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Synchronous termination of replication of the two chromosomes is an evolutionary selected feature in Vibrionaceae
Vibrio cholerae, the causative agent of the cholera disease, is commonly used as a model organism for the study of bacteria with multipartite genomes. Its two chromosomes of different sizes initiate their DNA replication at distinct time points in the cell cycle and terminate in synchrony. In this s...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5854411/ https://www.ncbi.nlm.nih.gov/pubmed/29505558 http://dx.doi.org/10.1371/journal.pgen.1007251 |
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author | Kemter, Franziska S. Messerschmidt, Sonja J. Schallopp, Nadine Sobetzko, Patrick Lang, Elke Bunk, Boyke Spröer, Cathrin Teschler, Jennifer K. Yildiz, Fitnat H. Overmann, Jörg Waldminghaus, Torsten |
author_facet | Kemter, Franziska S. Messerschmidt, Sonja J. Schallopp, Nadine Sobetzko, Patrick Lang, Elke Bunk, Boyke Spröer, Cathrin Teschler, Jennifer K. Yildiz, Fitnat H. Overmann, Jörg Waldminghaus, Torsten |
author_sort | Kemter, Franziska S. |
collection | PubMed |
description | Vibrio cholerae, the causative agent of the cholera disease, is commonly used as a model organism for the study of bacteria with multipartite genomes. Its two chromosomes of different sizes initiate their DNA replication at distinct time points in the cell cycle and terminate in synchrony. In this study, the time-delayed start of Chr2 was verified in a synchronized cell population. This replication pattern suggests two possible regulation mechanisms for other Vibrio species with different sized secondary chromosomes: Either all Chr2 start DNA replication with a fixed delay after Chr1 initiation, or the timepoint at which Chr2 initiates varies such that termination of chromosomal replication occurs in synchrony. We investigated these two models and revealed that the two chromosomes of various Vibrionaceae species terminate in synchrony while Chr2-initiation timing relative to Chr1 is variable. Moreover, the sequence and function of the Chr2-triggering crtS site recently discovered in V. cholerae were found to be conserved, explaining the observed timing mechanism. Our results suggest that it is beneficial for bacterial cells with multiple chromosomes to synchronize their replication termination, potentially to optimize chromosome related processes as dimer resolution or segregation. |
format | Online Article Text |
id | pubmed-5854411 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-58544112018-03-28 Synchronous termination of replication of the two chromosomes is an evolutionary selected feature in Vibrionaceae Kemter, Franziska S. Messerschmidt, Sonja J. Schallopp, Nadine Sobetzko, Patrick Lang, Elke Bunk, Boyke Spröer, Cathrin Teschler, Jennifer K. Yildiz, Fitnat H. Overmann, Jörg Waldminghaus, Torsten PLoS Genet Research Article Vibrio cholerae, the causative agent of the cholera disease, is commonly used as a model organism for the study of bacteria with multipartite genomes. Its two chromosomes of different sizes initiate their DNA replication at distinct time points in the cell cycle and terminate in synchrony. In this study, the time-delayed start of Chr2 was verified in a synchronized cell population. This replication pattern suggests two possible regulation mechanisms for other Vibrio species with different sized secondary chromosomes: Either all Chr2 start DNA replication with a fixed delay after Chr1 initiation, or the timepoint at which Chr2 initiates varies such that termination of chromosomal replication occurs in synchrony. We investigated these two models and revealed that the two chromosomes of various Vibrionaceae species terminate in synchrony while Chr2-initiation timing relative to Chr1 is variable. Moreover, the sequence and function of the Chr2-triggering crtS site recently discovered in V. cholerae were found to be conserved, explaining the observed timing mechanism. Our results suggest that it is beneficial for bacterial cells with multiple chromosomes to synchronize their replication termination, potentially to optimize chromosome related processes as dimer resolution or segregation. Public Library of Science 2018-03-05 /pmc/articles/PMC5854411/ /pubmed/29505558 http://dx.doi.org/10.1371/journal.pgen.1007251 Text en © 2018 Kemter et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Kemter, Franziska S. Messerschmidt, Sonja J. Schallopp, Nadine Sobetzko, Patrick Lang, Elke Bunk, Boyke Spröer, Cathrin Teschler, Jennifer K. Yildiz, Fitnat H. Overmann, Jörg Waldminghaus, Torsten Synchronous termination of replication of the two chromosomes is an evolutionary selected feature in Vibrionaceae |
title | Synchronous termination of replication of the two chromosomes is an evolutionary selected feature in Vibrionaceae |
title_full | Synchronous termination of replication of the two chromosomes is an evolutionary selected feature in Vibrionaceae |
title_fullStr | Synchronous termination of replication of the two chromosomes is an evolutionary selected feature in Vibrionaceae |
title_full_unstemmed | Synchronous termination of replication of the two chromosomes is an evolutionary selected feature in Vibrionaceae |
title_short | Synchronous termination of replication of the two chromosomes is an evolutionary selected feature in Vibrionaceae |
title_sort | synchronous termination of replication of the two chromosomes is an evolutionary selected feature in vibrionaceae |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5854411/ https://www.ncbi.nlm.nih.gov/pubmed/29505558 http://dx.doi.org/10.1371/journal.pgen.1007251 |
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