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首页> 外文期刊>Genes and Development: a Journal Devoted to the Molecular Analysis of Gene Expression in Eukaryotes, Prokaryotes, and Viruses >A conserved ncrna-binding protein recruits silencing factors to heterochromatin through an RNAi-independent mechanism
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A conserved ncrna-binding protein recruits silencing factors to heterochromatin through an RNAi-independent mechanism

机译:保守的ncrna结合蛋白通过RNAi独立机制将沉默因子募集到异染色质

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摘要

Long noncoding RNAs (lncRNAs) can trigger repressive chromatin, but how they recruit silencing factors remains unclear. In Schizosaccharomyces pombe, heterochromatin assembly on transcribed noncoding pericentromeric repeats requires both RNAi and RNAi-independent mechanisms. In Saccharomyces cerevisiae, which lacks a repressive chromatin mark (H3K9me [methylated Lys9 on histone H3]), unstable ncRNAs are recognized by the RNA-binding protein Nrd1. We show that the S. pombe ortholog Seb1 is associated with pericentromeric lncRNAs. Individual mutation of dcr1+ (Dicer) or seb1+ results in equivalent partial reductions of pericentromeric H3K9me levels, but a double mutation eliminates this mark. Seb1 functions independently of RNAi by recruiting the NuRD (nucleosome remodeling and deacetylase)-related chromatin-modifying complex SHREC (Snf2-HDAC [histone deacetylase] repressor complex).
机译:较长的非编码RNA(lncRNA)可以触发抑制性染色质,但如何募集沉默因子仍不清楚。在粟酒裂殖酵母中,转录的非编码周边着丝粒重复序列上的异染色质组装需要RNAi和RNAi独立机制。在缺乏抑制性染色质标记(H3K9me [组蛋白H3上的甲基化Lys9])的酿酒酵母中,不稳定的ncRNA被RNA结合蛋白Nrd1识别。我们显示,S。pombe直系同源物Seb1与着丝粒lncRNAs相关。 dcr1 +(Dicer)或seb1 +的个别突变会导致percentromeric H3K9me水平的部分降低,但是双重突变消除了这一标记。 Seb1通过募集与NuRD(核小体重塑和脱乙酰基酶)相关的染色质修饰复合物SHREC(Snf2-HDAC [组蛋白脱乙酰基酶]阻遏物复合体)而独立于RNAi发挥作用。

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