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SMC装载蛋白Scc2促进非编码RNA生物合成及翻译保真度。

The SMC Loader Scc2 Promotes ncRNA Biogenesis and Translational Fidelity.

作者信息

Zakari Musinu, Trimble Ross Rhonda, Peak Allison, Blanchette Marco, Seidel Chris, Gerton Jennifer L

机构信息

Stowers Institute for Medical Research, Kansas City, Missouri, United States of America; Universite Pierre et Marie Curie (Paris VI), Paris, France.

Stowers Institute for Medical Research, Kansas City, Missouri, United States of America.

出版信息

PLoS Genet. 2015 Jul 15;11(7):e1005308. doi: 10.1371/journal.pgen.1005308. eCollection 2015 Jul.

Abstract

The Scc2-Scc4 complex is essential for loading the cohesin complex onto DNA. Cohesin has important roles in chromosome segregation, DSB repair, and chromosome condensation. Here we report that Scc2 is important for gene expression in budding yeast. Scc2 and the transcriptional regulator Paf1 collaborate to promote the production of Box H/ACA snoRNAs which guide pseudouridylation of RNAs including ribosomal RNA. Mutation of SCC2 was associated with defects in the production of ribosomal RNA, ribosome assembly, and splicing. While the scc2 mutant does not have a general defect in protein synthesis, it shows increased frameshifting and reduced cap-independent translation. These findings suggest Scc2 normally promotes a gene expression program that supports translational fidelity. We hypothesize that translational dysfunction may contribute to the human disorder Cornelia de Lange syndrome, which is caused by mutations in NIPBL, the human ortholog of SCC2.

摘要

Scc2-Scc4复合物对于将黏连蛋白复合物加载到DNA上至关重要。黏连蛋白在染色体分离、双链断裂修复和染色体凝聚中发挥重要作用。在此我们报告,Scc2在芽殖酵母的基因表达中很重要。Scc2与转录调节因子Paf1协作,促进Box H/ACA小核仁RNA的产生,这些小核仁RNA指导包括核糖体RNA在内的RNA的假尿嘧啶化。SCC2的突变与核糖体RNA产生、核糖体组装和剪接缺陷有关。虽然scc2突变体在蛋白质合成方面没有普遍缺陷,但它表现出移码增加和非帽依赖性翻译减少。这些发现表明,Scc2通常促进支持翻译保真度的基因表达程序。我们推测,翻译功能障碍可能导致人类疾病科妮莉亚·德朗热综合征,该综合征由SCC2的人类直系同源基因NIPBL的突变引起。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b91/4503661/9d83a1309f44/pgen.1005308.g001.jpg

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