Cargando…

RNA Pol II pausing facilitates phased pluripotency transitions by buffering transcription

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 un...

Descripción completa

Detalles Bibliográficos
Autores principales: Abuhashem, Abderhman, Chivu, Alexandra G., Zhao, Yixin, Rice, Edward J., Siepel, Adam, Danko, Charles G., Hadjantonakis, Anna-Katerina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9480856/
https://www.ncbi.nlm.nih.gov/pubmed/35981753
http://dx.doi.org/10.1101/gad.349565.122
_version_ 1784791135544147968
author Abuhashem, Abderhman
Chivu, Alexandra G.
Zhao, Yixin
Rice, Edward J.
Siepel, Adam
Danko, Charles G.
Hadjantonakis, Anna-Katerina
author_facet Abuhashem, Abderhman
Chivu, Alexandra G.
Zhao, Yixin
Rice, Edward J.
Siepel, Adam
Danko, Charles G.
Hadjantonakis, Anna-Katerina
author_sort Abuhashem, Abderhman
collection PubMed
description 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.
format Online
Article
Text
id pubmed-9480856
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Cold Spring Harbor Laboratory Press
record_format MEDLINE/PubMed
spelling pubmed-94808562023-01-01 RNA Pol II pausing facilitates phased pluripotency transitions by buffering transcription Abuhashem, Abderhman Chivu, Alexandra G. Zhao, Yixin Rice, Edward J. Siepel, Adam Danko, Charles G. Hadjantonakis, Anna-Katerina Genes Dev Research Paper 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. Cold Spring Harbor Laboratory Press 2022-07-01 /pmc/articles/PMC9480856/ /pubmed/35981753 http://dx.doi.org/10.1101/gad.349565.122 Text en © 2022 Abuhashem et al.; Published by Cold Spring Harbor Laboratory Press https://creativecommons.org/licenses/by-nc/4.0/This article is distributed exclusively by Cold Spring Harbor Laboratory Press for the first six months after the full-issue publication date (see http://genesdev.cshlp.org/site/misc/terms.xhtml). After six months, it is available under a Creative Commons License (Attribution-NonCommercial 4.0 International), as described at http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) .
spellingShingle Research Paper
Abuhashem, Abderhman
Chivu, Alexandra G.
Zhao, Yixin
Rice, Edward J.
Siepel, Adam
Danko, Charles G.
Hadjantonakis, Anna-Katerina
RNA Pol II pausing facilitates phased pluripotency transitions by buffering transcription
title RNA Pol II pausing facilitates phased pluripotency transitions by buffering transcription
title_full RNA Pol II pausing facilitates phased pluripotency transitions by buffering transcription
title_fullStr RNA Pol II pausing facilitates phased pluripotency transitions by buffering transcription
title_full_unstemmed RNA Pol II pausing facilitates phased pluripotency transitions by buffering transcription
title_short RNA Pol II pausing facilitates phased pluripotency transitions by buffering transcription
title_sort rna pol ii pausing facilitates phased pluripotency transitions by buffering transcription
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9480856/
https://www.ncbi.nlm.nih.gov/pubmed/35981753
http://dx.doi.org/10.1101/gad.349565.122
work_keys_str_mv AT abuhashemabderhman rnapoliipausingfacilitatesphasedpluripotencytransitionsbybufferingtranscription
AT chivualexandrag rnapoliipausingfacilitatesphasedpluripotencytransitionsbybufferingtranscription
AT zhaoyixin rnapoliipausingfacilitatesphasedpluripotencytransitionsbybufferingtranscription
AT riceedwardj rnapoliipausingfacilitatesphasedpluripotencytransitionsbybufferingtranscription
AT siepeladam rnapoliipausingfacilitatesphasedpluripotencytransitionsbybufferingtranscription
AT dankocharlesg rnapoliipausingfacilitatesphasedpluripotencytransitionsbybufferingtranscription
AT hadjantonakisannakaterina rnapoliipausingfacilitatesphasedpluripotencytransitionsbybufferingtranscription