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控制病毒基因表达的RNA杠杆和开关。

RNA levers and switches controlling viral gene expression.

作者信息

Allan Matthew F, Brivanlou Amir, Rouskin Silvi

机构信息

Department of Microbiology, Harvard Medical School, Boston, MA 02115, USA; Department of Biological Engineering, Massachusetts Institute of Technology, Cambridge, MA 02139, USA; Computational and Systems Biology, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.

Department of Microbiology, Harvard Medical School, Boston, MA 02115, USA.

出版信息

Trends Biochem Sci. 2023 Apr;48(4):391-406. doi: 10.1016/j.tibs.2022.12.002. Epub 2023 Jan 27.

Abstract

RNA viruses are diverse and abundant pathogens that are responsible for numerous human diseases. RNA viruses possess relatively compact genomes and have therefore evolved multiple mechanisms to maximize their coding capacities, often by encoding overlapping reading frames. These reading frames are then decoded by mechanisms such as alternative splicing and ribosomal frameshifting to produce multiple distinct proteins. These solutions are enabled by the ability of the RNA genome to fold into 3D structures that can mimic cellular RNAs, hijack host proteins, and expose or occlude regulatory protein-binding motifs to ultimately control key process in the viral life cycle. We highlight recent findings focusing on less conventional mechanisms of gene expression and new discoveries on the role of RNA structures.

摘要

RNA病毒是多样且丰富的病原体,可引发多种人类疾病。RNA病毒拥有相对紧凑的基因组,因此进化出了多种机制来最大化其编码能力,通常是通过编码重叠阅读框来实现。然后,这些阅读框通过选择性剪接和核糖体移码等机制进行解码,以产生多种不同的蛋白质。RNA基因组能够折叠成可模拟细胞RNA、劫持宿主蛋白并暴露或封闭调节性蛋白结合基序的三维结构,从而实现这些机制,最终控制病毒生命周期中的关键过程。我们重点介绍了近期关于不太常规的基因表达机制的研究发现以及RNA结构作用的新发现。

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