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RNA polymerase II pausing can be retained or acquired during activation of genes involved in the epithelial to mesenchymal transition

Promoter-proximal RNA polymerase II (Pol II) pausing is implicated in the regulation of gene transcription. However, the mechanisms of pausing including its dynamics during transcriptional responses remain to be fully understood. We performed global analysis of short capped RNAs and Pol II Chromatin...

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Autores principales: Samarakkody, Ann, Abbas, Ata, Scheidegger, Adam, Warns, Jessica, Nnoli, Oscar, Jokinen, Bradley, Zarns, Kris, Kubat, Brooke, Dhasarathy, Archana, Nechaev, Sergei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4417172/
https://www.ncbi.nlm.nih.gov/pubmed/25820424
http://dx.doi.org/10.1093/nar/gkv263
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author Samarakkody, Ann
Abbas, Ata
Scheidegger, Adam
Warns, Jessica
Nnoli, Oscar
Jokinen, Bradley
Zarns, Kris
Kubat, Brooke
Dhasarathy, Archana
Nechaev, Sergei
author_facet Samarakkody, Ann
Abbas, Ata
Scheidegger, Adam
Warns, Jessica
Nnoli, Oscar
Jokinen, Bradley
Zarns, Kris
Kubat, Brooke
Dhasarathy, Archana
Nechaev, Sergei
author_sort Samarakkody, Ann
collection PubMed
description Promoter-proximal RNA polymerase II (Pol II) pausing is implicated in the regulation of gene transcription. However, the mechanisms of pausing including its dynamics during transcriptional responses remain to be fully understood. We performed global analysis of short capped RNAs and Pol II Chromatin Immunoprecipitation sequencing in MCF-7 breast cancer cells to map Pol II pausing across the genome, and used permanganate footprinting to specifically follow pausing during transcriptional activation of several genes involved in the epithelial to mesenchymal transition (EMT). We find that the gene for EMT master regulator Snail (SNAI1), but not Slug (SNAI2), shows evidence of Pol II pausing before activation. Transcriptional activation of the paused SNAI1 gene is accompanied by a further increase in Pol II pausing signal, whereas activation of non-paused SNAI2 gene results in the acquisition of a typical pausing signature. The increase in pausing signal reflects increased transcription initiation without changes in Pol II pausing. Activation of the heat shock HSP70 gene involves pausing release that speeds up Pol II turnover, but does not change pausing location. We suggest that Pol II pausing is retained during transcriptional activation and can further undergo regulated release in a signal-specific manner.
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spelling pubmed-44171722015-05-12 RNA polymerase II pausing can be retained or acquired during activation of genes involved in the epithelial to mesenchymal transition Samarakkody, Ann Abbas, Ata Scheidegger, Adam Warns, Jessica Nnoli, Oscar Jokinen, Bradley Zarns, Kris Kubat, Brooke Dhasarathy, Archana Nechaev, Sergei Nucleic Acids Res Gene regulation, Chromatin and Epigenetics Promoter-proximal RNA polymerase II (Pol II) pausing is implicated in the regulation of gene transcription. However, the mechanisms of pausing including its dynamics during transcriptional responses remain to be fully understood. We performed global analysis of short capped RNAs and Pol II Chromatin Immunoprecipitation sequencing in MCF-7 breast cancer cells to map Pol II pausing across the genome, and used permanganate footprinting to specifically follow pausing during transcriptional activation of several genes involved in the epithelial to mesenchymal transition (EMT). We find that the gene for EMT master regulator Snail (SNAI1), but not Slug (SNAI2), shows evidence of Pol II pausing before activation. Transcriptional activation of the paused SNAI1 gene is accompanied by a further increase in Pol II pausing signal, whereas activation of non-paused SNAI2 gene results in the acquisition of a typical pausing signature. The increase in pausing signal reflects increased transcription initiation without changes in Pol II pausing. Activation of the heat shock HSP70 gene involves pausing release that speeds up Pol II turnover, but does not change pausing location. We suggest that Pol II pausing is retained during transcriptional activation and can further undergo regulated release in a signal-specific manner. Oxford University Press 2015-04-30 2015-03-27 /pmc/articles/PMC4417172/ /pubmed/25820424 http://dx.doi.org/10.1093/nar/gkv263 Text en © The Author(s) 2015. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Gene regulation, Chromatin and Epigenetics
Samarakkody, Ann
Abbas, Ata
Scheidegger, Adam
Warns, Jessica
Nnoli, Oscar
Jokinen, Bradley
Zarns, Kris
Kubat, Brooke
Dhasarathy, Archana
Nechaev, Sergei
RNA polymerase II pausing can be retained or acquired during activation of genes involved in the epithelial to mesenchymal transition
title RNA polymerase II pausing can be retained or acquired during activation of genes involved in the epithelial to mesenchymal transition
title_full RNA polymerase II pausing can be retained or acquired during activation of genes involved in the epithelial to mesenchymal transition
title_fullStr RNA polymerase II pausing can be retained or acquired during activation of genes involved in the epithelial to mesenchymal transition
title_full_unstemmed RNA polymerase II pausing can be retained or acquired during activation of genes involved in the epithelial to mesenchymal transition
title_short RNA polymerase II pausing can be retained or acquired during activation of genes involved in the epithelial to mesenchymal transition
title_sort rna polymerase ii pausing can be retained or acquired during activation of genes involved in the epithelial to mesenchymal transition
topic Gene regulation, Chromatin and Epigenetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4417172/
https://www.ncbi.nlm.nih.gov/pubmed/25820424
http://dx.doi.org/10.1093/nar/gkv263
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