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CRISPR 筛选猪 sgRNA 文库鉴定与日本脑炎病毒复制相关的宿主因子。

CRISPR screening of porcine sgRNA library identifies host factors associated with Japanese encephalitis virus replication.

机构信息

Key Laboratory of Agricultural Animal Genetics, Breeding and Reproduction of Ministry of Education & Key Lab of Swine Genetics and Breeding of Ministry of Agriculture and Rural Affairs, Huazhong Agricultural University, 430070, Wuhan, P. R. China.

The Cooperative Innovation Center for Sustainable Pig Production, Huazhong Agricultural University, 430070, Wuhan, P. R. China.

出版信息

Nat Commun. 2020 Oct 14;11(1):5178. doi: 10.1038/s41467-020-18936-1.

Abstract

Japanese encephalitis virus (JEV) is a mosquito-borne zoonotic flavivirus that causes encephalitis and reproductive disorders in mammalian species. However, the host factors critical for its entry, replication, and assembly are poorly understood. Here, we design a porcine genome-scale CRISPR/Cas9 knockout (PigGeCKO) library containing 85,674 single guide RNAs targeting 17,743 protein-coding genes, 11,053 long ncRNAs, and 551 microRNAs. Subsequently, we use the PigGeCKO library to identify key host factors facilitating JEV infection in porcine cells. Several previously unreported genes required for JEV infection are highly enriched post-JEV selection. We conduct follow-up studies to verify the dependency of JEV on these genes, and identify functional contributions for six of the many candidate JEV-related host genes, including EMC3 and CALR. Additionally, we identify that four genes associated with heparan sulfate proteoglycans (HSPGs) metabolism, specifically those responsible for HSPGs sulfurylation, facilitate JEV entry into porcine cells. Thus, beyond our development of the largest CRISPR-based functional genomic screening platform for pig research to date, this study identifies multiple potentially vulnerable targets for the development of medical and breeding technologies to treat and prevent diseases caused by JEV.

摘要

日本脑炎病毒(JEV)是一种经蚊子传播的动物源性黄病毒,可引起哺乳动物脑炎和生殖障碍。然而,其进入、复制和组装所必需的宿主因素仍知之甚少。在这里,我们设计了一个包含 85674 个靶向 17743 个蛋白编码基因、11053 个长非编码 RNA 和 551 个 microRNA 的猪基因组规模的 CRISPR/Cas9 敲除(PigGeCKO)文库。随后,我们使用 PigGeCKO 文库来鉴定有助于猪细胞中 JEV 感染的关键宿主因素。在 JEV 选择后,几个以前未报道的与 JEV 感染相关的基因被高度富集。我们进行了后续研究来验证 JEV 对这些基因的依赖性,并鉴定了六个候选 JEV 相关宿主基因中的功能贡献,包括 EMC3 和 CALR。此外,我们还发现与硫酸乙酰肝素蛋白聚糖(HSPGs)代谢相关的四个基因,特别是负责 HSPGs 硫酯化的基因,促进了 JEV 进入猪细胞。因此,除了开发迄今为止最大的基于 CRISPR 的猪研究功能基因组筛选平台外,本研究还确定了多个潜在的脆弱靶点,可用于开发医学和繁殖技术来治疗和预防 JEV 引起的疾病。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d7e/7560704/29ec97093a85/41467_2020_18936_Fig1_HTML.jpg

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