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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...

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Autores principales: Ren, Zhongqing, Liao, Qin, Karaboja, Xheni, Barton, Ian S., Schantz, Eli G., Mejia-Santana, Adrian, Fuqua, Clay, Wang, Xindan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2022
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.
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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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