Department of Molecular Biology and Biochemistry, Wesleyan University, Middletown, Connecticut, USA.
Mol Cell Biol. 2012 Jul;32(14):2784-93. doi: 10.1128/MCB.06399-11. Epub 2012 May 14.
Epigenetic mechanisms maintain the specific characteristics of differentiated cells by ensuring the inheritance of gene expression patterns through DNA replication and mitosis. We examined the mechanism of epigenetic inheritance of Sir protein-dependent transcriptional silencing in Saccharomyces cerevisiae by examining gene expression and molecular markers of silencing at the silent mating type loci under conditions of limiting Sir3 protein. We observed that silencing at HMR, as previously reported for HML, is epigenetically inherited. This inheritance is accompanied by an increased ability of previously silenced cells to retain or recruit limiting Sir3 protein to cis-acting silencer sequences. We also observed that the low H4-K16 histone acetylation and H3-K79 methylation associated with a silenced HMR locus persist in recently derepressed cells for several generations at levels of Sir3 insufficient to maintain these marks in long-term-derepressed cells. The unique ability of previously silenced cells to retain Sir3 protein, maintain silencing-specific histone modifications, and repress HMR transcription at levels of Sir3 insufficient to mediate these effects in long-term-derepressed cells suggests that a cis-acting, chromatin-based mechanism drives epigenetic inheritance at this locus.
表观遗传机制通过确保基因表达模式在 DNA 复制和有丝分裂过程中的遗传,维持分化细胞的特定特征。我们通过检查限制 Sir3 蛋白条件下沉默交配型基因座的基因表达和沉默的分子标记,研究了酵母中 Sir 蛋白依赖性转录沉默的表观遗传遗传机制。我们观察到,正如先前在 HML 中报道的那样,HMR 的沉默是通过表观遗传方式遗传的。这种遗传伴随着先前沉默的细胞保留或招募限制的 Sir3 蛋白到顺式作用沉默序列的能力增强。我们还观察到,与沉默的 HMR 基因座相关的低 H4-K16 组蛋白乙酰化和 H3-K79 甲基化在最近去抑制的细胞中持续存在数代,其 Sir3 水平不足以在长期去抑制的细胞中维持这些标记。先前沉默的细胞保留 Sir3 蛋白、维持沉默特异性组蛋白修饰以及抑制 HMR 转录的独特能力,其 Sir3 水平不足以介导长期去抑制细胞中的这些效应,这表明顺式作用、基于染色质的机制驱动了该基因座的表观遗传遗传。