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RNA监测因子UPF1通过其E3泛素连接酶活性抑制肌生成。

The RNA Surveillance Factor UPF1 Represses Myogenesis via Its E3 Ubiquitin Ligase Activity.

作者信息

Feng Qing, Jagannathan Sujatha, Bradley Robert K

机构信息

Computational Biology Program, Public Health Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA; Basic Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA; Molecular and Cellular Biology Graduate Program, University of Washington, Seattle, WA 98105, USA.

Computational Biology Program, Public Health Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA; Basic Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA; Human Biology Division, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA.

出版信息

Mol Cell. 2017 Jul 20;67(2):239-251.e6. doi: 10.1016/j.molcel.2017.05.034. Epub 2017 Jun 29.

DOI:10.1016/j.molcel.2017.05.034
PMID:28669802
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5536975/
Abstract

UPF1 is an RNA helicase that orchestrates nonsense-mediated decay and other RNA surveillance pathways. While UPF1 is best known for its basal cytoprotective role in degrading aberrant RNAs, UPF1 also degrades specific, normally occurring mRNAs to regulate diverse cellular processes. Here we describe a role for UPF1 in regulated protein decay, wherein UPF1 acts as an E3 ubiquitin ligase to repress human skeletal muscle differentiation. Suppressing UPF1 accelerates myogenesis, while ectopically increasing UPF1 levels slows myogenesis. UPF1 promotes the decay of MYOD protein, a transcription factor that is a master regulator of myogenesis, while leaving MYOD mRNA stability unaffected. UPF1 acts as an E3 ligase via its RING domain to promote MYOD protein ubiquitination and degradation. Our data characterize a regulatory role for UPF1 in myogenesis, and they demonstrate that UPF1 provides a mechanistic link between the RNA and protein decay machineries in human cells.

摘要

UPF1是一种RNA解旋酶,它协调无义介导的衰变和其他RNA监测途径。虽然UPF1因其在降解异常RNA中的基础细胞保护作用而最为人所知,但UPF1也会降解特定的、正常存在的mRNA以调节多种细胞过程。在这里,我们描述了UPF1在调节蛋白质衰变中的作用,其中UPF1作为一种E3泛素连接酶来抑制人类骨骼肌分化。抑制UPF1可加速肌生成,而异位增加UPF1水平则会减缓肌生成。UPF1促进肌生成的主要调节因子——转录因子MYOD蛋白的衰变,同时不影响MYOD mRNA的稳定性。UPF1通过其RING结构域作为E3连接酶来促进MYOD蛋白的泛素化和降解。我们的数据表征了UPF1在肌生成中的调节作用,并且表明UPF1在人类细胞的RNA和蛋白质衰变机制之间提供了一种机制联系。

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SONAR Discovers RNA-Binding Proteins from Analysis of Large-Scale Protein-Protein Interactomes.声纳通过对大规模蛋白质-蛋白质相互作用组的分析发现RNA结合蛋白。
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