26934, a novel cytidine deaminase-like molecule and uses thereof
Abstract
Novel cytidine deaminase-like polypeptides, proteins, and nucleic acid molecules are disclosed. In addition to isolated, full-length cytidine deaminase-like proteins, the invention further provides isolated cytidine deaminase-like fusion proteins, antigenic peptides, and anti-cytidine deaminase-like antibodies. The invention also provides cytidine deaminase-like nucleic acid molecules, recombinant expression vectors containing a nucleic acid molecule of the invention, host cells into which the expression vectors have been introduced, and nonhuman transgenic animals in which an cytidine deaminase-like gene has been introduced or disrupted. Diagnostic, screening, and therapeutic methods utilizing compositions of the invention are also provided.
Claims
exact text as granted — not AI-modifiedThat which is claimed:
1 . An isolated nucleic acid molecule selected from the group consisting of:
a) a nucleic acid molecule comprising a nucleotide sequence which is at least 60% identical to the nucleotide sequence of SEQ ID NO:1 or SEQ ID NO:3, wherein said sequence encodes a polypeptide having biological activity; b) a nucleic acid molecule comprising a fragment of at least 20 nucleotides of the nucleotide sequence of SEQ ID NO:1 or SEQ ID NO:3; c) a nucleic acid molecule which encodes a polypeptide comprising the amino acid sequence of SEQ ID NO:2; d) a nucleic acid molecule which encodes a fragment of a polypeptide comprising the amino acid sequence of SEQ ID NO:2, wherein the fragment comprises at least 15 contiguous amino acids of SEQ ID NO:2; e) a nucleic acid molecule which encodes a naturally occurring allelic variant of a biologically active polypeptide comprising the amino acid sequence of SEQ ID NO:2, wherein the nucleic acid molecule hybridizes to a nucleic acid molecule comprising the complement of SEQ ID NO:1 or SEQ ID NO:3 under stringent conditions; and, f) a nucleic acid molecule comprising the complement of a), b), c), d), or e).
2 . The isolated nucleic acid molecule of claim 1 , which is selected from the group consisting of:
a) a nucleic acid comprising the nucleotide sequence of SEQ ID NO:1, SEQ ID NO:3, or complement thereof; and, b) a nucleic acid molecule which encodes a polypeptide comprising the amino acid sequence of SEQ ID NO:2.
3 . The nucleic acid molecule of claim 1 further comprising vector nucleic acid sequences.
4 . The nucleic acid molecule of claim 1 further comprising nucleic acid sequences encoding a heterologous polypeptide.
5 . A host cell which contains the nucleic acid molecule of claim 1 .
6 . The host cell of claim 5 which is a mammalian host cell.
7 . A non-human mammalian host cell containing the nucleic acid molecule of claim 1 .
8 . An isolated polypeptide selected from the group consisting of:
a) a biologically active polypeptide which is encoded by a nucleic acid molecule comprising a nucleotide sequence which is at least 60% identical to a nucleic acid comprising the nucleotide sequence of SEQ ID NO:1 or SEQ ID NO:3; b) a naturally occurring allelic variant of a biologically active polypeptide comprising the amino acid sequence of SEQ ID NO:2, wherein the polypeptide is encoded by a nucleic acid molecule which hybridizes to a nucleic acid molecule comprising the complement of SEQ ID NO:1 or SEQ ID NO:3 under stringent conditions; and, c) a fragment of a polypeptide comprising the amino acid sequence of SEQ ID NO:2, wherein the fragment comprises at least 15 contiguous amino acids of SEQ ID NO:2; and, d) a biologically active polypeptide having at least 60% sequence identity to the amino acid sequence SEQ ID NO:2.
9 . The isolated polypeptide of claim 8 comprising the amino acid sequence of SEQ ID NO:2.
10 . The polypeptide of claim 8 further comprising heterologous amino acid sequences.
11 . An antibody which selectively binds to a polypeptide of claim 8 .
12 . A method for producing a polypeptide selected from the group consisting of:
a) a polypeptide comprising the amino acid sequence of SEQ ID NO:2; b) a polypeptide comprising a fragment of the amino acid sequence of SEQ ID NO:2, wherein the fragment comprises at least 15 contiguous amino acids of SEQ ID NO:2; c) a naturally occurring allelic variant of a biologically active polypeptide comprising the amino acid sequence of SEQ ID NO:2, wherein the polypeptide is encoded by a nucleic acid molecule which hybridizes to a nucleic acid molecule comprising the complement of SEQ ID NO:1 or 3; and, d) a biologically active polypeptide having at least 60% sequence identity to the nucleic acid sequence of SEQ ID NO:2; comprising culturing a host cell under conditions in which the nucleic acid molecule is expressed.
13 . A method for detecting the presence of a polypeptide of claim 8 in a sample, comprising:
a) contacting the sample with a compound which selectively binds to a polypeptide of claim 8; and
b) determining whether the compound binds to the polypeptide in the sample.
14 . The method of claim 13 , wherein said sample is derived from a subject having or predisposed to cancer.
15 . The method of claim 13 , wherein the compound which binds to the polypeptide is an antibody.
16 . A kit comprising a compound which selectively binds to a polypeptide of claim 8 and instructions for use.
17 . A method for detecting the presence of a nucleic acid molecule of claim 1 in a sample, comprising the steps of:
a) contacting the sample with a nucleic acid probe or primer which selectively hybridizes to the nucleic acid molecule; and
b) determining whether the nucleic acid probe or primer binds to a nucleic acid molecule in the sample.
18 . The method of claim 17 , wherein said sample is derived from a subject having or predisposed to cancer.
19 . The method of claim 17 , wherein the sample comprises mRNA molecules and is contacted with a nucleic acid probe.
20 . A kit comprising a compound which selectively hybridizes to a nucleic acid molecule of claim 1 and instructions for use.
21 . A method for identifying a compound which binds to a polypeptide of claim 8 comprising the steps of:
a) contacting a polypeptide, or a cell expressing a polypeptide of claim 8 with a test compound; and
b) determining whether the polypeptide binds to the test compound.
22 . The method of claim 21 , wherein the binding of the test compound to the polypeptide is detected by a method selected from the group consisting of:
a) detection of binding by direct detecting of test compound/polypeptide binding; b) detection of binding using a competition binding assay; c) detection of binding using an assay for cytidine deaminase-like mediated activity.
23 . A method for identifying a compound which modulates the activity of a polypeptide of claim 8 , comprising:
a) contacting a polypeptide of claim 8 with a test compound; and b) determining the effect of the test compound on the activity of the polypeptide to thereby identify a compound that modulates the activity of the polypeptide.
24 . A method for modulating the level or activity of a nucleic acid molecule of claim 1 , said method comprising contacting said nucleic acid molecule with an agent under conditions that allow the agent to modulate the level or activity of the nucleic acid molecule.
25 . The method of claim 24 , wherein said host cell is in a subject having or predisposed to cancer.
26 . A method for modulating the level or activity of a polypeptide of claim 8 comprising contacting a polypeptide or a cell expressing a polypeptide of claim 8 with a compound which binds to the polypeptide in a sufficient concentration to modulate the activity of the polypeptide.
27 . The method of claim 26 , wherein said modulation is in a subject having or predisposed to cancer.
28 . A method for detecting a propensity of a subject to develop cancer, said method comprising obtaining a sample from said subject and contacting said sample with an agent that specifically allows detection of the presence of a nucleic acid molecule of claim 1 in the sample and then detecting the presence of the nucleic acid molecule.Join the waitlist — get patent alerts
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