| Literature DB >> 34413171 |
Saba Parvez1, Chelsea Herdman2, Manu Beerens3, Korak Chakraborti1, Zachary P Harmer1, Jing-Ruey J Yeh4, Calum A MacRae3, H Joseph Yost2, Randall T Peterson1.
Abstract
CRISPR-Cas9 can be scaled up for large-scale screens in cultured cells, but CRISPR screens in animals have been challenging because generating, validating, and keeping track of large numbers of mutant animals is prohibitive. Here, we introduce Multiplexed Intermixed CRISPR Droplets (MIC-Drop), a platform combining droplet microfluidics, single-needle en masse CRISPR ribonucleoprotein injections, and DNA barcoding to enable large-scale functional genetic screens in zebrafish. The platform can efficiently identify genes responsible for morphological or behavioral phenotypes. In one application, we showed that MIC-Drop could identify small-molecule targets. Furthermore, in a MIC-Drop screen of 188 poorly characterized genes, we discovered several genes important for cardiac development and function. With the potential to scale to thousands of genes, MIC-Drop enables genome-scale reverse genetic screens in model organisms.Entities:
Mesh:
Year: 2021 PMID: 34413171 PMCID: PMC9083377 DOI: 10.1126/science.abi8870
Source DB: PubMed Journal: Science ISSN: 0036-8075 Impact factor: 63.714