| First Author | Hackett JA | Year | 2018 |
| Journal | Nat Commun | Volume | 9 |
| Issue | 1 | Pages | 4292 |
| PubMed ID | 30327475 | Mgi Jnum | J:267754 |
| Mgi Id | MGI:6267860 | Doi | 10.1038/s41467-018-06230-0 |
| Citation | Hackett JA, et al. (2018) Tracing the transitions from pluripotency to germ cell fate with CRISPR screening. Nat Commun 9(1):4292 |
| abstractText | Early mammalian development entails transit through naive pluripotency towards post-implantation epiblast, which subsequently gives rise to primordial germ cells (PGC), the founding germline population. To investigate these cell fate transitions, we developed a compound-reporter to track cellular identity in a model of PGC specification (PGC-like cells; PGCLC), and coupled it with genome-wide CRISPR screening. We identify key genes both for exit from pluripotency and for acquisition of PGC fate, and characterise a central role for the transcription regulators Nr5a2 and Zfp296 in germline ontogeny. Abrogation of these genes results in widespread activation (Nr5a2(-/-)) or inhibition (Zfp296(-/-)) of WNT pathway factors in PGCLC. This leads to aberrant upregulation of the somatic programme or failure to activate germline genes, respectively, and consequently loss of germ cell identity. Our study places Zfp296 and Nr5a2 as key components of an expanded PGC gene regulatory network, and outlines a transferable strategy for identifying critical regulators of complex cell fate decisions. |
