Cargando…
Promoter-proximal elongation regulates transcription in archaea
Recruitment of RNA polymerase and initiation factors to the promoter is the only known target for transcription activation and repression in archaea. Whether any of the subsequent steps towards productive transcription elongation are involved in regulation is not known. We characterised how the basa...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8448881/ https://www.ncbi.nlm.nih.gov/pubmed/34535658 http://dx.doi.org/10.1038/s41467-021-25669-2 |
_version_ | 1784569331222315008 |
---|---|
author | Blombach, Fabian Fouqueau, Thomas Matelska, Dorota Smollett, Katherine Werner, Finn |
author_facet | Blombach, Fabian Fouqueau, Thomas Matelska, Dorota Smollett, Katherine Werner, Finn |
author_sort | Blombach, Fabian |
collection | PubMed |
description | Recruitment of RNA polymerase and initiation factors to the promoter is the only known target for transcription activation and repression in archaea. Whether any of the subsequent steps towards productive transcription elongation are involved in regulation is not known. We characterised how the basal transcription machinery is distributed along genes in the archaeon Saccharolobus solfataricus. We discovered a distinct early elongation phase where RNA polymerases sequentially recruit the elongation factors Spt4/5 and Elf1 to form the transcription elongation complex (TEC) before the TEC escapes into productive transcription. TEC escape is rate-limiting for transcription output during exponential growth. Oxidative stress causes changes in TEC escape that correlate with changes in the transcriptome. Our results thus establish that TEC escape contributes to the basal promoter strength and facilitates transcription regulation. Impaired TEC escape coincides with the accumulation of initiation factors at the promoter and recruitment of termination factor aCPSF1 to the early TEC. This suggests two possible mechanisms for how TEC escape limits transcription, physically blocking upstream RNA polymerases during transcription initiation and premature termination of early TECs. |
format | Online Article Text |
id | pubmed-8448881 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-84488812021-10-05 Promoter-proximal elongation regulates transcription in archaea Blombach, Fabian Fouqueau, Thomas Matelska, Dorota Smollett, Katherine Werner, Finn Nat Commun Article Recruitment of RNA polymerase and initiation factors to the promoter is the only known target for transcription activation and repression in archaea. Whether any of the subsequent steps towards productive transcription elongation are involved in regulation is not known. We characterised how the basal transcription machinery is distributed along genes in the archaeon Saccharolobus solfataricus. We discovered a distinct early elongation phase where RNA polymerases sequentially recruit the elongation factors Spt4/5 and Elf1 to form the transcription elongation complex (TEC) before the TEC escapes into productive transcription. TEC escape is rate-limiting for transcription output during exponential growth. Oxidative stress causes changes in TEC escape that correlate with changes in the transcriptome. Our results thus establish that TEC escape contributes to the basal promoter strength and facilitates transcription regulation. Impaired TEC escape coincides with the accumulation of initiation factors at the promoter and recruitment of termination factor aCPSF1 to the early TEC. This suggests two possible mechanisms for how TEC escape limits transcription, physically blocking upstream RNA polymerases during transcription initiation and premature termination of early TECs. Nature Publishing Group UK 2021-09-17 /pmc/articles/PMC8448881/ /pubmed/34535658 http://dx.doi.org/10.1038/s41467-021-25669-2 Text en © Crown 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Blombach, Fabian Fouqueau, Thomas Matelska, Dorota Smollett, Katherine Werner, Finn Promoter-proximal elongation regulates transcription in archaea |
title | Promoter-proximal elongation regulates transcription in archaea |
title_full | Promoter-proximal elongation regulates transcription in archaea |
title_fullStr | Promoter-proximal elongation regulates transcription in archaea |
title_full_unstemmed | Promoter-proximal elongation regulates transcription in archaea |
title_short | Promoter-proximal elongation regulates transcription in archaea |
title_sort | promoter-proximal elongation regulates transcription in archaea |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8448881/ https://www.ncbi.nlm.nih.gov/pubmed/34535658 http://dx.doi.org/10.1038/s41467-021-25669-2 |
work_keys_str_mv | AT blombachfabian promoterproximalelongationregulatestranscriptioninarchaea AT fouqueauthomas promoterproximalelongationregulatestranscriptioninarchaea AT matelskadorota promoterproximalelongationregulatestranscriptioninarchaea AT smollettkatherine promoterproximalelongationregulatestranscriptioninarchaea AT wernerfinn promoterproximalelongationregulatestranscriptioninarchaea |