| Literature DB >> 10828885 |
S Ait-Si-Ali1, A Polesskaya, S Filleur, R Ferreira, A Duquet, P Robin, A Vervish, D Trouche, F Cabon, A Harel-Bellan.
Abstract
Transforming viral proteins such as E1A which force quiescent cells into S phase have two essential cellular target proteins, Rb and CBP/p300. Rb regulates the G1/S transition by controlling the transcription factor E2F. CBP/p300 is a transcriptional co-activator with intrinsic histone acetyl-transferase activity. This activity is regulated in a cell cycle dependent manner and shows a peak at the G1/S transition, suggesting a function for CBP/p300 in this crucial step of the cell cycle. Here, we have artificially modulated CBP/p300 levels in individual cells through microinjection of specific antibodies and expression vectors. We show that CBP/p300 is required for cell proliferation and has an essential function during the G1/S transition. Using the same microinjection system and GFP-reporter vectors, we demonstrate that CBP/p300 is essential for the activity of E2F, a transcription factor that controls the G1/S transition. In addition, our results suggest that CBP HAT activity is required both for the G1/S transition and for E2F activity. Thus CBP/p300 seems to be a versatile protein involved in opposing cellular processes, which raises the question of how its multiple activities are regulated.Entities:
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Year: 2000 PMID: 10828885 DOI: 10.1038/sj.onc.1203562
Source DB: PubMed Journal: Oncogene ISSN: 0950-9232 Impact factor: 9.867