剪接方面的所有差异:宿主选择性剪接改变了病毒-宿主冲突的格局

IF 6.2 2区 生物学 Q1 CELL BIOLOGY Seminars in cell & developmental biology Pub Date : 2023-09-15 DOI:10.1016/j.semcdb.2023.01.013
Joshua T. Mann , Brent A. Riley , Steven F. Baker
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引用次数: 1

摘要

选择性RNA剪接是一种共转录过程,它丰富地增加了蛋白质组的多样性,并根据细胞种类、谱系和激活状态进行动态调节。脊椎动物宿主中的病毒感染导致宿主转录组范围内的快速变化,而选择性剪接的调节可以对宿主转录组产生组合效应。最近,评估病毒感染期间宿主选择性剪接的全基因组研究有所增加,这与病毒与宿主剪接蛋白相互作用的先验知识很好地结合在一起。一个关键的挑战仍然是将这些个别事件如何指导全球变化,以及替代剪接是否是抵御或支持病毒感染的总体有利途径联系起来。在这里,我们介绍了选择性剪接的过程,讨论了如何分析剪接调控,并详细研究了病毒感染过程中全基因组和剪接因子的变化。我们试图强调该领域可以重点发展的领域,以及结合病毒-宿主共同进化的观点如何有利于这一新兴学科。
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All differential on the splicing front: Host alternative splicing alters the landscape of virus-host conflict

Alternative RNA splicing is a co-transcriptional process that richly increases proteome diversity, and is dynamically regulated based on cell species, lineage, and activation state. Virus infection in vertebrate hosts results in rapid host transcriptome-wide changes, and regulation of alternative splicing can direct a combinatorial effect on the host transcriptome. There has been a recent increase in genome-wide studies evaluating host alternative splicing during viral infection, which integrates well with prior knowledge on viral interactions with host splicing proteins. A critical challenge remains in linking how these individual events direct global changes, and whether alternative splicing is an overall favorable pathway for fending off or supporting viral infection. Here, we introduce the process of alternative splicing, discuss how to analyze splice regulation, and detail studies on genome-wide and splice factor changes during viral infection. We seek to highlight where the field can focus on moving forward, and how incorporation of a virus-host co-evolutionary perspective can benefit this burgeoning subject.

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来源期刊
CiteScore
15.10
自引率
1.40%
发文量
310
审稿时长
9.1 weeks
期刊介绍: Seminars in Cell and Developmental Biology is a review journal dedicated to keeping scientists informed of developments in the field of molecular cell and developmental biology, on a topic by topic basis. Each issue is thematic in approach, devoted to an important topic of interest to cell and developmental biologists, focusing on the latest advances and their specific implications. The aim of each issue is to provide a coordinated, readable, and lively review of a selected area, published rapidly to ensure currency.
期刊最新文献
Diverse genetic conflicts mediated by molecular mimicry and computational approaches to detect them Outside Front Cover Editorial Board/Publication Information From the cauldron of conflict: Endogenous gene regulation by piRNA and other modes of adaptation enabled by selfish transposable elements Outside Front Cover
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