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淋巴瘤细胞系中CRISPR-Cas9筛选方案

Protocols for CRISPR-Cas9 Screening in Lymphoma Cell Lines.

作者信息

Webster Daniel E, Roulland Sandrine, Phelan James D

机构信息

Lymphoid Malignancies Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.

CNRS, INSERM, Centre d'Immunologie de Marseille-Luminy, Aix-Marseille Universite, Marseille, France.

出版信息

Methods Mol Biol. 2019;1956:337-350. doi: 10.1007/978-1-4939-9151-8_16.

Abstract

Genome-wide screens are a powerful technique to dissect the complex network of genes regulating diverse cellular phenotypes. The recent adaptation of the CRISPR-Cas9 system for genome engineering has revolutionized functional genomic screening. Here, we present protocols used to introduce Cas9 into human lymphoma cell lines, produce high-titer lentivirus of a genome-wide sgRNA library, transduce and culture cells during the screen, isolate genomic DNA, and prepare a custom library for next-generation sequencing. These protocols were tailored for loss-of-function CRISPR screens in human lymphoma cell lines but are highly amenable for other experimental purposes.

摘要

全基因组筛选是剖析调控多种细胞表型的复杂基因网络的强大技术。CRISPR-Cas9系统最近在基因组工程中的应用彻底改变了功能基因组筛选。在这里,我们展示了将Cas9导入人淋巴瘤细胞系、生产全基因组sgRNA文库的高滴度慢病毒、在筛选过程中转导和培养细胞、分离基因组DNA以及制备用于下一代测序的定制文库所使用的方案。这些方案是针对人淋巴瘤细胞系中的功能丧失型CRISPR筛选量身定制的,但也非常适用于其他实验目的。

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