Genome-Scale CRISPR Screening for Regulators of Cell Fate Transitions

Methods Mol Biol. 2021:2214:91-108. doi: 10.1007/978-1-0716-0958-3_7.

Abstract

Knockout CRISPR screening enables the unbiased discovery of genes with a functional role in almost any cellular or molecular process of interest. The approach couples a genome-scale library of guide RNA (gRNA), the Cas9 endonuclease, and a faithful phenotypic read-out to systematically identify candidate genes via their loss-of-function effect. Here we provide a detailed description of the CRISPR screen protocol and outline how to apply it to decipher the gene networks that underlie developmental cell fate decisions. As a paradigm we use the in vitro model of cell state transition(s) from naive pluripotency to primordial germ cell (PGC) fate, exploiting the Stella-GFP:Esg1-tdTomato (SGET) mouse ESC line. The principles in this protocol can be readily adapted to characterize lineage regulators for other cell fate models and/or for other species.

Keywords: CRISPR; Germ cell; Lentivirus; Lineage regulator; PGC; Pluripotency; Protocol; Stem cell.

MeSH terms

  • Animals
  • CRISPR-Cas Systems*
  • Cell Differentiation
  • Cell Line
  • Embryonic Germ Cells / cytology*
  • Embryonic Germ Cells / metabolism
  • Gene Regulatory Networks
  • HEK293 Cells
  • Humans
  • Mice
  • Mouse Embryonic Stem Cells / cytology*
  • Mouse Embryonic Stem Cells / metabolism
  • RNA, Guide, CRISPR-Cas Systems / genetics
  • Transduction, Genetic

Substances

  • RNA, Guide, CRISPR-Cas Systems