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一种优化的、无病毒的全基因组 CRISPR 筛选哺乳动物细胞的方法。

An optimized genome-wide, virus-free CRISPR screen for mammalian cells.

机构信息

The Novo Nordisk Foundation Center for Biosustainability, Technical University of Denmark, Lyngby, Denmark.

The Novo Nordisk Foundation Center for Biosustainability, University of California at San Diego, La Jolla, CA, USA.

出版信息

Cell Rep Methods. 2021 Aug 23;1(4). doi: 10.1016/j.crmeth.2021.100062. Epub 2021 Aug 4.

Abstract

Pooled CRISPR screens have been widely applied to mammalian and other organisms to elucidate the interplay between genes and phenotypes of interest. The most popular method for delivering the CRISPR components into mammalian cells is lentivirus based. However, because lentivirus is not always an option, virus-free protocols are starting to emerge. Here, we demonstrate an improved virus-free, genome-wide CRISPR screening platform for Chinese hamster ovary cells with 75,488 gRNAs targeting 15,028 genes. Each gRNA expression cassette in the library is precisely integrated into a genomic landing pad, resulting in a very high percentage of single gRNA insertions and minimal clonal variation. Using this platform, we perform a negative selection screen on cell proliferation that identifies 1,980 genes that affect proliferation and a positive selection screen on the toxic endoplasmic reticulum stress inducer, tunicamycin, that identifies 77 gene knockouts that improve survivability.

摘要

CRISPR 基因敲除文库筛选已广泛应用于哺乳动物和其他生物,以阐明感兴趣的基因和表型之间的相互作用。将 CRISPR 组件递送到哺乳动物细胞的最流行方法是基于慢病毒。然而,由于慢病毒并非总是一种选择,无病毒的方案开始出现。在这里,我们展示了一种改进的无病毒、全基因组 CRISPR 筛选平台,用于中国仓鼠卵巢细胞,该平台带有针对 15028 个基因的 75488 个 gRNA,文库中的每个 gRNA 表达盒都精确地整合到基因组着陆垫上,导致单 gRNA 插入的百分比非常高,克隆变异最小。使用该平台,我们对细胞增殖进行负选择筛选,鉴定出 1980 个影响增殖的基因,对毒性内质网应激诱导剂,衣霉素进行正选择筛选,鉴定出 77 个基因敲除,可提高存活率。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3445/9017179/f6bb24451bf9/fx1.jpg

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