Ezhkova Elena, Pasolli H Amalia, Parker Joel S, Stokes Nicole, Su I-hsin, Hannon Gregory, Tarakhovsky Alexander, Fuchs Elaine
Howard Hughes Medical Institute, Laboratory of Mammalian Cell Biology and Development, The Rockefeller University, New York, NY 10065, USA.
Cell. 2009 Mar 20;136(6):1122-35. doi: 10.1016/j.cell.2008.12.043.
Although in vitro studies of embryonic stem cells have identified polycomb repressor complexes (PRCs) as key regulators of differentiation, it remains unclear as to how PRC-mediated mechanisms control fates of multipotent progenitors in developing tissues. Here, we show that an essential PRC component, Ezh2, is expressed in epidermal progenitors but diminishes concomitant with embryonic differentiation and with postnatal decline in proliferative activity. We show that Ezh2 controls proliferative potential of basal progenitors by repressing the Ink4A-Ink4B locus and tempers the developmental rate of differentiation by preventing premature recruitment of AP1 transcriptional activator to the structural genes that are required for epidermal differentiation. Together, our studies reveal that PRCs control epigenetic modifications temporally and spatially in tissue-restricted stem cells. They maintain their proliferative potential and globally repressing undesirable differentiation programs while selectively establishing a specific terminal differentiation program in a stepwise fashion.
尽管对胚胎干细胞的体外研究已将多梳抑制复合物(PRCs)确定为分化的关键调节因子,但PRC介导的机制如何控制发育组织中多能祖细胞的命运仍不清楚。在这里,我们表明,PRC的一个重要组成部分Ezh2在表皮祖细胞中表达,但随着胚胎分化以及出生后增殖活性的下降而减少。我们表明,Ezh2通过抑制Ink4A-Ink4B基因座来控制基底祖细胞的增殖潜能,并通过防止AP1转录激活因子过早募集到表皮分化所需的结构基因来调节分化的发育速率。总之,我们的研究表明,PRCs在组织限制性干细胞中在时间和空间上控制表观遗传修饰。它们维持其增殖潜能并全局抑制不良分化程序,同时以逐步方式选择性地建立特定的终末分化程序。