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The universally-conserved transcription factor RfaH is recruited to a hairpin structure of the non-template DNA strand
RfaH, a transcription regulator of the universally conserved NusG/Spt5 family, utilizes a unique mode of recruitment to elongating RNA polymerase to activate virulence genes. RfaH function depends critically on an ops sequence, an exemplar of a consensus pause, in the non-template DNA strand of the...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5995543/ https://www.ncbi.nlm.nih.gov/pubmed/29741479 http://dx.doi.org/10.7554/eLife.36349 |
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author | Zuber, Philipp K Artsimovitch, Irina NandyMazumdar, Monali Liu, Zhaokun Nedialkov, Yuri Schweimer, Kristian Rösch, Paul Knauer, Stefan H |
author_facet | Zuber, Philipp K Artsimovitch, Irina NandyMazumdar, Monali Liu, Zhaokun Nedialkov, Yuri Schweimer, Kristian Rösch, Paul Knauer, Stefan H |
author_sort | Zuber, Philipp K |
collection | PubMed |
description | RfaH, a transcription regulator of the universally conserved NusG/Spt5 family, utilizes a unique mode of recruitment to elongating RNA polymerase to activate virulence genes. RfaH function depends critically on an ops sequence, an exemplar of a consensus pause, in the non-template DNA strand of the transcription bubble. We used structural and functional analyses to elucidate the role of ops in RfaH recruitment. Our results demonstrate that ops induces pausing to facilitate RfaH binding and establishes direct contacts with RfaH. Strikingly, the non-template DNA forms a hairpin in the RfaH:ops complex structure, flipping out a conserved T residue that is specifically recognized by RfaH. Molecular modeling and genetic evidence support the notion that ops hairpin is required for RfaH recruitment. We argue that both the sequence and the structure of the non-template strand are read out by transcription factors, expanding the repertoire of transcriptional regulators in all domains of life. |
format | Online Article Text |
id | pubmed-5995543 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-59955432018-06-13 The universally-conserved transcription factor RfaH is recruited to a hairpin structure of the non-template DNA strand Zuber, Philipp K Artsimovitch, Irina NandyMazumdar, Monali Liu, Zhaokun Nedialkov, Yuri Schweimer, Kristian Rösch, Paul Knauer, Stefan H eLife Biochemistry and Chemical Biology RfaH, a transcription regulator of the universally conserved NusG/Spt5 family, utilizes a unique mode of recruitment to elongating RNA polymerase to activate virulence genes. RfaH function depends critically on an ops sequence, an exemplar of a consensus pause, in the non-template DNA strand of the transcription bubble. We used structural and functional analyses to elucidate the role of ops in RfaH recruitment. Our results demonstrate that ops induces pausing to facilitate RfaH binding and establishes direct contacts with RfaH. Strikingly, the non-template DNA forms a hairpin in the RfaH:ops complex structure, flipping out a conserved T residue that is specifically recognized by RfaH. Molecular modeling and genetic evidence support the notion that ops hairpin is required for RfaH recruitment. We argue that both the sequence and the structure of the non-template strand are read out by transcription factors, expanding the repertoire of transcriptional regulators in all domains of life. eLife Sciences Publications, Ltd 2018-05-09 /pmc/articles/PMC5995543/ /pubmed/29741479 http://dx.doi.org/10.7554/eLife.36349 Text en © 2018, Zuber et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Biochemistry and Chemical Biology Zuber, Philipp K Artsimovitch, Irina NandyMazumdar, Monali Liu, Zhaokun Nedialkov, Yuri Schweimer, Kristian Rösch, Paul Knauer, Stefan H The universally-conserved transcription factor RfaH is recruited to a hairpin structure of the non-template DNA strand |
title | The universally-conserved transcription factor RfaH is recruited to a hairpin structure of the non-template DNA strand |
title_full | The universally-conserved transcription factor RfaH is recruited to a hairpin structure of the non-template DNA strand |
title_fullStr | The universally-conserved transcription factor RfaH is recruited to a hairpin structure of the non-template DNA strand |
title_full_unstemmed | The universally-conserved transcription factor RfaH is recruited to a hairpin structure of the non-template DNA strand |
title_short | The universally-conserved transcription factor RfaH is recruited to a hairpin structure of the non-template DNA strand |
title_sort | universally-conserved transcription factor rfah is recruited to a hairpin structure of the non-template dna strand |
topic | Biochemistry and Chemical Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5995543/ https://www.ncbi.nlm.nih.gov/pubmed/29741479 http://dx.doi.org/10.7554/eLife.36349 |
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