MSCA1 nucleotide sequences impacting plant male fertility and method of using same

US9803215B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-9803215-B2
Application numberUS-201414543092-A
CountryUS
Kind codeB2
Filing dateNov 17, 2014
Priority dateAug 3, 2007
Publication dateOct 31, 2017
Grant dateOct 31, 2017

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Abstract

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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.

First claim

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What is claimed is: 1. A method of maintaining a homozygous recessive condition of a male sterile plant, the method comprising: (a) providing a first plant comprising homozygous recessive alleles of a Msca1 gene, wherein said plant is male sterile; (b) providing a second plant comprising homozygous recessive alleles of the Msca1 gene and a construct in the hemizygous condition, the construct comprising: (i) a first nucleotide sequence comprising the Msca1 nucleotide sequence, that when expressed in the first plant would restore male fertility; (ii) a second nucleotide sequence that when expressed inhibits the function or formation of viable male gametes in the second plant, such that viable male gametes are produced in the second plant containing the recessive alleles of Msca1 and that do not contain the construct; and (c) fertilizing the first plant with the male gametes of the second plant to produce progeny which maintain the homozygous recessive condition of the first plant. 2. The method of claim 1 , wherein the first nucleotide sequence is operably linked to a third nucleotide sequence regulating expression of the first nucleotide sequence. 3. The method of claim 2 , wherein the third nucleotide sequence functions only in the presence of an inducing substance or condition. 4. The method of claim 1 , wherein the second nucleotide sequence is operably linked to a third nucleotide sequence, the third nucleotide sequence directing expression preferentially to male gametes. 5. The method of claim 4 , wherein the second nucleotide sequence is selected from the group consisting of the nucleotide sequence of the DAM methylase gene, Zea mays alpha amylase gene, and a cytotoxin encoding gene. 6. The method of claim 4 , wherein the third nucleotide sequence is selected from the group consisting of the regulatory region 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 , further comprising a third nucleotide sequence encoding a product, the expression of which is capable of being used 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 red fluorescent gene, cyan fluorescent protein gene, yellow fluorescent protein gene, luciferase gene, green fluorescent protein gene, anthocyanin p1 gene and phosphinothricin acetyltransferase encoding gene. 9. The method of claim 7 , further comprising selecting for said second plant by identifying plants having said construct. 10. A method of maintaining a homozygous recessive condition of a first plant when crossing the first plant to a second plant, the method comprising: (a) providing a first plant comprising homozygous recessive alleles; of a Msca1 gene, the expression of which results in male sterility; (b) providing a second plant comprising homozygous recessive alleles of the Msca1 gene and a construct in a hemizygous condition, the construct comprising: (i) a first nucleotide sequence comprising the Msca1 nucleotide sequence, that when expressed in the first plant would restore male fertility; (ii) a second nucleotide sequence selected from the group consisting of the sequence of the DAM methylase gene, Zea mays alpha amylase gene, and a cytotoxin encoding gene; (iii) a third nucleotide sequence operably linked to the second nucleotide sequence directing expression to plant male gametes, such that viable male gametes are produced in the second plant containing the recessive alleles, and that do not contain the construct; and (c) fertilizing the first plant with the male gametes of the second plant to produce progeny which are male sterile and maintain the homozygous recessive condition of the first plant. 11. The method of claim 10 , further comprising a fourth nucleotide sequence encoding a product capable of being used for selection of plant cells containing the construct. 12. The method of claim 11 wherein the fourth nucleotide sequence is selected from the group consisting of red fluorescent gene, cyan fluorescent protein gene, yellow fluorescent protein gene, luciferase gene, green fluorescent protein gene, anthocyanin p1 gene and phosphinothricin acetyltransferase encoding gene. 13. The method of claim 10 wherein the third nucleotide sequence is selected from the group consisting of a regulatory region from 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 1 wherein the first nucleotide sequence is selected from the group consisting of: (a) SEQ ID NO: 1; (b) a nucleic acid sequence encoding the amino acid sequence comprising SEQ ID NO: 2; (c) SEQ ID NO: 16; (d) a sequence having at least 90% identity to the full length of any of the foregoing sequences wherein the sequence impacts male fertility in a plant; and (e) a sequence which hybridizes to the full length complement of any of the sequences of parts (a-c) under highly stringent conditions of a wash of 0.1 SSC, 0.1% (w/v) SDS at 65° C. wherein the sequence impacts male fertility in a plant. 15. The method of claim 14 , wherein the first nucleotide sequence is operably linked to a third nucleotide sequence regulating expression of the first nucleotide sequence. 16. The method of claim 15 wherein the third nucleotide sequence is selected from the group consisting of: (a) SEQ ID NO: 15; (b) SEQ ID NO:18; (c) bases 1-1109 of SEQ ID NO: 15; (d) bases 1-609 of SEQ ID NO: 15; and (e) a functional fragment of a nucleotide sequence selected from the group consisting of SEQ ID NO: 15 and SEQ ID NO: 18, wherein said fragment is required for male tissue preferred expression. 17. The method of claim 16 , wherein the second nucleotide sequence is operably linked to a fourth nucleotide sequence, the fourth nucleotide sequence directing expression preferentially to male gametes. 18. The method of claim 17 , wherein the second nucleotide sequence is selected from the group consisting of the nucleotide sequence of the DAM methylase gene, Zea mays alpha amylase gene, and a cytotoxin encoding gene. 19. The method of claim 17 , wherein the fourth nucleotide sequence is selected from the group consisting of the regulatory region 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. 20. The method of claim 16 , wherein said construct further comprises a fifth nucleotide sequence encoding a product capable of being used for selection of plant cells having the construct. 21. The method of claim 20 , further comprising selecting for said second plant by identifying plants having said construct. 22. The method of claim 15 , wherein the third nucleotide sequence functions only in the presence of an inducing substance or condition. 23. The method of claim 14 , wherein the second nucleotide sequence is linked to a third nucleotide sequence, the third nucleotide sequence directing expression preferentially to male gametes. 24. The method of claim 23 , wherein the second nucleotide sequence is selected from the group consisting of the nucleotid

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What does patent US9803215B2 cover?
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.
Who is the assignee on this patent?
Pioneer Hi Bred Int, Du Pont, Pioneer Hi Bred Int
What technology area does this patent fall under?
Primary CPC classification C12N15/8289. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Oct 31 2017 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).