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通过全基因组 CRISPR 筛选可视化黄病毒-宿主相互作用全景图。

Flavivirus-Host Interaction Landscape Visualized through Genome-Wide CRISPR Screens.

机构信息

Centre for Infectious Disease Research, Indian Institute of Science, Bengaluru 560012, India.

Microbiology & Cell Biology, Indian Institute of Science, Bengaluru 560012, India.

出版信息

Viruses. 2022 Sep 30;14(10):2164. doi: 10.3390/v14102164.

Abstract

Flaviviruses comprise several important human pathogens which cause significant morbidity and mortality worldwide. Like any other virus, they are obligate intracellular parasites. Therefore, studying the host cellular factors that promote or restrict their replication and pathogenesis becomes vital. Since inhibiting the host dependency factors or activating the host restriction factors can suppress the viral replication and propagation in the cell, identifying them reveals potential targets for antiviral therapeutics. Clustered regularly interspaced short palindromic repeats (CRISPR) technology has provided an effective means of producing customizable genetic modifications and performing forward genetic screens in a broad spectrum of cell types and organisms. The ease, rapidity, and high reproducibility of CRISPR technology have made it an excellent tool for carrying out genome-wide screens to identify and characterize viral host dependency factors systematically. Here, we review the insights from various Genome-wide CRISPR screens that have advanced our understanding of Flavivirus-Host interactions.

摘要

黄病毒属包括几种重要的人类病原体,在全球范围内造成了重大的发病率和死亡率。与其他任何病毒一样,它们是专性细胞内寄生虫。因此,研究促进或限制其复制和发病机制的宿主细胞因子变得至关重要。由于抑制宿主依赖性因子或激活宿主限制因子可以抑制病毒在细胞中的复制和传播,因此识别它们可以揭示抗病毒治疗的潜在靶点。成簇规律间隔短回文重复序列 (CRISPR) 技术为在广泛的细胞类型和生物体中进行定制基因修饰和进行正向遗传筛选提供了有效手段。CRISPR 技术的简便性、快速性和高重复性使其成为进行全基因组筛选的绝佳工具,可系统地识别和表征病毒宿主依赖性因子。在这里,我们回顾了来自各种全基因组 CRISPR 筛选的见解,这些见解加深了我们对黄病毒-宿主相互作用的理解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/869a/9609550/7cac1bf9b587/viruses-14-02164-g001.jpg

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