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Conformation and dynamic interactions of the multipartite genome in Agrobacterium tumefaciens
Bacterial species from diverse phyla contain multiple replicons, yet how these multipartite genomes are organized and segregated during the cell cycle remains poorly understood. Agrobacterium tumefaciens has a 2.8-Mb circular chromosome (Ch1), a 2.1-Mb linear chromosome (Ch2), and two large plasmids...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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National Academy of Sciences
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8833148/ https://www.ncbi.nlm.nih.gov/pubmed/35101983 http://dx.doi.org/10.1073/pnas.2115854119 |
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author | Ren, Zhongqing Liao, Qin Karaboja, Xheni Barton, Ian S. Schantz, Eli G. Mejia-Santana, Adrian Fuqua, Clay Wang, Xindan |
author_facet | Ren, Zhongqing Liao, Qin Karaboja, Xheni Barton, Ian S. Schantz, Eli G. Mejia-Santana, Adrian Fuqua, Clay Wang, Xindan |
author_sort | Ren, Zhongqing |
collection | PubMed |
description | Bacterial species from diverse phyla contain multiple replicons, yet how these multipartite genomes are organized and segregated during the cell cycle remains poorly understood. Agrobacterium tumefaciens has a 2.8-Mb circular chromosome (Ch1), a 2.1-Mb linear chromosome (Ch2), and two large plasmids (pAt and pTi). We used this alpha proteobacterium as a model to investigate the global organization and temporal segregation of a multipartite genome. Using chromosome conformation capture assays, we demonstrate that both the circular and the linear chromosomes, but neither of the plasmids, have their left and right arms juxtaposed from their origins to their termini, generating interarm interactions that require the broadly conserved structural maintenance of chromosomes complex. Moreover, our study revealed two types of interreplicon interactions: “ori-ori clustering” in which the replication origins of all four replicons interact, and “Ch1-Ch2 alignment” in which the arms of Ch1 and Ch2 interact linearly along their lengths. We show that the centromeric proteins (ParB1 for Ch1 and RepB(Ch2) for Ch2) are required for both types of interreplicon contacts. Finally, using fluorescence microscopy, we validated the clustering of the origins and observed their frequent colocalization during segregation. Altogether, our findings provide a high-resolution view of the conformation of a multipartite genome. We hypothesize that intercentromeric contacts promote the organization and maintenance of diverse replicons. |
format | Online Article Text |
id | pubmed-8833148 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | National Academy of Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-88331482022-07-31 Conformation and dynamic interactions of the multipartite genome in Agrobacterium tumefaciens Ren, Zhongqing Liao, Qin Karaboja, Xheni Barton, Ian S. Schantz, Eli G. Mejia-Santana, Adrian Fuqua, Clay Wang, Xindan Proc Natl Acad Sci U S A Biological Sciences Bacterial species from diverse phyla contain multiple replicons, yet how these multipartite genomes are organized and segregated during the cell cycle remains poorly understood. Agrobacterium tumefaciens has a 2.8-Mb circular chromosome (Ch1), a 2.1-Mb linear chromosome (Ch2), and two large plasmids (pAt and pTi). We used this alpha proteobacterium as a model to investigate the global organization and temporal segregation of a multipartite genome. Using chromosome conformation capture assays, we demonstrate that both the circular and the linear chromosomes, but neither of the plasmids, have their left and right arms juxtaposed from their origins to their termini, generating interarm interactions that require the broadly conserved structural maintenance of chromosomes complex. Moreover, our study revealed two types of interreplicon interactions: “ori-ori clustering” in which the replication origins of all four replicons interact, and “Ch1-Ch2 alignment” in which the arms of Ch1 and Ch2 interact linearly along their lengths. We show that the centromeric proteins (ParB1 for Ch1 and RepB(Ch2) for Ch2) are required for both types of interreplicon contacts. Finally, using fluorescence microscopy, we validated the clustering of the origins and observed their frequent colocalization during segregation. Altogether, our findings provide a high-resolution view of the conformation of a multipartite genome. We hypothesize that intercentromeric contacts promote the organization and maintenance of diverse replicons. National Academy of Sciences 2022-01-31 2022-02-08 /pmc/articles/PMC8833148/ /pubmed/35101983 http://dx.doi.org/10.1073/pnas.2115854119 Text en Copyright © 2022 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/This article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) . |
spellingShingle | Biological Sciences Ren, Zhongqing Liao, Qin Karaboja, Xheni Barton, Ian S. Schantz, Eli G. Mejia-Santana, Adrian Fuqua, Clay Wang, Xindan Conformation and dynamic interactions of the multipartite genome in Agrobacterium tumefaciens |
title | Conformation and dynamic interactions of the multipartite genome in Agrobacterium tumefaciens |
title_full | Conformation and dynamic interactions of the multipartite genome in Agrobacterium tumefaciens |
title_fullStr | Conformation and dynamic interactions of the multipartite genome in Agrobacterium tumefaciens |
title_full_unstemmed | Conformation and dynamic interactions of the multipartite genome in Agrobacterium tumefaciens |
title_short | Conformation and dynamic interactions of the multipartite genome in Agrobacterium tumefaciens |
title_sort | conformation and dynamic interactions of the multipartite genome in agrobacterium tumefaciens |
topic | Biological Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8833148/ https://www.ncbi.nlm.nih.gov/pubmed/35101983 http://dx.doi.org/10.1073/pnas.2115854119 |
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