Transcriptional regulation by coactivators in embryonic stem cells
被引:22
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作者:
Fong, Yick W.
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Univ Calif Berkeley, Dept Mol & Cell Biol, Howard Hughes Med Inst, Berkeley, CA 94720 USAUniv Calif Berkeley, Dept Mol & Cell Biol, Howard Hughes Med Inst, Berkeley, CA 94720 USA
Fong, Yick W.
[1
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Cattoglio, Claudia
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Univ Calif Berkeley, Dept Mol & Cell Biol, Howard Hughes Med Inst, Berkeley, CA 94720 USAUniv Calif Berkeley, Dept Mol & Cell Biol, Howard Hughes Med Inst, Berkeley, CA 94720 USA
Cattoglio, Claudia
[1
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Yamaguchi, Teppei
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Univ Calif Berkeley, Dept Mol & Cell Biol, Howard Hughes Med Inst, Berkeley, CA 94720 USAUniv Calif Berkeley, Dept Mol & Cell Biol, Howard Hughes Med Inst, Berkeley, CA 94720 USA
Yamaguchi, Teppei
[1
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Tjian, Robert
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Univ Calif Berkeley, Dept Mol & Cell Biol, Howard Hughes Med Inst, Berkeley, CA 94720 USA
Univ Calif Berkeley, Li Ka Shing Ctr Biomed & Hlth Sci, Berkeley, CA 94720 USAUniv Calif Berkeley, Dept Mol & Cell Biol, Howard Hughes Med Inst, Berkeley, CA 94720 USA
Tjian, Robert
[1
,2
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机构:
[1] Univ Calif Berkeley, Dept Mol & Cell Biol, Howard Hughes Med Inst, Berkeley, CA 94720 USA
[2] Univ Calif Berkeley, Li Ka Shing Ctr Biomed & Hlth Sci, Berkeley, CA 94720 USA
Embryonic stem (ES) cells, like all cell types, are defined by their unique transcriptional signatures. The ability of ES cells to self-renew or exit the pluripotent state and enter differentiation requires extensive changes in their transcriptome and epigenome. Remarkably, transcriptional programs governing each cell fate must remain sufficiently malleable so that expression of only a handful of transcriptional activators can override the preexisting state by collaborating with an unexpectedly elaborate collection of coactivators to specify, restrict and stabilize the new state. Here, we discuss recent advances in our understanding of how the same coactivator can interpret multiple lines of information encoded by different activators and integrate signals from diverse regulators into stem cell-specific transcriptional outputs.
机构:
Newcastle Univ, Inst Human Genet, Newcastle Upon Tyne, Tyne & Wear, EnglandNewcastle Univ, Inst Human Genet, Newcastle Upon Tyne, Tyne & Wear, England
Atkinson, Stuart
Armstrong, Lyle
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Newcastle Univ, Inst Human Genet, Newcastle Upon Tyne, Tyne & Wear, EnglandNewcastle Univ, Inst Human Genet, Newcastle Upon Tyne, Tyne & Wear, England
机构:
Univ Calif San Francisco, Eli & Edythe Broad Ctr Regenerat Med & Stem Cell, San Francisco, CA 94143 USA
Univ Calif San Francisco, Ctr Reprod Sci, San Francisco, CA 94143 USA
Univ Calif San Francisco, Dept Urol, San Francisco, CA 94143 USAUniv Calif San Francisco, Eli & Edythe Broad Ctr Regenerat Med & Stem Cell, San Francisco, CA 94143 USA
Wang, Yangming
Blelloch, Robert
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机构:
Univ Calif San Francisco, Eli & Edythe Broad Ctr Regenerat Med & Stem Cell, San Francisco, CA 94143 USA
Univ Calif San Francisco, Ctr Reprod Sci, San Francisco, CA 94143 USA
Univ Calif San Francisco, Dept Urol, San Francisco, CA 94143 USAUniv Calif San Francisco, Eli & Edythe Broad Ctr Regenerat Med & Stem Cell, San Francisco, CA 94143 USA