作者: D Cobrinik , P Whyte , D S Peeper , T Jacks , R A Weinberg
关键词: GTPase-activating protein 、 Cell Cycle Protein 、 DNA-binding protein 、 E2F 、 Nuclear protein 、 Biology 、 Retinoblastoma protein 、 Binding protein 、 Molecular biology 、 Retinoblastoma-Like Protein p107
摘要: Association of the E2F transcription factor with pRb and p107 proteins appears to regulate activity and, in turn, affect cell cycle progression. We found, however, that are only minor E2F-associated G0/G1 mouse fibroblasts, we sought identify major partner protein these cells. Because adenovirus E1A oncoprotein seemed able bind G0 partner, enriched for associated both an E2F-binding site DNA column E1A. The species early G1 fibroblasts detected this approach had properties identical pRb- p107-related p130 protein. In serum-stimulated cells, replaced as near G1/S border, concomitant increase levels. p130-E2F complexes resembled p107-E2F their ability cyclin-cdk kinases, they appeared be cyclin E-cdk2 kinase late These observations indicate factors regulated by a succession which associate during defined stages cycle.