Data processing of the maize prolifera genetic sequence
First Claim
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1. An isolated nucleic acid comprising a member selected from the group consisting of:
- (a) a polynucleotide having at least 85% sequence identity, as determined by the BLAST 2.0 algorithm under default parameters, to a polynucleotide encoding a polypeptide selected from the group consisting of SEQ ID NO;
2;
(b) a polynucleotide encoding a polypeptide selected from the group consisting of SEQ ID NO;
2;
(c) a polynucleotide amplified from a Zea mays nucleic acid library using primers which selectively hybridize, under stringent hybridization conditions, to loci within a polynucleotide selected from the group consisting of SEQ ID NO;
1;
(d) a polynucleotide which selectively hybridizes, under stringent hybridization conditions and a wash in 2×
SSC at 50°
C., to a polynucleotide selected from the group consisting of SEQ ID NO;
1;
(e) a polynucleotide selected from the group consisting of SEQ ID NO;
1;
(f) a polynucleotide which is complementary to a polynucleotide of (a), (b), (c), (d), or (e); and
(g) a polynucleotide comprising at least 25 contiguous nucleotides from a polynucleotide of (a), (b), (c), (d), (e), or (f).
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Abstract
The invention provides isolated prolifera nucleic acids and their encoded proteins. The present invention provides methods and compositions relating to altering prolifera levels in plants. The invention further provides recombinant expression cassettes, host cells, transgenic plants, and antibody compositions.
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Citations
18 Claims
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1. An isolated nucleic acid comprising a member selected from the group consisting of:
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(a) a polynucleotide having at least 85% sequence identity, as determined by the BLAST 2.0 algorithm under default parameters, to a polynucleotide encoding a polypeptide selected from the group consisting of SEQ ID NO;
2;
(b) a polynucleotide encoding a polypeptide selected from the group consisting of SEQ ID NO;
2;
(c) a polynucleotide amplified from a Zea mays nucleic acid library using primers which selectively hybridize, under stringent hybridization conditions, to loci within a polynucleotide selected from the group consisting of SEQ ID NO;
1;
(d) a polynucleotide which selectively hybridizes, under stringent hybridization conditions and a wash in 2×
SSC at 50°
C., to a polynucleotide selected from the group consisting of SEQ ID NO;
1;
(e) a polynucleotide selected from the group consisting of SEQ ID NO;
1;
(f) a polynucleotide which is complementary to a polynucleotide of (a), (b), (c), (d), or (e); and
(g) a polynucleotide comprising at least 25 contiguous nucleotides from a polynucleotide of (a), (b), (c), (d), (e), or (f). - View Dependent Claims (2, 3, 4, 5, 6, 7, 8, 9, 10)
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11. A data processing system, comprising:
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data representing at least one genetic sequence;
a genetic identification, analysis, or modeling computer program designed to govern the processing of such data;
a data processor having an output for storing or displaying data processing results, said data processor containing said data and said program and executing instructions according to said program to process said data or a contiguous subsequence thereof; and
wherein said genetic sequence is;
(i) at least 90% sequence identical to a polynucleotide sequence of SEQ ID NO;
1, or (ii) at least 95% sequence identical to a polypeptide sequence of SEQ ID NO;
2, and wherein sequence identity is determined by the GAP algorithm under default parameters. - View Dependent Claims (12, 13, 14, 15, 16, 17, 18)
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Specification