Control of cell cycle transcription during G1 and S phases

被引:1285
作者
Bertoli, Cosetta [1 ]
Skotheim, Jan M. [2 ]
de Bruin, Robertus A. M. [1 ]
机构
[1] UCL, Mol Cell Biol Lab, MRC, London WC1E 6BT, England
[2] Stanford Univ, Dept Biol, Stanford, CA 94305 USA
基金
美国国家卫生研究院; 英国医学研究理事会;
关键词
DNA-REPLICATION CHECKPOINT; E2F FAMILY-MEMBER; CDK-DEPENDENT PHOSPHORYLATION; RETINOBLASTOMA PROTEIN FAMILY; MULTISITE PHOSPHORYLATION; G1-SPECIFIC TRANSCRIPTION; SACCHAROMYCES-CEREVISIAE; DIFFERENTIAL REGULATION; G(1)-S TRANSCRIPTION; RESTRICTION POINT;
D O I
10.1038/nrm3629
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
The accurate transition from G1 phase of the cell cycle to S phase is crucial for the control of eukaryotic cell proliferation, and its misregulation promotes oncogenesis. During G1 phase, growth-dependent cyclin-dependent kinase (CDK) activity promotes DNA replication and initiates G1-to-S phase transition. CDK activation initiates a positive feedback loop that further increases CDK activity, and this commits the cell to division by inducing genome-wide transcriptional changes. G1-S transcripts encode proteins that regulate downstream cell cycle events. Recent work is beginning to reveal the complex molecular mechanisms that control the temporal order of transcriptional activation and inactivation, determine distinct functional subgroups of genes and link cell cycle-dependent transcription to DNA replication stress in yeast and mammals.
引用
收藏
页码:518 / 528
页数:11
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