| Literature DB >> 31005419 |
Davide Seruggia1, Martin Oti2, Pratibha Tripathi2, Matthew C Canver1, Lucy LeBlanc3, Dafne C Di Giammartino4, Michael J Bullen2, Christian M Nefzger5, Yu Bo Yang Sun5, Rick Farouni6, Jose M Polo5, Luca Pinello6, Effie Apostolou4, Jonghwan Kim3, Stuart H Orkin7, Partha Pratim Das8.
Abstract
Self-renewal and pluripotency of the embryonic stem cell (ESC) state are established and maintained by multiple regulatory networks that comprise transcription factors and epigenetic regulators. While much has been learned regarding transcription factors, the function of epigenetic regulators in these networks is less well defined. We conducted a CRISPR-Cas9-mediated loss-of-function genetic screen that identified two epigenetic regulators, TAF5L and TAF6L, components or co-activators of the GNAT-HAT complexes for the mouse ESC (mESC) state. Detailed molecular studies demonstrate that TAF5L/TAF6L transcriptionally activate c-Myc and Oct4 and their corresponding MYC and CORE regulatory networks. Besides, TAF5L/TAF6L predominantly regulate their target genes through H3K9ac deposition and c-MYC recruitment that eventually activate the MYC regulatory network for self-renewal of mESCs. Thus, our findings uncover a role of TAF5L/TAF6L in directing the MYC regulatory network that orchestrates gene expression programs to control self-renewal for the maintenance of mESC state.Entities:
Keywords: CRISPR; ESC; MYC; OCT4; TAF5L; TAF6L
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Year: 2019 PMID: 31005419 PMCID: PMC6671628 DOI: 10.1016/j.molcel.2019.03.025
Source DB: PubMed Journal: Mol Cell ISSN: 1097-2765 Impact factor: 17.970