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Transcriptional regulation and function during the human cell cycle
被引:0
|作者:
Raymond J. Cho
Mingxia Huang
Michael J. Campbell
Helin Dong
Lars Steinmetz
Lisa Sapinoso
Garret Hampton
Stephen J. Elledge
Ronald W. Davis
David J. Lockhart
机构:
[1] Stanford University School of Medicine,Department of Genetics
[2] Howard Hughes Medical Institute,Department of Biochemistry and Molecular Biology, Department of Molecular and Human Genetics
[3] Baylor College of Medicine,Department of Biochemistry
[4] Molecular Applications Group,undefined
[5] Affymetrix,undefined
[6] Inc.,undefined
[7] Stanford University School of Medicine,undefined
[8] InGenuity Systems,undefined
[9] Inc.,undefined
[10] Celera Genomics,undefined
[11] Genomics Institute of the Novartis Research Foundation,undefined
[12] Salk Institute for Biological Studies,undefined
[13] Laboratory of Genetics,undefined
来源:
Nature Genetics
|
2001年
/
27卷
关键词:
D O I:
暂无
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学科分类号:
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.
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页码:48 / 54
页数:6
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