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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...

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Autores principales: Blombach, Fabian, Fouqueau, Thomas, Matelska, Dorota, Smollett, Katherine, Werner, Finn
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
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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.
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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
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