CBP/p300 histone acetyl-transferase activity is important for the G1/S transition

被引:116
作者
Ait-Si-Ali, S
Polesskaya, A
Filleur, S
Ferreira, R
Duquet, A
Robin, P
Vervish, A
Trouche, D
Cabon, F
Harel-Bellan, A
机构
[1] CNRS, IFC 01, Lab Oncogenese Differenciat & Transduct Signal, F-94801 Villejuif, France
[2] CNRS, IFC 01, Lab Cytoretrie, F-94801 Villejuif, France
[3] CNRS, UPR 9006, LBME, F-31062 Toulouse, France
关键词
CBP/p300; histone acetyl-transferase; proliferation; E2F; G1/S transition; microinjection;
D O I
10.1038/sj.onc.1203562
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:2430 / 2437
页数:8
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