The transcriptional foundation of pluripotency

被引:323
作者
Chambers, Ian [1 ]
Tomlinson, Simon R. [1 ]
机构
[1] Univ Edinburgh, MRC Ctr Regenerat Med, Inst Stem Cell Res, Sch Biol Sci, Edinburgh EH9 3JQ, Midlothian, Scotland
来源
DEVELOPMENT | 2009年 / 136卷 / 14期
基金
英国惠康基金; 英国医学研究理事会;
关键词
CELL SELF-RENEWAL; STEM-CELLS; REGULATORY CIRCUITRY; PROTEIN INTERACTIONS; DNA-BINDING; CRYSTAL-STRUCTURE; MOUSE EPIBLAST; ID PROTEINS; POU DOMAIN; NANOG;
D O I
10.1242/dev.024398
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
A fundamental goal in biology is to understand the molecular basis of cell identity. Pluripotent embryonic stem (ES) cell identity is governed by a set of transcription factors centred on the triumvirate of Oct4, Sox2 and Nanog. These proteins often bind to closely localised genomic sites. Recent studies have identified additional transcriptional modulators that bind to chromatin near sites occupied by Oct4, Sox2 and Nanog. This suggests that the combinatorial control of gene transcription might be fundamental to the ES cell state. Here we discuss how these observations advance our understanding of the transcription factor network that controls pluripotent identity and highlight unresolved issues that arise from these studies.
引用
收藏
页码:2311 / 2322
页数:12
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