| Literature DB >> 30970261 |
Barbara Mair1, Jelena Tomic1, Sanna N Masud2, Peter Tonge3, Alexander Weiss1, Matej Usaj1, Amy Hin Yan Tong1, Jamie J Kwan4, Kevin R Brown1, Emily Titus3, Michael Atkins5, Katherine S K Chan1, Lise Munsie3, Andrea Habsid1, Hong Han1, Marion Kennedy4, Brenda Cohen4, Gordon Keller5, Jason Moffat6.
Abstract
Human pluripotent stem cells (hPSCs) provide an invaluable tool for modeling diseases and hold promise for regenerative medicine. For understanding pluripotency and lineage differentiation mechanisms, a critical first step involves systematically cataloging essential genes (EGs) that are indispensable for hPSC fitness, defined as cell reproduction in this study. To map essential genetic determinants of hPSC fitness, we performed genome-scale loss-of-function screens in an inducible Cas9 H1 hPSC line cultured on feeder cells and laminin to identify EGs. Among these, we found FOXH1 and VENTX, genes that encode transcription factors previously implicated in stem cell biology, as well as an uncharacterized gene, C22orf43/DRICH1. hPSC EGs are substantially different from other human model cell lines, and EGs in hPSCs are highly context dependent with respect to different growth substrates. Our CRISPR screens establish parameters for genome-wide screens in hPSCs, which will facilitate the characterization of unappreciated genetic regulators of hPSC biology.Entities:
Keywords: DRICH1; essential genes; functional genomics; genome-wide CRISPR screen; human pluripotent stem cells
Mesh:
Year: 2019 PMID: 30970261 DOI: 10.1016/j.celrep.2019.02.041
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423