| Literature DB >> 29249356 |
Justin Brumbaugh1, Bruno Di Stefano1, Xiuye Wang2, Marti Borkent1, Elmira Forouzmand2, Katie J Clowers3, Fei Ji4, Benjamin A Schwarz1, Marian Kalocsay3, Stephen J Elledge5, Yue Chen6, Ruslan I Sadreyev7, Steven P Gygi3, Guang Hu8, Yongsheng Shi9, Konrad Hochedlinger10.
Abstract
Cell fate transitions involve rapid gene expression changes and global chromatin remodeling, yet the underlying regulatory pathways remain incompletely understood. Here, we identified the RNA-processing factor Nudt21 as a novel regulator of cell fate change using transcription-factor-induced reprogramming as a screening assay. Suppression of Nudt21 enhanced the generation of induced pluripotent stem cells, facilitated transdifferentiation into trophoblast stem cells, and impaired differentiation of myeloid precursors and embryonic stem cells, suggesting a broader role for Nudt21 in cell fate change. We show that Nudt21 directs differential polyadenylation of over 1,500 transcripts in cells acquiring pluripotency, although only a fraction changed protein levels. Remarkably, these proteins were strongly enriched for chromatin regulators, and their suppression neutralized the effect of Nudt21 during reprogramming. Collectively, our data uncover Nudt21 as a novel post-transcriptional regulator of cell fate and establish a direct, previously unappreciated link between alternative polyadenylation and chromatin signaling.Entities:
Keywords: Alternative polyadenylation; chromatin; embryonic stem cells; epigenetic regulation; induced pluripotent stem cells; induced trophoblast stem cells; microRNA; pluripotency; reprogramming; transdifferentiation
Mesh:
Substances:
Year: 2017 PMID: 29249356 PMCID: PMC5766360 DOI: 10.1016/j.cell.2017.11.023
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582