Ciferri Claudio, Lander Gabriel C, Maiolica Alessio, Herzog Franz, Aebersold Ruedi, Nogales Eva
Department of Molecular and Cell Biology , University of California , Berkeley , United States.
Elife. 2012 Oct 30;1:e00005. doi: 10.7554/eLife.00005.
Polycomb Repressive Complex 2 (PRC2) is essential for gene silencing, establishing transcriptional repression of specific genes by tri-methylating Lysine 27 of histone H3, a process mediated by cofactors such as AEBP2. In spite of its biological importance, little is known about PRC2 architecture and subunit organization. Here, we present the first three-dimensional electron microscopy structure of the human PRC2 complex bound to its cofactor AEBP2. Using a novel internal protein tagging-method, in combination with isotopic chemical cross-linking and mass spectrometry, we have localized all the PRC2 subunits and their functional domains and generated a detailed map of interactions. The position and stabilization effect of AEBP2 suggests an allosteric role of this cofactor in regulating gene silencing. Regions in PRC2 that interact with modified histone tails are localized near the methyltransferase site, suggesting a molecular mechanism for the chromatin-based regulation of PRC2 activity.DOI:http://dx.doi.org/10.7554/eLife.00005.001.
多梳抑制复合物2(PRC2)对于基因沉默至关重要,它通过对组蛋白H3的赖氨酸27进行三甲基化来建立特定基因的转录抑制,这一过程由AEBP2等辅助因子介导。尽管其具有生物学重要性,但人们对PRC2的结构和亚基组织了解甚少。在此,我们展示了与辅助因子AEBP2结合的人类PRC2复合物的首个三维电子显微镜结构。使用一种新型的内部蛋白质标记方法,结合同位素化学交联和质谱分析,我们确定了所有PRC2亚基及其功能结构域的位置,并生成了详细的相互作用图谱。AEBP2的位置和稳定作用表明该辅助因子在调节基因沉默中具有变构作用。PRC2中与修饰组蛋白尾巴相互作用的区域位于甲基转移酶位点附近,这提示了基于染色质调节PRC2活性的分子机制。DOI:http://dx.doi.org/10.7554/eLife.00005.001。