US2003177524A1PendingUtilityA1
Gene involved in pyrimidine biosynthesis in plants
Priority: Sep 30, 1999Filed: May 7, 2003Published: Sep 18, 2003
Est. expirySep 30, 2019(expired)· nominal 20-yr term from priority
C12N 15/8262C12N 9/88C12N 15/8261Y02A40/146
59
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Claims
Abstract
This invention relates to an isolated nucleic acid fragment encoding an OMP decarboxylase. The invention also relates to the construction of a chimeric gene encoding all or a portion of the OMP decarboxylase, in sense or antisense orientation, wherein expression of the chimeric gene results in production of altered levels of the OMP decarboxylase in a transformed host cell.
Claims
exact text as granted — not AI-modifiedWhat is claimed is:
1 . An isolated polynucleotide that encodes a polypeptide of at least 200 amino acids having a sequence identity of at least 85% based on the Clustal method of alignment when compared to a polypeptide selected from the group consisting of SEQ ID NOs:6, 8, 10, and 12.
2 . A polynucleotide sequence of claim 1 , wherein sequence identity is at least 90%.
3 . A polynucleotide sequence of claim 1 , wherein sequence identity is at least 95%.
4 . The polynucleotide of claim 1 wherein the polynucleotide encodes a polypeptide selected from the group consisting of SEQ ID NOs:6, 8, 10 and 12.
5 . The polynucleotide of claim 1 , wherein the polynucleotide comprises a nucleotide sequence selected from the group consisting of SEQ ID NO:5, 7, 9 and 11.
6 . The polynucleotide of claim 1 , wherein the polypeptide is an OMP decarboxylase.
7 . An isolated complement of the polynucleotide of claim 1 , wherein (a) the complement and the polynucleotide consist of the same number of nucleotides, and (b) the nucleotide sequences of the complement and the polynucleotide have 100% complementarity.
8 . An isolated nucleic acid molecule that (1) comprises at least 800 nucleotides and (2) remains hybridized with the isolated polynucleotide of claim 24 under a washing condition of 0.1×SSC, 0.1% SDS, and 65° C.
9 . A cell comprising the polynucleotide of claim 1 .
10 . The cell of claim 9 , wherein the cell is selected from the group consisting of a yeast cell, a bacterial cell and a plant cell.
11 . A transgenic plant comprising the polynucleotide of claim 1 .
12 . A method for transforming a cell comprising introducing into a cell the polynucleotide of claim 1 .
13 . A method for producing a transgenic plant comprising (a) transforming a plant cell with the polynucleotide of claim 1 , and (b) regenerating a plant from the transformed plant cell.
14 . A method for producing a polynucleotide fragment comprising (a) selecting a nucleotide sequence comprised by the polynucleotide of claim 1 , and (b) synthesizing a polynucleotide fragment containing the nucleotide sequence.
15 . The method of claim 14 , wherein the fragment is produced in vivo.
16 . An isolated polypeptide comprising (a) at least 200 amino acids, and (b) a first amino acid sequence, wherein the first amino acid sequence and a second amino acid sequence have a sequence identity of at least 85%, and wherein the second amino acid is selected from the group consisting of SEQ ID NOs:6, 8, 10, and 12.
17 . The polypeptide of claim 16 , wherein the sequence identity is at least 90%.
18 . The polypeptide of claim 16 , wherein the sequence identity is at least 95%.
19 . The polypeptide of claim 16 wherein the polypeptide has a sequence selected from the group consisting of SEQ ID NOs:6, 8, 10, and 12.
20 . The polypeptide of claim 16 , wherein the polypeptide is an OMP decarboxylase.
21 . A chimeric gene comprising the polynucleotide of claim 1 operably linked to at least one suitable regulatory sequence.
22 . A method for altering the level of OMP decarboxylase.expression in a host cell, the method comprising:
(a) Transforming a host cell with the chimeric gene of claim 21; and (b) Growing the transformed cell in step (a) under condistions suitable for the expression of the chimeric gene.Join the waitlist — get patent alerts
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