Large-scale image-based profiling of single-cell phenotypes in arrayed CRISPR-Cas9 gene perturbation screens

被引:42
|
作者
de Groot, Reinoud [1 ]
Luthi, Joel [1 ,2 ,3 ]
Lindsay, Helen [1 ]
Holtackers, Rene [1 ]
Pelkmans, Lucas [1 ]
机构
[1] Univ Zurich, Inst Mol Life Sci, Zurich, Switzerland
[2] ETH, Syst Biol PhD Program, Life Sci Zurich Grad Sch, Zurich, Switzerland
[3] Univ Zurich, Zurich, Switzerland
关键词
arrayed library; CRISPR-Cas9; functional genomics; nuclear pore complex; single-cell phenotypic profiling; HIGH-THROUGHPUT; CIRCUITS; PLATFORM; COMPLEX; DESIGN;
D O I
10.15252/msb.20178064
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
High-content imaging using automated microscopy and computer vision allows multivariate profiling of single-cell phenotypes. Here, we present methods for the application of the CISPR-Cas9 system in large-scale, image-based, gene perturbation experiments. We show that CRISPR-Cas9-mediated gene perturbation can be achieved in human tissue culture cells in a timeframe that is compatible with image-based phenotyping. We developed a pipeline to construct a large-scale arrayed library of 2,281 sequence-verified CRISPR-Cas9 targeting plasmids and profiled this library for genes affecting cellular morphology and the subcellular localization of components of the nuclear pore complex (NPC). We conceived a machine-learning method that harnesses genetic heterogeneity to score gene perturbations and identify phenotypically perturbed cells for in-depth characterization of gene perturbation effects. This approach enables genome-scale image-based multivariate gene perturbation profiling using CRISPR-Cas9.
引用
收藏
页数:10
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