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The cell cycle regulator p27Kip1 interacts with MCM7, a DNA replication licensing factor, to inhibit initiation of DNA replication
Authors:Nallamshetty Shriram  Crook Martin  Boehm Manfred  Yoshimoto Takanobu  Olive Michelle  Nabel Elizabeth G
Institution:National Heart, Lung, and Blood Institute, National Institutes of Health, Building 50, Room 4523, 50 Center Drive, Bethesda, MD 20892, USA.
Abstract:The G1/S phase restriction point is a critical checkpoint that interfaces between the cell cycle regulatory machinery and DNA replicator proteins. Here, we report a novel function for the cyclin-dependent kinase inhibitor p27Kip1 in inhibiting DNA replication through its interaction with MCM7, a DNA replication protein that is essential for initiation of DNA replication and maintenance of genomic integrity. We find that p27Kip1 binds the conserved minichromosome maintenance (MCM) domain of MCM7. The proteins interact endogenously in vivo in a growth factor-dependent manner, such that the carboxyl terminal domain of p27Kip1 inhibits DNA replication independent of its function as a cyclin-dependent kinase inhibitor. This novel function of p27Kip1 may prevent inappropriate initiation of DNA replication prior to S phase.
Keywords:β-gal  β-galactosidase  BSA  bovine serum albumin  CDK  cyclin-dependent kinase  CKI  cyclin-dependent kinase inhibitor  CS  consensus sequence  DM  deletion mutants  FBS  fetal bovine serum  MCM  minichromosome maintenance  NCBI  National Center for Biotechnology Information  NLS  nuclear localization signal  PAGE  polyacrylamide gel electrophoresis  WT  wild-type
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