US2009210954A1PendingUtilityA1
Genes
Est. expiryJul 17, 2022(expired)· nominal 20-yr term from priority
A01K 2227/105A01K 67/0275A01K 2267/0306A01K 2217/075A01K 67/0276C07K 2319/60C12N 15/8509C07K 14/705A61P 35/00A61P 43/00A01K 2217/05
53
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Claims
Abstract
The present invention relates to two primordial germ cell-specific expressed genes, Fragilis and Stella . The sequences and sues of human Stella and Fragilis are disclosed herein, as are several mouse sequences related to Fragilis . The present invention relates to the use of Stella and Fragilis as markers for primordial germ cells and can be used to identify such cells. Additionally, the present invention relates to the use of Stella and Fragilis for the diagnosis, treatment and/or prevention of disease.
Claims
exact text as granted — not AI-modified1 - 17 . (canceled)
18 . A polypeptide comprising a human Stella amino acid sequence as shown in SEQ ID NO:4, or a sequence that is at least 95% identical thereto, wherein the polypeptide can serve as a marker of pluripotency.
19 . A polynucleotide sequence that codes for the polypeptide of claim 1 , suitable for use as a marker of pluripotency.
20 . The polynucleotide sequence of claim 19 , wherein the sequence is as shown in SEQ ID NO:3 or a sequence that is at least 95% identical thereto.
21 . A method for identifying a pluripotent cell comprising detecting expression of a Stella nucleic acid sequence in the cell.
22 . The method of claim 21 , wherein the nucleic acid sequence is as shown in SEQ ID NO:3 or a sequence that is at least 95% identical thereto.
23 . A method for identifying a pluripotent cell comprising detecting expression of a Stella polypeptide in the cell.
24 . The method of claim 23 , wherein the Stella polypeptide is as shown in SEQ ID NO:4, or a sequence that is at least 95% identical thereto.
25 . A polynucleotide expression construct suitable for detecting pluripotency in a cell, comprising:
i) at least the upstream sequences of a human Stella gene; and ii) the coding sequence of a reporter gene,
wherein expression of the coding sequence of the reporter gene is in operable combination with and under the control of the transcriptional control sequences of the human Stella gene, and
wherein induction of expression of the reporter gene in the cell can be detected and thereby correlated with a pluripotent phenotype in the cell.
26 . The polynucleotide expression construct of claim 25 , wherein the upstream sequences of the Stella gene include the 5′ untranslated region of the Stella gene.
27 . The polynucleotide expression construct of claim 25 , wherein the upstream sequences of the human Stella gene comprise up to about 8.5 kb of the nucleic acid sequence located upstream of the first exon of the human Stella coding sequence.
28 . The polynucleotide expression construct of claim 25 , wherein the expression construct is in the form of a transgene that can be integrated into the genome of the cell.
29 . The polynucleotide expression construct of claim 25 , wherein the cell is a stem cell.
30 . The polynucleotide expression construct of claim 25 , wherein the cell is selected from one of the group consisting of: a pluripotent cell; an embryonic stem cell; an embryonic germ cell; a germ cell tumour cell; and a primordial germ cell.
31 . The polynucleotide expression construct of claim 25 , wherein the cell is a human cell.
31 . The polynucleotide expression construct of claim 25 , wherein the reporter gene is a green fluorescent protein (GFP) gene.
32 . A cell comprising a polynucleotide expression construct of claim 25 .
33 . A non-human transgenic animal comprising a cell that comprises a polynucleotide expression construct of claim 25 .Join the waitlist — get patent alerts
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