Howard Hughes Medical Institute, Department of Molecular and Cell Biology, University of California, Berkeley, CA 94720, USA.
Trends Cell Biol. 2012 Jun;22(6):292-8. doi: 10.1016/j.tcb.2012.04.002. Epub 2012 May 7.
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 pre-existing 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.
胚胎干细胞(ES 细胞)与所有细胞类型一样,由其独特的转录特征定义。ES 细胞自我更新或退出多能状态并进入分化状态的能力需要其转录组和表观基因组发生广泛变化。值得注意的是,每个细胞命运的转录程序必须保持足够的可塑性,以便只有少数转录激活因子的表达可以通过与一系列意想不到的复杂共激活因子合作来克服先前的状态,从而指定、限制和稳定新的状态。在这里,我们讨论了我们对共激活因子如何解释不同激活因子编码的多条信息以及将来自不同调节剂的信号整合到干细胞特异性转录输出中的理解的最新进展。