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宿主热休克蛋白MRJ/DNAJB6调节病毒感染。

The Host Heat Shock Protein MRJ/DNAJB6 Modulates Virus Infection.

作者信息

Ko Shih-Han, Huang Li-Min, Tarn Woan-Yuh

机构信息

Institute of Clinical Medicine, National Taiwan University College of Medicine, Taipei, Taiwan.

Department of Pediatrics, National Taiwan University Children's Hospital, National Taiwan University College of Medicine, Taipei, Taiwan.

出版信息

Front Microbiol. 2019 Dec 11;10:2885. doi: 10.3389/fmicb.2019.02885. eCollection 2019.

Abstract

A variety of pathogens take advantage of cellular heat shock proteins (HSPs) to complete their life cycle and exert pathogenic effects. MRJ (DNAJB6), a member of the heat shock protein 40 family, acts as a molecular chaperone for a wide range of cellular processes. MRJ mutations are linked to human diseases, such as muscular dystrophy and neurodegenerative diseases. There are two MRJ isoforms generated by alternative use of terminal exons, which differ in their C-terminus. This mini-review summarizes how these two MRJ isoforms participate differentially in viral production and virulence, and the possibility for MRJ as a therapeutic target.

摘要

多种病原体利用细胞热休克蛋白(HSPs)来完成其生命周期并发挥致病作用。热休克蛋白40家族成员MRJ(DNAJB6)在广泛的细胞过程中充当分子伴侣。MRJ突变与人类疾病相关,如肌肉萎缩症和神经退行性疾病。通过末端外显子的选择性使用产生了两种MRJ异构体,它们的C末端不同。这篇小型综述总结了这两种MRJ异构体如何不同地参与病毒产生和毒力,以及MRJ作为治疗靶点的可能性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5218/6917656/4825b95d10b7/fmicb-10-02885-g001.jpg

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