Transcriptional regulation and function during the human cell cycle

被引:356
作者
Cho, RJ
Huang, MX
Campbell, MJ
Dong, HL
Steinmetz, L
Sapinoso, L
Hampton, G
Elledge, SJ
Davis, RW
Lockhart, DJ
机构
[1] Stanford Univ, Sch Med, Dept Genet, Stanford, CA 94305 USA
[2] Baylor Coll Med, Howard Hughes Med Inst, Dept Biochem & Mol Biol, Dept Mol & Human Genet, Houston, TX 77030 USA
[3] Affymetrix Inc, Santa Clara, CA USA
[4] Stanford Univ, Sch Med, Dept Biochem, Stanford, CA USA
[5] Mol Applicat Grp, Palo Alto, CA USA
[6] Novartis Res Fdn, Genomics Inst, San Diego, CA USA
[7] Salk Inst Biol Studies, Genet Lab, La Jolla, CA 92037 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1038/83751
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
We report here the transcriptional profiling of the cell cycle on a genome-wide scale in human fibroblasts. We identified approximately 700 genes that display transcriptional fluctuation with a periodicity consistent with that of the cell cycle. Systematic analysis of these genes revealed functional organization within groups of coregulated transcripts. A diverse set of cytoskeletal reorganization genes exhibit cell-cycle-dependent regulation, indicating that biological pathways are redirected for the execution of cell division. Many genes involved in cell motility and remodeling of the extracellular matrix are expressed predominantly in M phase, indicating a mechanism for balancing proliferative and invasive cellular behavior. Transcripts upregulated during S phase displayed extensive overlap with genes induced by DNA damage; cell-cycle-regulated transcripts may therefore constitute coherent programs used in response to external stimuli. Our data also provide clues to biological function for hundreds of previously uncharacterized human genes.
引用
收藏
页码:48 / 54
页数:7
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