Cell-cycle regulatory proteins, and uses related thereto
AssigneeCold Spring Harbor
InventorsDavid H. Beach, Manuel Serrano, Gregory J. Hannon
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AssigneeCold Spring Harbor
InventorsDavid H. Beach, Manuel Serrano, Gregory J. Hannon
Estimating the term…
The present invention relates to the discovery in eukaryotic cells, particularly mammalian cells, of a novel family of cell-cycle regulatory proteins (“CCR-proteins”). As described herein, this family of proteins includes a polypeptide having an apparent molecular weight of 16 kDa, and a polypeptide having an apparent molecular weight of approximately 15 kDa, each of which can function as an inhibitor of cell-cycle progression, and therefore ultimately of cell growth. Thus, similar to the role of p21 to the p53 checkpoint, the subject CCR-proteins may function coordinately with the cell-cycle regulatory protein, retinoblastoma (RB). Furthermore, the CCR-protein family includes a protein having an apparent molecular weight of 13.5 kDa (hereinafter “p13.5”). The presumptive role of p13.5, like p16 and p15, is in the regulation of the cell-cycle.
A substantially pure preparation of a cell-cycle regulatory (CCR) protein, or a fragment thereof, which specifically binds to a cyclin-dependent kinase (CDK), which CCR protein is encoded by a nucleic acid sequence which hybridizes under stringent conditions, including a wash step of 2×SSC at 50° C., to the nucleic acid sequence of SEQ ID No:
An isolated polypeptide comprising a CCR-protein encoded by a nucleic acid which hybridizes under stringent conditions, including a wash step of 2×SSC at 50° C., or higher stringency to a nucleic acid sequence of SEQ ID No:
A substantially pure preparation of a polypeptide of SEQ ID No. 2, which polypeptide specifically interacts with cyclin-dependent kinase 4 (CDK4), which specific interaction is affected by residues Lys-22, Arg-24, His-95 and Asp-97 of CDK4.
Dependencies are inferred from the claim text.