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Organization and replicon interactions within the highly segmented genome of Borrelia burgdorferi

Borrelia burgdorferi, a causative agent of Lyme disease, contains the most segmented bacterial genome known to date, with one linear chromosome and over twenty plasmids. How this unusually complex genome is organized, and whether and how the different replicons interact are unclear. We recently demo...

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Autores principales: Ren, Zhongqing, Takacs, Constantin N., Brandão, Hugo B., Jacobs-Wagner, Christine, Wang, Xindan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10103936/
https://www.ncbi.nlm.nih.gov/pubmed/37066390
http://dx.doi.org/10.1101/2023.03.19.532819
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author Ren, Zhongqing
Takacs, Constantin N.
Brandão, Hugo B.
Jacobs-Wagner, Christine
Wang, Xindan
author_facet Ren, Zhongqing
Takacs, Constantin N.
Brandão, Hugo B.
Jacobs-Wagner, Christine
Wang, Xindan
author_sort Ren, Zhongqing
collection PubMed
description Borrelia burgdorferi, a causative agent of Lyme disease, contains the most segmented bacterial genome known to date, with one linear chromosome and over twenty plasmids. How this unusually complex genome is organized, and whether and how the different replicons interact are unclear. We recently demonstrated that B. burgdorferi is polyploid and that the copies of the chromosome and plasmids are regularly spaced in each cell, which is critical for faithful segregation of the genome to daughter cells. Regular spacing of the chromosome is controlled by two separate partitioning systems that involve the protein pairs ParA/ParZ and ParB/SMC. Here, using chromosome conformation capture (Hi-C), we characterized the organization of the B. burgdorferi genome and the interactions between the replicons. We uncovered that although the linear chromosome lacks contacts between the two replication arms, the two telomeres are in frequent contact. Moreover, several plasmids specifically interact with the chromosome oriC region, and a subset of plasmids interact with each other more than with others. We found that SMC and the SMC-like MksB protein mediate long-range interactions on the chromosome, but they minimally affect plasmid-chromosome or plasmid-plasmid interactions. Finally, we found that disruption of the two partition systems leads to chromosome restructuring, correlating with the mis-positioning of chromosome oriC. Altogether, this study revealed the conformation of a complex genome and analyzed the contribution of the partition systems and SMC family proteins to this organization. This work expands the understanding of the organization and maintenance of multipartite bacterial genomes.
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spelling pubmed-101039362023-04-15 Organization and replicon interactions within the highly segmented genome of Borrelia burgdorferi Ren, Zhongqing Takacs, Constantin N. Brandão, Hugo B. Jacobs-Wagner, Christine Wang, Xindan bioRxiv Article Borrelia burgdorferi, a causative agent of Lyme disease, contains the most segmented bacterial genome known to date, with one linear chromosome and over twenty plasmids. How this unusually complex genome is organized, and whether and how the different replicons interact are unclear. We recently demonstrated that B. burgdorferi is polyploid and that the copies of the chromosome and plasmids are regularly spaced in each cell, which is critical for faithful segregation of the genome to daughter cells. Regular spacing of the chromosome is controlled by two separate partitioning systems that involve the protein pairs ParA/ParZ and ParB/SMC. Here, using chromosome conformation capture (Hi-C), we characterized the organization of the B. burgdorferi genome and the interactions between the replicons. We uncovered that although the linear chromosome lacks contacts between the two replication arms, the two telomeres are in frequent contact. Moreover, several plasmids specifically interact with the chromosome oriC region, and a subset of plasmids interact with each other more than with others. We found that SMC and the SMC-like MksB protein mediate long-range interactions on the chromosome, but they minimally affect plasmid-chromosome or plasmid-plasmid interactions. Finally, we found that disruption of the two partition systems leads to chromosome restructuring, correlating with the mis-positioning of chromosome oriC. Altogether, this study revealed the conformation of a complex genome and analyzed the contribution of the partition systems and SMC family proteins to this organization. This work expands the understanding of the organization and maintenance of multipartite bacterial genomes. Cold Spring Harbor Laboratory 2023-04-05 /pmc/articles/PMC10103936/ /pubmed/37066390 http://dx.doi.org/10.1101/2023.03.19.532819 Text en https://creativecommons.org/licenses/by-nc/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License (https://creativecommons.org/licenses/by-nc/4.0/) , which allows reusers to distribute, remix, adapt, and build upon the material in any medium or format for noncommercial purposes only, and only so long as attribution is given to the creator.
spellingShingle Article
Ren, Zhongqing
Takacs, Constantin N.
Brandão, Hugo B.
Jacobs-Wagner, Christine
Wang, Xindan
Organization and replicon interactions within the highly segmented genome of Borrelia burgdorferi
title Organization and replicon interactions within the highly segmented genome of Borrelia burgdorferi
title_full Organization and replicon interactions within the highly segmented genome of Borrelia burgdorferi
title_fullStr Organization and replicon interactions within the highly segmented genome of Borrelia burgdorferi
title_full_unstemmed Organization and replicon interactions within the highly segmented genome of Borrelia burgdorferi
title_short Organization and replicon interactions within the highly segmented genome of Borrelia burgdorferi
title_sort organization and replicon interactions within the highly segmented genome of borrelia burgdorferi
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10103936/
https://www.ncbi.nlm.nih.gov/pubmed/37066390
http://dx.doi.org/10.1101/2023.03.19.532819
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