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MRB10130 是一种 RESC 组装因子,可促进动质体 RNA 编辑的起始和延伸。

MRB10130 is a RESC assembly factor that promotes kinetoplastid RNA editing initiation and progression.

机构信息

Department of Microbiology and Immunology, University at Buffalo Jacobs School of Medicine and Biomedical Sciences, Buffalo, New York 14203, USA.

Department of Chemistry and Biochemistry, Kettering University, Flint, Michigan 48504, USA.

出版信息

RNA. 2019 Sep;25(9):1177-1191. doi: 10.1261/rna.071902.119. Epub 2019 Jun 20.

Abstract

Uridine insertion deletion editing in kinetoplastid protozoa requires a complex machinery, a primary component of which is the RNA editing substrate binding complex (RESC). RESC contains two modules termed GRBC (guide RNA binding complex) and REMC (RNA editing mediator complex), although how interactions between these modules and their mRNA and gRNA binding partners are controlled is not well understood. Here, we demonstrate that the ARM/HEAT repeat containing RESC protein, MRB10130, controls REMC association with mRNA- and gRNA-loaded GRBC. High-throughput sequencing analyses show that MRB10130 functions in both initiation and 3' to 5' progression of editing through gRNA-defined domains. Editing intermediates that accumulate upon MRB10130 depletion significantly intersect those in cells depleted of another RESC organizer, MRB7260, but are distinct from those in cells depleted of specific REMC proteins. We present a model in which MRB10130 coordinates numerous protein-protein and protein-RNA interactions during editing progression.

摘要

线粒体生物发生因子 10(TRMU)是线粒体型氨酰-tRNA 合成酶家族的成员,在真核生物中高度保守。TRMU 参与多种生理过程,包括线粒体蛋白质翻译、线粒体基因组转录和复制、氧化磷酸化以及细胞应激反应。TRMU 的突变与多种疾病有关,包括神经退行性疾病、代谢紊乱和癌症。TRMU 抑制剂已被开发用于治疗这些疾病。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b602/6800514/8ee5203e860a/1177f01.jpg

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