Genome-wide analysis of estrogen receptor binding sites

被引:0
|
作者
Jason S Carroll
Clifford A Meyer
Jun Song
Wei Li
Timothy R Geistlinger
Jérôme Eeckhoute
Alexander S Brodsky
Erika Krasnickas Keeton
Kirsten C Fertuck
Giles F Hall
Qianben Wang
Stefan Bekiranov
Victor Sementchenko
Edward A Fox
Pamela A Silver
Thomas R Gingeras
X Shirley Liu
Myles Brown
机构
[1] Dana-Farber Cancer Institute,Department of Medical Oncology
[2] Harvard Medical School,Department of Biostatistics and Computational Biology
[3] Dana-Farber Cancer Institute,Department of Cancer Biology
[4] Harvard Medical School,Department of Systems Biology
[5] Harvard School of Public Health,Department of Biochemistry and Molecular Genetics
[6] Brown University,undefined
[7] Laboratories for Molecular Medicine,undefined
[8] Center for Genomics and Proteomics,undefined
[9] Dana-Farber Cancer Institute,undefined
[10] Harvard Medical School,undefined
[11] Affymetrix,undefined
[12] 3380 Central Expressway,undefined
[13] Harvard Medical School,undefined
[14] University of Virginia School of Medicine,undefined
来源
Nature Genetics | 2006年 / 38卷
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摘要
The estrogen receptor is the master transcriptional regulator of breast cancer phenotype and the archetype of a molecular therapeutic target. We mapped all estrogen receptor and RNA polymerase II binding sites on a genome-wide scale, identifying the authentic cis binding sites and target genes, in breast cancer cells. Combining this unique resource with gene expression data demonstrates distinct temporal mechanisms of estrogen-mediated gene regulation, particularly in the case of estrogen-suppressed genes. Furthermore, this resource has allowed the identification of cis-regulatory sites in previously unexplored regions of the genome and the cooperating transcription factors underlying estrogen signaling in breast cancer.
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页码:1289 / 1297
页数:8
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