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The transcript cleavage factor paralogue TFS4 is a potent RNA polymerase inhibitor

TFIIS-like transcript cleavage factors enhance the processivity and fidelity of archaeal and eukaryotic RNA polymerases. Sulfolobus solfataricus TFS1 functions as a bona fide cleavage factor, while the paralogous TFS4 evolved into a potent RNA polymerase inhibitor. TFS4 destabilises the TBP–TFB–RNAP...

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Autores principales: Fouqueau, Thomas, Blombach, Fabian, Hartman, Ross, Cheung, Alan C. M., Young, Mark J., Werner, Finn
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5715097/
https://www.ncbi.nlm.nih.gov/pubmed/29203770
http://dx.doi.org/10.1038/s41467-017-02081-3
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author Fouqueau, Thomas
Blombach, Fabian
Hartman, Ross
Cheung, Alan C. M.
Young, Mark J.
Werner, Finn
author_facet Fouqueau, Thomas
Blombach, Fabian
Hartman, Ross
Cheung, Alan C. M.
Young, Mark J.
Werner, Finn
author_sort Fouqueau, Thomas
collection PubMed
description TFIIS-like transcript cleavage factors enhance the processivity and fidelity of archaeal and eukaryotic RNA polymerases. Sulfolobus solfataricus TFS1 functions as a bona fide cleavage factor, while the paralogous TFS4 evolved into a potent RNA polymerase inhibitor. TFS4 destabilises the TBP–TFB–RNAP pre-initiation complex and inhibits transcription initiation and elongation. All inhibitory activities are dependent on three lysine residues at the tip of the C-terminal zinc ribbon of TFS4; the inhibition likely involves an allosteric component and is mitigated by the basal transcription factor TFEα/β. A chimeric variant of yeast TFIIS and TFS4 inhibits RNAPII transcription, suggesting that the molecular basis of inhibition is conserved between archaea and eukaryotes. TFS4 expression in S. solfataricus is induced in response to infection with the S ulfolobus turreted icosahedral virus. Our results reveal a compelling functional diversification of cleavage factors in archaea, and provide novel insights into transcription inhibition in the context of the host–virus relationship.
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spelling pubmed-57150972017-12-06 The transcript cleavage factor paralogue TFS4 is a potent RNA polymerase inhibitor Fouqueau, Thomas Blombach, Fabian Hartman, Ross Cheung, Alan C. M. Young, Mark J. Werner, Finn Nat Commun Article TFIIS-like transcript cleavage factors enhance the processivity and fidelity of archaeal and eukaryotic RNA polymerases. Sulfolobus solfataricus TFS1 functions as a bona fide cleavage factor, while the paralogous TFS4 evolved into a potent RNA polymerase inhibitor. TFS4 destabilises the TBP–TFB–RNAP pre-initiation complex and inhibits transcription initiation and elongation. All inhibitory activities are dependent on three lysine residues at the tip of the C-terminal zinc ribbon of TFS4; the inhibition likely involves an allosteric component and is mitigated by the basal transcription factor TFEα/β. A chimeric variant of yeast TFIIS and TFS4 inhibits RNAPII transcription, suggesting that the molecular basis of inhibition is conserved between archaea and eukaryotes. TFS4 expression in S. solfataricus is induced in response to infection with the S ulfolobus turreted icosahedral virus. Our results reveal a compelling functional diversification of cleavage factors in archaea, and provide novel insights into transcription inhibition in the context of the host–virus relationship. Nature Publishing Group UK 2017-12-04 /pmc/articles/PMC5715097/ /pubmed/29203770 http://dx.doi.org/10.1038/s41467-017-02081-3 Text en © The Author(s) 2017 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 Commonslicense, unless indicated otherwise in a credit line to the material. If material is not included in the article’sCreative 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/.
spellingShingle Article
Fouqueau, Thomas
Blombach, Fabian
Hartman, Ross
Cheung, Alan C. M.
Young, Mark J.
Werner, Finn
The transcript cleavage factor paralogue TFS4 is a potent RNA polymerase inhibitor
title The transcript cleavage factor paralogue TFS4 is a potent RNA polymerase inhibitor
title_full The transcript cleavage factor paralogue TFS4 is a potent RNA polymerase inhibitor
title_fullStr The transcript cleavage factor paralogue TFS4 is a potent RNA polymerase inhibitor
title_full_unstemmed The transcript cleavage factor paralogue TFS4 is a potent RNA polymerase inhibitor
title_short The transcript cleavage factor paralogue TFS4 is a potent RNA polymerase inhibitor
title_sort transcript cleavage factor paralogue tfs4 is a potent rna polymerase inhibitor
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5715097/
https://www.ncbi.nlm.nih.gov/pubmed/29203770
http://dx.doi.org/10.1038/s41467-017-02081-3
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