Huang Shiying, Baskin Jeremy M
Department of Chemistry and Chemical Biology, Cornell University, Ithaca, NY 14853 USA.
Weill Institute for Cell and Molecular Biology, Cornell University, Ithaca, NY 14853 USA.
Isr J Chem. 2023 Feb;63(1-2). doi: 10.1002/ijch.202200056. Epub 2022 Oct 18.
In less than a decade, CRISPR screening has revolutionized forward genetics and cell and molecular biology. Advances in screening technologies, including sgRNA libraries, Cas9-expressing cell lines, and streamlined sequencing pipelines, have democratized pooled CRISPR screens at genome-wide scale. Initially, many such screens were survival-based, identifying essential genes in physiological or perturbed processes. With the application of new chemical biology tools to CRISPR screening, the phenotypic space is no longer limited to live/dead selection or screening for levels of conventional fluorescent protein reporters. Further, the resolution has been increased from cell populations to single cells or even the subcellular level. We highlight advances in pooled CRISPR screening, powered by chemical biology, that have expanded phenotypic space, resolution, scope, and scalability as well as strengthened the CRISPR/Cas enzyme toolkit to enable biological hypothesis generation and discovery.
在不到十年的时间里,CRISPR筛选彻底改变了正向遗传学以及细胞与分子生物学。筛选技术的进步,包括sgRNA文库、表达Cas9的细胞系以及简化的测序流程,使得全基因组规模的CRISPR混合筛选变得更加普及。最初,许多此类筛选都是基于生存的,旨在识别生理过程或受干扰过程中的必需基因。随着新的化学生物学工具应用于CRISPR筛选,表型空间不再局限于活/死选择或对传统荧光蛋白报告基因水平的筛选。此外,分辨率已从细胞群体提高到单细胞甚至亚细胞水平。我们重点介绍了由化学生物学推动的CRISPR混合筛选的进展,这些进展扩大了表型空间、分辨率、范围和可扩展性,同时强化了CRISPR/Cas酶工具包,以促进生物学假设的提出和发现。