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Enhancer of Rudimentary Cooperates with Conserved RNA-Processing Factors to Promote Meiotic mRNA Decay and Facultative Heterochromatin Assembly

机译:基本的增强子与保守的RNA加工因子配合,促进减数分裂mRNA衰变和兼性异染色质组装。

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摘要

Erh1, the fission yeast homolog of Enhancer of rudimentary, is implicated in meiotic mRNA elimination during vegetative growth, but its function is poorly understood. We show that Erh1 and the RNA-binding protein Mmi1 form a stoichiometric complex, called the Erh1-Mmi1 complex (EMC), to promote meiotic mRNA decay and facultative heterochromatin assembly. To perform these functions, EMC associates with two distinct complexes, Mtl1-Red1 core (MTREC) and CCR4-NOT. Whereas MTREC facilitates assembly of heterochromatin islands coating meiotic genes silenced by the nuclear exosome, CCR4-NOT promotes RNAi-dependent heterochromatin domain (HOOD) formation at EMC-target loci. CCR4-NOT also assembles HOODs at retrotransposons and regulated genes containing cryptic introns. We find that CCR4-NOT facilitates HOOD assembly through its association with the conserved Pir2/ARS2 protein, and also maintains rDNA integrity and silencing by promoting heterochromatin formation. Our results reveal connections among Erh1, CCR4-NOT, Pir2/ARS2, and RNAi, which target heterochromatin to regulate gene expression and protect genome integrity.
机译:Erh1是最基本的增强子的裂变酵母同源物,与营养生长过程中减数分裂mRNA的消除有关,但其功能尚不清楚。我们显示Erh1和RNA结合蛋白Mmi1形成化学计量的复杂,称为Erh1-Mmi1复杂(EMC),以促进减数分裂mRNA衰变和兼性异染色质组装。为了执行这些功能,EMC与两个不同的复合体(Mtl1-Red1核心(MTREC)和CCR4-NOT)相关联。尽管MTREC促进了被核外体沉默的包被减数分裂基因的异染色质岛的组装,但CCR4-NOT促进了EMC靶基因位点上依赖RNAi的异染色质域(HOOD)的形成。 CCR4-NOT还在逆转座子和含有隐含内含子的调控基因上组装HOOD。我们发现,CCR4-NOT通过与保守的Pir2 / ARS2蛋白缔合而促进HOOD装配,并通过促进异染色质形成来维持rDNA完整性和沉默。我们的研究结果揭示了Erh1,CCR4-NOT,Pir2 / ARS2和RNAi之间的联系,后者靶向异染色质以调节基因表达并保护基因组完整性。

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