arrow
返回

High-content CRISPR screening

delete2022-02-10
delete0
PRE
AI
C
Christoph Bock *
P
Paul Datlinger
F
Florence Chardon
M
Matthew A. Coelho
M
Matthew B. Dong
K
Keith A. Lawson
T
Tian Lu
L
Laetitia Maroc
T
Thomas M. Norman
B
Bicna Song
G
Geoff Stanley
S
Sidi Chen
M
Mathew Garnett
李薇 封面图
李薇 (Wei Li)
J
Jason Moffat
L
Lei S. Qi
R
Rebecca S. Shapiro
J
Jay Shendure
J
Jonathan S. Weissman
X
Xiaowei Zhuang
DOI:10.1038/s43586-021-00093-4delete
delete原文链接
delete分享
delete收藏
摘要

摘要

En 中文
CRISPR screens are a powerful source of biological discovery, enabling the unbiased interrogation of gene function in a wide range of applications and species. In pooled CRISPR screens, various genetically encoded perturbations are introduced into pools of cells. The targeted cells proliferate under a biological challenge such as cell competition, drug treatment or viral infection. Subsequently, the perturbation-induced effects are evaluated by sequencing-based counting of the guide RNAs that specify each perturbation. The typical results of such screens are ranked lists of genes that confer sensitivity or resistance to the biological challenge of interest. Contributing to the broad utility of CRISPR screens, adaptations of the core CRISPR technology make it possible to activate, silence or otherwise manipulate the target genes. Moreover, high-content read-outs such as single-cell RNA sequencing and spatial imaging help characterize screened cells with unprecedented detail. Dedicated software tools facilitate bioinformatic analysis and enhance reproducibility. CRISPR screening has unravelled various molecular mechanisms in basic biology, medical genetics, cancer research, immunology, infectious diseases, microbiology and other fields. This Primer describes the basic and advanced concepts of CRISPR screening and its application as a flexible and reliable method for biological discovery, biomedical research and drug development — with a special emphasis on high-content methods that make it possible to obtain detailed biological insights directly as part of the screen. CRISPR screening is a high-throughput approach for identifying genes, pathways and mechanisms involved in a given phenotype or biological process. High-content read-outs of these screens, such as imaging and single-cell sequencing techniques, have further broadened its applicability. This Primer by Bock et al. describes the main concepts of CRISPR screening and gives examples of its application as a method for biological discovery, with a focus on the use of high-content read-outs.

期刊

Nature Reviews Methods Primers 封面图
Nature Reviews Methods Primers
IF:
56
论文数:
235
被引数:
9.7K

机构

S
Stanford University
学者数:
5.8K
论文数: 1.9K
被引数: 1.4W
U
University of Toronto
学者数:
4.7K
论文数: 1.6K
被引数: 1.3W
C
children's national hospital
学者数:
122
论文数: 47
被引数: 0
U
University of Guelph
学者数:
617
论文数: 279
被引数: 1.3K
W
Wellcome Sanger Institute
学者数:
1.1K
论文数: 170
被引数: 1
Y
Yale University School of Medicine
学者数:
990
论文数: 271
被引数: 2
U
university of washington
学者数:
4.5K
论文数: 1.5K
被引数: 9.7K
H
Harvard University
学者数:
5.7K
论文数: 2.0K
被引数: 3.2W
U
university of california
学者数:
1.2W
论文数: 3.9K
被引数: 31
学者 查看更多机构
引用论文

引用论文

CRISPR-Cas9 Knockin Mice for Genome Editing and Cancer Modeling用于基因组编辑和癌症建模的CRISPR-Cas9敲入小鼠
errCell
IF0
err2014-10-01
err0
errOAAI
errRandall J. Platt; Sidi Chen; Yang Zhou; Michael J. Yim; Lukasz Swiech; Hannah R. Kempton; James E. Dahlman; Oren Parnas; Thomas M. Eisenhaure; Marko Jovanovic; Daniel B. Graham; Siddharth Jhunjhunwala; Matthias Heidenreich; Ramnik J. Xavier; Robert Langer; Daniel G. Anderson; Nir Hacohen; Aviv Regev; Guoping Feng; Phillip A. Sharp; Feng Zhang
err分享
err收藏
Discovery and functional interrogation of SARS-CoV-2 RNA-host protein interactions
errCell
IF0
err2021-04-01
err0
errOAAI
errRyan A. Flynn; Julia A. Belk; Yanyan Qi; Yuki Yasumoto; Jin Wei; Mia Madel Alfajaro; Quanming Shi; Maxwell R. Mumbach; Aditi Limaye; Peter C. DeWeirdt; Cameron O. Schmitz; Kevin R. Parker; Elizabeth Woo; Howard Y. Chang; Tamas L. Horvath; Jan E. Carette; Carolyn R. Bertozzi; Craig B. Wilen; Ansuman T. Satpathy
err分享
err收藏
err分享
err收藏
Genome-wide CRISPR screen identifies TMEM41B as a gene required for autophagosome formation
err2018-08-09
err156
errOAAI
errMorita, Keigo; Hama, Yutaro; Izume, Tamaki; Tamura, Norito; Ueno, Toshihide; Yamashita, Yoshihiro; Sakamaki, Yuriko; Mimura, Kaito; Morishita, Hideaki; Shihoya, Wataru; Nureki, Osamu; Mano, Hiroyuki; Mizushima, Noboru
err分享
err收藏
err分享
err收藏
CRISPR/Cas9 screening using unique molecular identifiers使用独特的分子标识符进行CRISPR/Cas9筛选
err2017-10-09
err49
errOAAI
errSchmierer, Bernhard; Botla, Sandeep K.; Zhang, Jilin; Turunen, Mikko; Kivioja, Teemu; Taipale, Jussi
err分享
err收藏
A CRISPR Dropout Screen Identifies Genetic Vulnerabilities and Therapeutic Targets in Acute Myeloid LeukemiaCRISPR Dropout筛选确定了急性髓系白血病的遗传脆弱性和治疗靶点
err2016-10-01
err501
errOAAI
errTzelepis, Konstantinos; Koike-Yusa, Hiroko; De Braekeleer, Etienne; Li, Yilong; Metzakopian, Emmanouil; Dovey, Oliver M.; Mupo, Annalisa; Grinkevich, Vera; Li, Meng; Mazan, Milena; Gozdecka, Malgorzata; Ohnishi, Shuhei; Cooper, Jonathan; Patel, Miten; McKerrell, Thomas; Chen, Bin; Domingues, Ana Filipa; Gallipoli, Paolo; Teichmann, Sarah; Ponstingl, Hannes; McDermott, Ultan; Saez-Rodriguez, Julio; Huntly, Brian J. P.; Iorio, Francesco; Pina, Cristina; Vassiliou, George S.; Yusa, Kosuke
err分享
err收藏
Engineered anti-CRISPR proteins for optogenetic control of CRISPR-Cas9
err2018-10-30
err163
PREAI
errBubeck, Felix; Hoffmann, Mareike D.; Harteveld, Zander; Aschenbrenner, Sabine; Bietz, Andreas; Waldhauer, Max C.; Boerner, Kathleen; Fakhiri, Julia; Schmelas, Carolin; Dietz, Laura; Grimm, Dirk; Correia, Bruno E.; Eils, Roland; Niopek, Dominik
err分享
err收藏
学者 查看更多内容