Wellcome Trust Centre for Cell Biology and Institute of Cell Biology, School of Biological Sciences, The University of Edinburgh, Edinburgh EH9 3JR, Scotland, UK.
Cell. 2010 Mar 5;140(5):666-77. doi: 10.1016/j.cell.2010.01.038.
In fission yeast, RNAi directs heterochromatin formation at centromeres, telomeres, and the mating type locus. Noncoding RNAs transcribed from repeat elements generate siRNAs that are incorporated into the Argonaute-containing RITS complex and direct it to nascent homologous transcripts. This leads to recruitment of the CLRC complex, including the histone methyltransferase Clr4, promoting H3K9 methylation and heterochromatin formation. A key question is what mediates the recruitment of Clr4/CLRC to transcript-bound RITS. We have identified a LIM domain protein, Stc1, that is required for centromeric heterochromatin integrity. Our analyses show that Stc1 is specifically required to establish H3K9 methylation via RNAi, and interacts both with the RNAi effector Ago1, and with the chromatin-modifying CLRC complex. Moreover, tethering Stc1 to a euchromatic locus is sufficient to induce silencing and heterochromatin formation independently of RNAi. We conclude that Stc1 associates with RITS on centromeric transcripts and recruits CLRC, thereby coupling RNAi to chromatin modification.
在裂殖酵母中,RNAi 指导着着丝粒、端粒和交配型基因座的异染色质形成。由重复元件转录的非编码 RNA 产生 siRNA,这些 siRNA 被整合到包含 Argonaute 的 RITS 复合物中,并指导其与新生的同源转录本结合。这导致 CLRC 复合物的募集,包括组蛋白甲基转移酶 Clr4,促进 H3K9 甲基化和异染色质形成。一个关键问题是,是什么介导了 Clr4/CLRC 与转录结合的 RITS 的募集。我们已经鉴定出一种 LIM 结构域蛋白 Stc1,它是着丝粒异染色质完整性所必需的。我们的分析表明,Stc1 是通过 RNAi 特异性地建立 H3K9 甲基化所必需的,并且与 RNAi 效应因子 Ago1 以及染色质修饰的 CLRC 复合物相互作用。此外,将 Stc1 锚定到常染色质区域足以独立于 RNAi 诱导沉默和异染色质形成。我们得出结论,Stc1 与着丝粒转录本上的 RITS 结合,并募集 CLRC,从而将 RNAi 与染色质修饰联系起来。