{"title":"Pooled Lentiviral-Delivery Genetic Screens","authors":"Federica Piccioni, Scott T. Younger, David E. Root","doi":"10.1002/cpmb.52","DOIUrl":null,"url":null,"abstract":"<p>Pooled cell-based screens of mammalian genetic perturbations enable systematic large-scale, even genome-scale, evaluation of gene function. Pooled screens introduce genetic perturbations into a cell population through viral transduction such that each cell integrates into its DNA a single or small number of library perturbations with barcodes identifying the perturbations. One then selects and physically isolates the subset of cells that exhibit the phenotype of interest. Sequencing the barcodes in the hit cells reveals which genes favored or inhibited the hit phenotype. Various genetic perturbations are possible, including CRISPR gene knockout, ectopic gene expression, and RNA interference. Regardless of the type of library being screened or the type of cell model being tested, such screens involve many common steps and procedures. This unit describes detailed experimental protocols for the key steps, and also highlights some of the key factors to achieving a well-powered, reproducible screen result. © 2018 by John Wiley & Sons, Inc.</p>","PeriodicalId":10734,"journal":{"name":"Current Protocols in Molecular Biology","volume":"121 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2018-01-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/cpmb.52","citationCount":"20","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current Protocols in Molecular Biology","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/cpmb.52","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"Biochemistry, Genetics and Molecular Biology","Score":null,"Total":0}
引用次数: 20
Abstract
Pooled cell-based screens of mammalian genetic perturbations enable systematic large-scale, even genome-scale, evaluation of gene function. Pooled screens introduce genetic perturbations into a cell population through viral transduction such that each cell integrates into its DNA a single or small number of library perturbations with barcodes identifying the perturbations. One then selects and physically isolates the subset of cells that exhibit the phenotype of interest. Sequencing the barcodes in the hit cells reveals which genes favored or inhibited the hit phenotype. Various genetic perturbations are possible, including CRISPR gene knockout, ectopic gene expression, and RNA interference. Regardless of the type of library being screened or the type of cell model being tested, such screens involve many common steps and procedures. This unit describes detailed experimental protocols for the key steps, and also highlights some of the key factors to achieving a well-powered, reproducible screen result. © 2018 by John Wiley & Sons, Inc.
慢病毒传递基因筛选
以细胞为基础的哺乳动物遗传干扰筛选使系统大规模,甚至基因组规模的基因功能评估成为可能。集合筛选通过病毒转导将遗传扰动引入细胞群体,使得每个细胞将单个或少量文库扰动整合到其DNA中,并用条形码识别这些扰动。然后选择并物理分离出表现出感兴趣表型的细胞子集。对被击中细胞中的条形码进行测序,可以揭示哪些基因有利于或抑制被击中的表型。各种遗传干扰是可能的,包括CRISPR基因敲除、异位基因表达和RNA干扰。无论正在筛选的库的类型或正在测试的细胞模型的类型如何,这种筛选都涉及许多常见的步骤和过程。本单元详细介绍了关键步骤的实验方案,并强调了一些关键因素,以实现良好的功率,可重复的筛选结果。©2018 by John Wiley &儿子,Inc。
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