A rapid, extensive, and transient transcriptional response to estrogen signaling in breast cancer cells.
A rapid, extensive, and transient transcriptional response to estrogen signaling in breast cancer cells.
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DOI:
10.1016/j.cell.2011.03.042
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发表时间:
2011-05-13
期刊:
影响因子:
64.5
通讯作者:
Kraus WL
中科院分区:
文献类型:
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作者:
Hah N;Danko CG;Core L;Waterfall JJ;Siepel A;Lis JT;Kraus WL
We report the immediate effects of estrogen signaling on the transcriptome of breast cancer cells using Global Run-On and sequencing (GRO-seq). The data were analyzed using a new bioinformatic approach that allowed us to identify transcripts directly from the GRO-seq data. We found that estrogen signaling directly regulates a strikingly large fraction of the transcriptome in a rapid, robust, and unexpectedly transient manner. In addition to protein coding genes, estrogen regulates the distribution and activity of all three RNA polymerases, and virtually every class of non-coding RNA that has been described to date. We also identified a large number of previously undetected estrogen-regulated intergenic transcripts, many of which are found proximal to estrogen receptor binding sites. Collectively, our results provide the most comprehensive measurement of the primary and immediate estrogen effects to date and a resource for understanding rapid signal-dependent transcription in other systems.
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