Suppr超能文献

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.

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。

相似文献

6
Stau1 negatively regulates myogenic differentiation in C2C12 cells.Stau1对C2C12细胞的成肌分化起负向调节作用。
Genes Cells. 2008 Jun;13(6):583-92. doi: 10.1111/j.1365-2443.2008.01189.x. Epub 2008 Apr 17.

引用本文的文献

7
Translation-coupled mRNA quality control mechanisms.翻译偶联的mRNA质量控制机制。
EMBO J. 2023 Oct 4;42(19):e114378. doi: 10.15252/embj.2023114378. Epub 2023 Aug 22.
8
Coupled protein quality control during nonsense-mediated mRNA decay.NMD 过程中偶联的蛋白质量控制。
J Cell Sci. 2023 May 15;136(10). doi: 10.1242/jcs.261216. Epub 2023 May 23.

本文引用的文献

4
Ribosome-associated protein quality control.核糖体相关蛋白质量控制
Nat Struct Mol Biol. 2016 Jan;23(1):7-15. doi: 10.1038/nsmb.3147.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验