Genome-wide analysis of estrogen receptor binding sites

被引:1041
作者
Carroll, Jason S.
Meyer, Clifford A.
Song, Jun
Li, Wei
Geistlinger, Timothy R.
Eeckhoute, Jerome
Brodsky, Alexander S.
Keeton, Erika Krasnickas
Fertuck, Kirsten C.
Hall, Giles F.
Wang, Qianben
Bekiranov, Stefan
Sementchenko, Victor
Fox, Edward A.
Silver, Pamela A.
Gingeras, Thomas R.
Liu, X. Shirley
Brown, Myles
机构
[1] Harvard Univ, Sch Med, Dept Med Oncol, Dana Farber Canc Inst, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Dept Biostat & Computat Biol, Dana Farber Canc Inst, Boston, MA 02115 USA
[3] Harvard Univ, Sch Publ Hlth, Boston, MA 02115 USA
[4] Brown Univ, Labs Mol Med, Ctr Genom & Proteom, Providence, RI 02903 USA
[5] Harvard Univ, Sch Med, Dept Canc Biol, Dana Farber Canc Inst, Boston, MA 02115 USA
[6] Affymetrix, Santa Clara, CA 95051 USA
[7] Harvard Univ, Sch Med, Dept Syst Biol, Boston, MA 02115 USA
关键词
D O I
10.1038/ng1901
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
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.
引用
收藏
页码:1289 / 1297
页数:9
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