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Elongin A regulates transcription in vivo through enhanced RNA polymerase processivity
Elongin is an RNA polymerase II (RNAPII)-associated factor that has been shown to stimulate transcriptional elongation in vitro. The Elongin complex is thought to be required for transcriptional induction in response to cellular stimuli and to ubiquitinate RNAPII in response to DNA damage. Yet, the...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Biochemistry and Molecular Biology
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7948402/ https://www.ncbi.nlm.nih.gov/pubmed/33298525 http://dx.doi.org/10.1074/jbc.RA120.015876 |
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author | Wang, Yating Hou, Liming Ardehali, M. Behfar Kingston, Robert E. Dynlacht, Brian D. |
author_facet | Wang, Yating Hou, Liming Ardehali, M. Behfar Kingston, Robert E. Dynlacht, Brian D. |
author_sort | Wang, Yating |
collection | PubMed |
description | Elongin is an RNA polymerase II (RNAPII)-associated factor that has been shown to stimulate transcriptional elongation in vitro. The Elongin complex is thought to be required for transcriptional induction in response to cellular stimuli and to ubiquitinate RNAPII in response to DNA damage. Yet, the impact of the Elongin complex on transcription in vivo has not been well studied. Here, we performed comprehensive studies of the role of Elongin A, the largest subunit of the Elongin complex, on RNAPII transcription genome-wide. Our results suggest that Elongin A localizes to actively transcribed regions and potential enhancers, and the level of recruitment correlated with transcription levels. We also identified a large group of factors involved in transcription as Elongin A–associated factors. In addition, we found that loss of Elongin A leads to dramatically reduced levels of serine2-phosphorylated, but not total, RNAPII, and cells depleted of Elongin A show stronger promoter RNAPII pausing, suggesting that Elongin A may be involved in the release of paused RNAPII. Our RNA-seq studies suggest that loss of Elongin A did not alter global transcription, and unlike prior in vitro studies, we did not observe a dramatic impact on RNAPII elongation rates in our cell-based nascent RNA-seq experiments upon Elongin A depletion. Taken together, our studies provide the first comprehensive analysis of the role of Elongin A in regulating transcription in vivo. Our studies also revealed that unlike prior in vitro findings, depletion of Elongin A has little impact on global transcription profiles and transcription elongation in vivo. |
format | Online Article Text |
id | pubmed-7948402 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Society for Biochemistry and Molecular Biology |
record_format | MEDLINE/PubMed |
spelling | pubmed-79484022021-03-19 Elongin A regulates transcription in vivo through enhanced RNA polymerase processivity Wang, Yating Hou, Liming Ardehali, M. Behfar Kingston, Robert E. Dynlacht, Brian D. J Biol Chem Research Article Elongin is an RNA polymerase II (RNAPII)-associated factor that has been shown to stimulate transcriptional elongation in vitro. The Elongin complex is thought to be required for transcriptional induction in response to cellular stimuli and to ubiquitinate RNAPII in response to DNA damage. Yet, the impact of the Elongin complex on transcription in vivo has not been well studied. Here, we performed comprehensive studies of the role of Elongin A, the largest subunit of the Elongin complex, on RNAPII transcription genome-wide. Our results suggest that Elongin A localizes to actively transcribed regions and potential enhancers, and the level of recruitment correlated with transcription levels. We also identified a large group of factors involved in transcription as Elongin A–associated factors. In addition, we found that loss of Elongin A leads to dramatically reduced levels of serine2-phosphorylated, but not total, RNAPII, and cells depleted of Elongin A show stronger promoter RNAPII pausing, suggesting that Elongin A may be involved in the release of paused RNAPII. Our RNA-seq studies suggest that loss of Elongin A did not alter global transcription, and unlike prior in vitro studies, we did not observe a dramatic impact on RNAPII elongation rates in our cell-based nascent RNA-seq experiments upon Elongin A depletion. Taken together, our studies provide the first comprehensive analysis of the role of Elongin A in regulating transcription in vivo. Our studies also revealed that unlike prior in vitro findings, depletion of Elongin A has little impact on global transcription profiles and transcription elongation in vivo. American Society for Biochemistry and Molecular Biology 2020-12-13 /pmc/articles/PMC7948402/ /pubmed/33298525 http://dx.doi.org/10.1074/jbc.RA120.015876 Text en © 2020 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Research Article Wang, Yating Hou, Liming Ardehali, M. Behfar Kingston, Robert E. Dynlacht, Brian D. Elongin A regulates transcription in vivo through enhanced RNA polymerase processivity |
title | Elongin A regulates transcription in vivo through enhanced RNA polymerase processivity |
title_full | Elongin A regulates transcription in vivo through enhanced RNA polymerase processivity |
title_fullStr | Elongin A regulates transcription in vivo through enhanced RNA polymerase processivity |
title_full_unstemmed | Elongin A regulates transcription in vivo through enhanced RNA polymerase processivity |
title_short | Elongin A regulates transcription in vivo through enhanced RNA polymerase processivity |
title_sort | elongin a regulates transcription in vivo through enhanced rna polymerase processivity |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7948402/ https://www.ncbi.nlm.nih.gov/pubmed/33298525 http://dx.doi.org/10.1074/jbc.RA120.015876 |
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