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Positive supercoiling favors transcription elongation through lac repressor-mediated DNA loops
Some proteins, like the lac repressor (LacI), mediate long-range loops that alter DNA topology and create torsional barriers. During transcription, RNA polymerase generates supercoiling that may facilitate passage through such barriers. We monitored E. coli RNA polymerase progress along templates in...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8934669/ https://www.ncbi.nlm.nih.gov/pubmed/35188572 http://dx.doi.org/10.1093/nar/gkac093 |
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author | Xu, Wenxuan Yan, Yan Artsimovitch, Irina Dunlap, David Finzi, Laura |
author_facet | Xu, Wenxuan Yan, Yan Artsimovitch, Irina Dunlap, David Finzi, Laura |
author_sort | Xu, Wenxuan |
collection | PubMed |
description | Some proteins, like the lac repressor (LacI), mediate long-range loops that alter DNA topology and create torsional barriers. During transcription, RNA polymerase generates supercoiling that may facilitate passage through such barriers. We monitored E. coli RNA polymerase progress along templates in conditions that prevented, or favored, 400 bp LacI-mediated DNA looping. Tethered particle motion measurements revealed that RNA polymerase paused longer at unlooped LacI obstacles or those barring entry to a loop than those barring exit from the loop. Enhanced dissociation of a LacI roadblock by the positive supercoiling generated ahead of a transcribing RNA polymerase within a torsion-constrained DNA loop may be responsible for this reduction in pause time. In support of this idea, RNA polymerase transcribed 6-fold more slowly through looped DNA and paused at LacI obstacles for 66% less time on positively supercoiled compared to relaxed templates, especially under increased tension (torque). Positive supercoiling propagating ahead of polymerase facilitated elongation along topologically complex, protein-coated templates. |
format | Online Article Text |
id | pubmed-8934669 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-89346692022-03-21 Positive supercoiling favors transcription elongation through lac repressor-mediated DNA loops Xu, Wenxuan Yan, Yan Artsimovitch, Irina Dunlap, David Finzi, Laura Nucleic Acids Res Nucleic Acid Enzymes Some proteins, like the lac repressor (LacI), mediate long-range loops that alter DNA topology and create torsional barriers. During transcription, RNA polymerase generates supercoiling that may facilitate passage through such barriers. We monitored E. coli RNA polymerase progress along templates in conditions that prevented, or favored, 400 bp LacI-mediated DNA looping. Tethered particle motion measurements revealed that RNA polymerase paused longer at unlooped LacI obstacles or those barring entry to a loop than those barring exit from the loop. Enhanced dissociation of a LacI roadblock by the positive supercoiling generated ahead of a transcribing RNA polymerase within a torsion-constrained DNA loop may be responsible for this reduction in pause time. In support of this idea, RNA polymerase transcribed 6-fold more slowly through looped DNA and paused at LacI obstacles for 66% less time on positively supercoiled compared to relaxed templates, especially under increased tension (torque). Positive supercoiling propagating ahead of polymerase facilitated elongation along topologically complex, protein-coated templates. Oxford University Press 2022-02-21 /pmc/articles/PMC8934669/ /pubmed/35188572 http://dx.doi.org/10.1093/nar/gkac093 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of Nucleic Acids Research. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Nucleic Acid Enzymes Xu, Wenxuan Yan, Yan Artsimovitch, Irina Dunlap, David Finzi, Laura Positive supercoiling favors transcription elongation through lac repressor-mediated DNA loops |
title | Positive supercoiling favors transcription elongation through lac repressor-mediated DNA loops |
title_full | Positive supercoiling favors transcription elongation through lac repressor-mediated DNA loops |
title_fullStr | Positive supercoiling favors transcription elongation through lac repressor-mediated DNA loops |
title_full_unstemmed | Positive supercoiling favors transcription elongation through lac repressor-mediated DNA loops |
title_short | Positive supercoiling favors transcription elongation through lac repressor-mediated DNA loops |
title_sort | positive supercoiling favors transcription elongation through lac repressor-mediated dna loops |
topic | Nucleic Acid Enzymes |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8934669/ https://www.ncbi.nlm.nih.gov/pubmed/35188572 http://dx.doi.org/10.1093/nar/gkac093 |
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