the sequence is critical to male fertility in a plant.
7. The method of claim 6 wherein expression of the first nucleotide sequence is impacted by a method selected from the group consisting of mutagenesis, introduction of a second nucleotide sequence oriented in the antisense direction relative to the first nucleotide sequence, co-suppression, introduction of sequences encoding hairpin formations, and introduction of a second nucleotide sequence which disrupts expression of the first nucleotide sequence.
8. The method of claim 6 wherein impacting the expression of the first nucleotide sequence results in male sterility in the plant.
9. A method of restoring fertility to the male sterile plant produced by the method of claim 8 , comprising introducing into the male sterile plant a second nucleotide sequence comprising a nucleic acid sequence selected from the group consisting of:
(a) SEQ ID NO: 16;
(b) a nucleic acid sequence encoding the amino acid sequence comprising SEQ ID NO: 17;
(c) a nucleic acid sequence having at least 90% identity to the full length of any of the foregoing sequences wherein the sequence is critical to male fertility in a plant;
(d) a nucleic acid sequence having at least 95% identity to the full length of any of the sequences in parts (a) or (b) wherein the sequence is critical to male fertility in a plant; and
(e) a nucleic acid sequence which hybridizes to the full length complement of any of the sequences in parts (a) or (b) under highly stringent conditions of a wash of 0.1 SSC, 0.1% (w/v) SDS at 65° C. wherein the sequence is critical to male fertility in a plant.
10. The method of claim 6 wherein the expression of the first nucleotide sequence is prevented, and further comprising introducing into the plant a second nucleotide sequence linked to an inducible promoter wherein the second nucleotide sequence is selected from the group consisting of:
(a) SEQ ID NO: 16;
(b) a nucleic acid sequence encoding the amino acid sequence comprising SEQ ID NO: 17;
(c) a nucleic acid sequence having at least 90% identity to the full length of any of the foregoing sequences wherein the sequence is critical to male fertility in a plant;
(d) a nucleic acid sequence having at least 95% identity to the full length of any of the sequences in parts (a) or (b) wherein the sequence is critical to male fertility in a plant; and
(e) a nucleic acid sequence which hybridizes to the full length complement of any of the sequences in parts (a) or (b) under highly stringent conditions of a wash of 0.1 SSC, 0.1% (w/v) SDS at 65° C. wherein the sequence is critical to male fertility in a plant;
such that the plant is constitutively male sterile and fertility is induced by inducing the promoter.
11. The method of restoring fertility to the constitutively male sterile plant produced by the method of claim 10 , further comprising exposing the constitutively male sterile plant to an inducing substance so that the plant becomes male fertile.
12. The method of claim 11 wherein the inducing substance is a herbicide.
13. A method of producing hybrid seed, comprising:
(a) planting in cross-pollinating juxtaposition, a first seed from a selected male fertile parent line and a second seed selected from a female parent line having male sterility produced according to the method of claim 8 ;
(b) cross-pollinating the male sterile female plant with pollen from the male fertile plant; and
(c) harvesting seed from the male sterile female plant.
14. The method of claim 13 wherein the female parent line is male sterile as a result of mutation to the first nucleotide sequence, and wherein said mutant nucleotide sequence is dominant, further comprising;
(d) growing the hybrid seed to produce a third male sterile parent plant; producing a fourth parent plant comprising one or more genes controlling a desired gene trait, and
(e) cross-fertilizing the third and fourth parent plants to produce second hybrid seed.
15. The nucleotide sequence of claim 1 , wherein said sequence is a nucleic acid sequence having at least 95% identity to the full length of SEQ ID NO: 16.
16. The method of claim 6 , wherein said first nucleotide sequence is a nucleic acid sequence having at least 95% identity to the full length of SEQ ID NO: 16.
17. The method of claim 9 , wherein said second nucleotide sequence is a nucleic acid sequence having at least 95% identity to the full length of SEQ ID NO: 16 or a nucleic acid sequence encoding SEQ ID NO: 17.
18. The method of claim 10 , wherein said second nucleotide sequence is a nucleic acid sequence having at least 95% identity to the full length of SEQ ID NO: 16 or a nucleic acid sequence encoding SEQ ID NO: 17.
19. The method of claim 13 , wherein said first nucleotide sequence is a nucleic acid sequence having at least 95% identity to the full length of SEQ ID NO: 16.