Division of Hematology/Oncology, Boston Children's Hospital and Department of Pediatric Oncology, Dana-Farber Cancer Institute (DFCI), Harvard Stem Cell Institute, Harvard Medical School, Boston, MA 02115, USA.
Department of Anatomy and Developmental Biology, Monash University, Wellington Road, Clayton, VIC 3800, Australia; Development and Stem Cells Program, Monash Biomedicine Discovery Institute, Wellington Road, Clayton, VIC 3800, Australia.
Mol Cell. 2019 Jun 20;74(6):1148-1163.e7. doi: 10.1016/j.molcel.2019.03.025. Epub 2019 Apr 17.
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.
胚胎干细胞 (ESC) 状态的自我更新和多能性是由多个调节网络建立和维持的,这些调节网络包括转录因子和表观遗传调节剂。虽然已经了解了很多关于转录因子的知识,但这些网络中表观遗传调节剂的功能还不太明确。我们进行了 CRISPR-Cas9 介导的功能丧失遗传筛选,鉴定出两个表观遗传调节剂,TAF5L 和 TAF6L,它们是用于小鼠 ESC(mESC)状态的 GNAT-HAT 复合物的组成部分或共激活因子。详细的分子研究表明,TAF5L/TAF6L 转录激活 c-Myc 和 Oct4 及其相应的 MYC 和 CORE 调节网络。此外,TAF5L/TAF6L 主要通过 H3K9ac 沉积和 c-MYC 募集来调节其靶基因,最终激活 MYC 调节网络,以维持 mESC 的自我更新。因此,我们的发现揭示了 TAF5L/TAF6L 在指导 MYC 调节网络中的作用,该网络协调基因表达程序,以控制自我更新,维持 mESC 状态。