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Mbf1 ensures Polycomb silencing by protecting E(z) mRNA From degradation by Pacman

机译:MBF1通过保护Pacman的降解保护E(Z)mRNA来确保Polycomb沉默

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Under stress conditions, the coactivator Multiprotein bridging factor 1 (Mbf1) translocates from ttie cytoplasm into the nucleus to induce stress-response genes. However, its role in the cytoplasm, where it is mainly located, has remained elusive. Here, we show that Dmsophila Mbf1 associates with E(z) mRNA and protects it from degradation by the exoribonuclease Pacman (Pcm), thereby ensuring Polycomb silencing. In genetic studies, loss of mbf1 function enhanced a Polycomb phenotype in Polycomb group mutants, and was accompanied by a significant reduction in E(z) mRNA expression. Furthermore, a pcm mutation suppressed the Polycomb phenotype and restored the expression level of E(z) mRNA, while pcm overexpression exhibited the Polycomb phenotype in the mbf1 mutant but not in the wild-type background. In vitro, Mbf1 protected E(z) RNA from Pcm activity. Our results suggest that Mbfl buffers fluctuations in Pcm activity to maintain an E(z) mRNA expression level sufficient for Polycomb silencing.
机译:在应力条件下,将共酰胺多蛋白桥接因子1(MBF1)从TTIE细胞质转移到细胞核中以诱导应激反应基因。然而,它在主要位于细胞质中的作用仍然难以捉摸。在这里,我们表明DMSOPHILA MBF1与E(Z)mRNA相关联,并保护其免受Exoribonuclease Pacman(PCM)的降解,从而确保了PolycomB沉默。在遗传研究中,MBF1功能的丧失增强了多元组突变体中的多元酶表型,并伴随着E(Z)mRNA表达的显着降低。此外,PCM突变抑制了Polycomb表型并恢复了E(Z)mRNA的表达水平,而PCM过表达在MBF1突变体中表现出polycomb表型,但不在野生型背景中表现出polycomb表型。体外,来自PCM活性的MBF1保护e(Z)RNA。我们的研究结果表明,MBFL缓冲液在PCM活性中波动,以维持足以用于Polycomb沉默的E(Z)mRNA表达水平。

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