RNA Pol II pausing facilitates phased pluripotency transitions by buffering transcription Journal Article


Authors: Abuhashem, A.; Chivu, A. G.; Zhao, Y.; Rice, E. J.; Siepel, A.; Danko, C. G.; Hadjantonakis, A. K.
Article Title: RNA Pol II pausing facilitates phased pluripotency transitions by buffering transcription
Abstract: Promoter-proximal RNA Pol II pausing is a critical step in transcriptional control. Pol II pausing has been predominantly studied in tissue culture systems. While Pol II pausing has been shown to be required for mammalian development, the phenotypic and mechanistic details of this requirement are unknown. Here, we found that loss of Pol II pausing stalls pluripotent state transitions within the epiblast of the early mouse embryo. Using Nelfb−/− mice and a NELFB degron mouse pluripotent stem cell model, we show that embryonic stem cells (ESCs) representing the naïve state of pluripotency successfully initiate a transition program but fail to balance levels of induced and repressed genes and enhancers in the absence of NELF. We found an increase in chromatin-associated NELF during transition from the naïve to later pluripotent states. Overall, our work defines the acute and long-term molecular consequences of NELF loss and reveals a role for Pol II pausing in the pluripotency continuum as a modulator of cell state transitions. © 2022 Abuhashem et al.
Keywords: controlled study; promoter region; nonhuman; animal cell; mouse; embryonic stem cell; animal experiment; transcription factor; transcription regulation; chromatin; transcription; embryonic stem cells; gene regulatory network; pluripotent stem cell; rna polymerase ii; mouse embryo; epiblast; ectoderm; pluripotency; male; female; article; pausing; nelf; degron; dtag
Journal Title: Genes and Development
Volume: 36
Issue: 13-14
ISSN: 0890-9369
Publisher: Cold Spring Harbor Laboratory Press  
Date Published: 2022-07-01
Start Page: 770
End Page: 789
Language: English
DOI: 10.1101/gad.349565.122
PUBMED: 35981753
PROVIDER: scopus
PMCID: PMC9480856
DOI/URL:
Notes: Article -- Export Date: 1 November 2022 -- Source: Scopus
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