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Psoralen mapping reveals a bacterial genome supercoiling landscape dominated by transcription
DNA supercoiling is a key regulator of all DNA metabolic processes including replication, transcription, and recombination, yet a reliable genomic assay for supercoiling is lacking. Here, we present a robust and flexible method (Psora-seq) to measure whole-genome supercoiling at high resolution. Usi...
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/PMC9071471/ https://www.ncbi.nlm.nih.gov/pubmed/35420137 http://dx.doi.org/10.1093/nar/gkac244 |
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author | Visser, Bryan J Sharma, Sonum Chen, Po J McMullin, Anna B Bates, Maia L Bates, David |
author_facet | Visser, Bryan J Sharma, Sonum Chen, Po J McMullin, Anna B Bates, Maia L Bates, David |
author_sort | Visser, Bryan J |
collection | PubMed |
description | DNA supercoiling is a key regulator of all DNA metabolic processes including replication, transcription, and recombination, yet a reliable genomic assay for supercoiling is lacking. Here, we present a robust and flexible method (Psora-seq) to measure whole-genome supercoiling at high resolution. Using this tool in Escherichia coli, we observe a supercoiling landscape that is well correlated to transcription. Supercoiling twin-domains generated by RNA polymerase complexes span 25 kb in each direction – an order of magnitude farther than previous measurements in any organism. Thus, ribosomal and many other highly expressed genes strongly affect the topology of about 40 neighboring genes each, creating highly integrated gene circuits. Genomic patterns of supercoiling revealed by Psora-seq could be aptly predicted from modeling based on gene expression levels alone, indicating that transcription is the major determinant of chromosome supercoiling. Large-scale supercoiling patterns were highly symmetrical between left and right chromosome arms (replichores), indicating that DNA replication also strongly influences supercoiling. Skew in the axis of symmetry from the natural ori-ter axis supports previous indications that the rightward replication fork is delayed several minutes after initiation. Implications of supercoiling on DNA replication and chromosome domain structure are discussed. |
format | Online Article Text |
id | pubmed-9071471 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-90714712022-05-06 Psoralen mapping reveals a bacterial genome supercoiling landscape dominated by transcription Visser, Bryan J Sharma, Sonum Chen, Po J McMullin, Anna B Bates, Maia L Bates, David Nucleic Acids Res Gene regulation, Chromatin and Epigenetics DNA supercoiling is a key regulator of all DNA metabolic processes including replication, transcription, and recombination, yet a reliable genomic assay for supercoiling is lacking. Here, we present a robust and flexible method (Psora-seq) to measure whole-genome supercoiling at high resolution. Using this tool in Escherichia coli, we observe a supercoiling landscape that is well correlated to transcription. Supercoiling twin-domains generated by RNA polymerase complexes span 25 kb in each direction – an order of magnitude farther than previous measurements in any organism. Thus, ribosomal and many other highly expressed genes strongly affect the topology of about 40 neighboring genes each, creating highly integrated gene circuits. Genomic patterns of supercoiling revealed by Psora-seq could be aptly predicted from modeling based on gene expression levels alone, indicating that transcription is the major determinant of chromosome supercoiling. Large-scale supercoiling patterns were highly symmetrical between left and right chromosome arms (replichores), indicating that DNA replication also strongly influences supercoiling. Skew in the axis of symmetry from the natural ori-ter axis supports previous indications that the rightward replication fork is delayed several minutes after initiation. Implications of supercoiling on DNA replication and chromosome domain structure are discussed. Oxford University Press 2022-04-14 /pmc/articles/PMC9071471/ /pubmed/35420137 http://dx.doi.org/10.1093/nar/gkac244 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of Nucleic Acids Research. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Gene regulation, Chromatin and Epigenetics Visser, Bryan J Sharma, Sonum Chen, Po J McMullin, Anna B Bates, Maia L Bates, David Psoralen mapping reveals a bacterial genome supercoiling landscape dominated by transcription |
title | Psoralen mapping reveals a bacterial genome supercoiling landscape dominated by transcription |
title_full | Psoralen mapping reveals a bacterial genome supercoiling landscape dominated by transcription |
title_fullStr | Psoralen mapping reveals a bacterial genome supercoiling landscape dominated by transcription |
title_full_unstemmed | Psoralen mapping reveals a bacterial genome supercoiling landscape dominated by transcription |
title_short | Psoralen mapping reveals a bacterial genome supercoiling landscape dominated by transcription |
title_sort | psoralen mapping reveals a bacterial genome supercoiling landscape dominated by transcription |
topic | Gene regulation, Chromatin and Epigenetics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9071471/ https://www.ncbi.nlm.nih.gov/pubmed/35420137 http://dx.doi.org/10.1093/nar/gkac244 |
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