The dynamic interactions between virus infections and nonsense-mediated decay.

IF 3.2 2区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Teun van der Klugt, Michiel van Gent
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引用次数: 0

Abstract

Humans are continuously exposed to a wide array of viruses that cause a significant amount of morbidity and mortality worldwide. Over recent years, the evolutionarily conserved host RNA degradation pathway nonsense-mediated decay (NMD) has emerged as a broad antiviral defense mechanism that controls infection of a variety of RNA and DNA viruses. Besides regulating the abundance of host transcripts, NMD directly destabilizes virus genomic RNA, replication intermediates, and viral transcripts to interfere with replication. In turn, viruses have evolved strategies to modulate cellular NMD activity or repurpose NMD factors to facilitate their replication. In this review, we describe our current understanding of the role of NMD in controlling virus infections as well as the strategies employed by viruses to interfere with NMD.

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病毒感染与无义介导的衰变之间的动态相互作用。
人类不断接触各种各样的病毒,这些病毒在世界范围内造成大量的发病率和死亡率。近年来,进化上保守的宿主RNA降解途径无义介导的衰变(NMD)已成为一种广泛的抗病毒防御机制,可控制多种RNA和DNA病毒的感染。除了调节宿主转录物的丰度外,NMD还直接破坏病毒基因组RNA、复制中间体和病毒转录物的稳定性,从而干扰复制。反过来,病毒已经进化出调节细胞NMD活性或重新利用NMD因子以促进其复制的策略。在这篇综述中,我们描述了我们目前对NMD在控制病毒感染中的作用的理解以及病毒干扰NMD的策略。
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来源期刊
Human molecular genetics
Human molecular genetics 生物-生化与分子生物学
CiteScore
6.90
自引率
2.90%
发文量
294
审稿时长
2-4 weeks
期刊介绍: Human Molecular Genetics concentrates on full-length research papers covering a wide range of topics in all aspects of human molecular genetics. These include: the molecular basis of human genetic disease developmental genetics cancer genetics neurogenetics chromosome and genome structure and function therapy of genetic disease stem cells in human genetic disease and therapy, including the application of iPS cells genome-wide association studies mouse and other models of human diseases functional genomics computational genomics In addition, the journal also publishes research on other model systems for the analysis of genes, especially when there is an obvious relevance to human genetics.
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