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利用遗传筛选发现抗病毒限制因子和途径。

Discovering antiviral restriction factors and pathways using genetic screens.

机构信息

Biomedical Sciences Research Complex, School of Biology, University of St Andrews, St Andrews, KY16 9ST, UK.

Division of Infection and Immunity, The Roslin Institute, University of Edinburgh, Edinburgh, EH25 9RG, UK.

出版信息

J Gen Virol. 2021 May;102(5). doi: 10.1099/jgv.0.001603.

Abstract

Viral infections activate the powerful interferon (IFN) response that induces the expression of several hundred IFN stimulated genes (ISGs). The principal role of this extensive response is to create an unfavourable environment for virus replication and to limit spread; however, untangling the biological consequences of this large response is complicated. In addition to a seemingly high degree of redundancy, several ISGs are usually required in combination to limit infection as individual ISGs often have low to moderate antiviral activity. Furthermore, what ISG or combination of ISGs are antiviral for a given virus is usually not known. For these reasons, and since the function(s) of many ISGs remains unexplored, genome-wide approaches are well placed to investigate what aspects of this response result in an appropriate, virus-specific phenotype. This review discusses the advances screening approaches have provided for the study of host defence mechanisms, including clustered regularly interspaced short palindromic repeats/CRISPR associated protein 9 (CRISPR/Cas9), ISG expression libraries and RNA interference (RNAi) technologies.

摘要

病毒感染会激活强大的干扰素 (IFN) 反应,诱导数百种干扰素刺激基因 (ISG) 的表达。这种广泛反应的主要作用是为病毒复制创造不利环境并限制其传播;然而,要理清这种大反应的生物学后果是很复杂的。除了看似高度冗余之外,通常需要几种 ISG 组合起来限制感染,因为单个 ISG 通常具有低到中等的抗病毒活性。此外,对于给定的病毒,哪些 ISG 或 ISG 组合具有抗病毒作用通常是未知的。由于这些原因,并且由于许多 ISG 的功能仍未得到探索,因此全基因组方法非常适合研究这种反应的哪些方面导致了适当的、特定于病毒的表型。本文综述了筛选方法在宿主防御机制研究方面的进展,包括成簇规律间隔短回文重复序列/CRISPR 相关蛋白 9 (CRISPR/Cas9)、ISG 表达文库和 RNA 干扰 (RNAi) 技术。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd7b/8295917/7c20110fc184/jgv-102-1603-g001.jpg

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