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DNA Supercoiling Drives a Transition between Collective Modes of Gene Synthesis

Transcription of genes can be affected by both biochemical and mechanical factors. Recent experiments suggested that the mechanical stress associated with transcription-induced DNA supercoiling is responsible for the transition from cooperative to antagonistic group dynamics of RNA polymerases (RNAP...

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Autores principales: Chatterjee, Purba, Goldenfeld, Nigel, Kim, Sangjin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9034659/
https://www.ncbi.nlm.nih.gov/pubmed/34860091
http://dx.doi.org/10.1103/PhysRevLett.127.218101
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author Chatterjee, Purba
Goldenfeld, Nigel
Kim, Sangjin
author_facet Chatterjee, Purba
Goldenfeld, Nigel
Kim, Sangjin
author_sort Chatterjee, Purba
collection PubMed
description Transcription of genes can be affected by both biochemical and mechanical factors. Recent experiments suggested that the mechanical stress associated with transcription-induced DNA supercoiling is responsible for the transition from cooperative to antagonistic group dynamics of RNA polymerases (RNAPs) upon promoter repression. To underpin the mechanism behind this drastic transition, we developed a continuum deterministic model for transcription under torsion. In our model, the speed of an RNAP is affected by the local DNA supercoiling, as well as two global factors: (i) the number of RNAPs on the gene affecting the torsional stress experienced by individual RNAPs and (ii) transcription factors blocking the diffusion of DNA supercoils. Our minimal model can successfully reproduce the experimental findings and helps elucidate the interplay of mechanical and biological factors in the collective dynamics of molecular machines involved in gene expression.
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spelling pubmed-90346592022-04-23 DNA Supercoiling Drives a Transition between Collective Modes of Gene Synthesis Chatterjee, Purba Goldenfeld, Nigel Kim, Sangjin Phys Rev Lett Article Transcription of genes can be affected by both biochemical and mechanical factors. Recent experiments suggested that the mechanical stress associated with transcription-induced DNA supercoiling is responsible for the transition from cooperative to antagonistic group dynamics of RNA polymerases (RNAPs) upon promoter repression. To underpin the mechanism behind this drastic transition, we developed a continuum deterministic model for transcription under torsion. In our model, the speed of an RNAP is affected by the local DNA supercoiling, as well as two global factors: (i) the number of RNAPs on the gene affecting the torsional stress experienced by individual RNAPs and (ii) transcription factors blocking the diffusion of DNA supercoils. Our minimal model can successfully reproduce the experimental findings and helps elucidate the interplay of mechanical and biological factors in the collective dynamics of molecular machines involved in gene expression. 2021-11-19 /pmc/articles/PMC9034659/ /pubmed/34860091 http://dx.doi.org/10.1103/PhysRevLett.127.218101 Text en https://creativecommons.org/licenses/by/4.0/Published by the American Physical Society under the terms of the Creative Commons Attribution 4.0 International (https://creativecommons.org/licenses/by/4.0/) license. Further distribution of this work must maintain attribution to the author(s) and the published article’s title, journal citation, and DOI.
spellingShingle Article
Chatterjee, Purba
Goldenfeld, Nigel
Kim, Sangjin
DNA Supercoiling Drives a Transition between Collective Modes of Gene Synthesis
title DNA Supercoiling Drives a Transition between Collective Modes of Gene Synthesis
title_full DNA Supercoiling Drives a Transition between Collective Modes of Gene Synthesis
title_fullStr DNA Supercoiling Drives a Transition between Collective Modes of Gene Synthesis
title_full_unstemmed DNA Supercoiling Drives a Transition between Collective Modes of Gene Synthesis
title_short DNA Supercoiling Drives a Transition between Collective Modes of Gene Synthesis
title_sort dna supercoiling drives a transition between collective modes of gene synthesis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9034659/
https://www.ncbi.nlm.nih.gov/pubmed/34860091
http://dx.doi.org/10.1103/PhysRevLett.127.218101
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