Cargando…
Complex polar machinery required for proper chromosome segregation in vegetative and sporulating cells of Bacillus subtilis
Chromosome segregation is an essential process of cell multiplication. In prokaryotes, segregation starts with the newly replicated sister origins of replication, oriCs, which move apart to defined positions in the cell. We have developed a genetic screen to identify mutants defective in placement o...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4949633/ https://www.ncbi.nlm.nih.gov/pubmed/27059541 http://dx.doi.org/10.1111/mmi.13393 |
_version_ | 1782443464638595072 |
---|---|
author | Kloosterman, Tomas G. Lenarcic, Rok Willis, Clare R. Roberts, David M. Hamoen, Leendert W. Errington, Jeff Wu, Ling J. |
author_facet | Kloosterman, Tomas G. Lenarcic, Rok Willis, Clare R. Roberts, David M. Hamoen, Leendert W. Errington, Jeff Wu, Ling J. |
author_sort | Kloosterman, Tomas G. |
collection | PubMed |
description | Chromosome segregation is an essential process of cell multiplication. In prokaryotes, segregation starts with the newly replicated sister origins of replication, oriCs, which move apart to defined positions in the cell. We have developed a genetic screen to identify mutants defective in placement of oriC during spore development in the Gram‐positive bacterium Bacillus subtilis. In addition to the previously identified proteins Soj and DivIVA, our screen identified several new factors involved in polar recruitment of oriC: a reported regulator of competence ComN, and the regulators of division site selection MinD and MinJ. Previous work implicated Soj as an important regulator of oriC positioning in the cell. Our results suggest a model in which the DivIVA‐interacting proteins ComN and MinJ recruit MinD to the cell pole, and that these proteins work upstream of Soj to enable oriC placement. We show that these proteins form a polar complex, which acts in parallel with but distinct from the sporulation‐specific RacA pathway of oriC placement, and also functions during vegetative growth. Our study further shows that MinD has two distinct cell cycle roles, in cell division and chromosome segregation, and highlights that cell probably use multiple parallel mechanisms to ensure accurate chromosome segregation. |
format | Online Article Text |
id | pubmed-4949633 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-49496332016-08-05 Complex polar machinery required for proper chromosome segregation in vegetative and sporulating cells of Bacillus subtilis Kloosterman, Tomas G. Lenarcic, Rok Willis, Clare R. Roberts, David M. Hamoen, Leendert W. Errington, Jeff Wu, Ling J. Mol Microbiol Research Articles Chromosome segregation is an essential process of cell multiplication. In prokaryotes, segregation starts with the newly replicated sister origins of replication, oriCs, which move apart to defined positions in the cell. We have developed a genetic screen to identify mutants defective in placement of oriC during spore development in the Gram‐positive bacterium Bacillus subtilis. In addition to the previously identified proteins Soj and DivIVA, our screen identified several new factors involved in polar recruitment of oriC: a reported regulator of competence ComN, and the regulators of division site selection MinD and MinJ. Previous work implicated Soj as an important regulator of oriC positioning in the cell. Our results suggest a model in which the DivIVA‐interacting proteins ComN and MinJ recruit MinD to the cell pole, and that these proteins work upstream of Soj to enable oriC placement. We show that these proteins form a polar complex, which acts in parallel with but distinct from the sporulation‐specific RacA pathway of oriC placement, and also functions during vegetative growth. Our study further shows that MinD has two distinct cell cycle roles, in cell division and chromosome segregation, and highlights that cell probably use multiple parallel mechanisms to ensure accurate chromosome segregation. John Wiley and Sons Inc. 2016-05-18 2016-07 /pmc/articles/PMC4949633/ /pubmed/27059541 http://dx.doi.org/10.1111/mmi.13393 Text en © 2016 The Authors. Molecular Microbiology Published by John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Kloosterman, Tomas G. Lenarcic, Rok Willis, Clare R. Roberts, David M. Hamoen, Leendert W. Errington, Jeff Wu, Ling J. Complex polar machinery required for proper chromosome segregation in vegetative and sporulating cells of Bacillus subtilis |
title | Complex polar machinery required for proper chromosome segregation in vegetative and sporulating cells of Bacillus subtilis
|
title_full | Complex polar machinery required for proper chromosome segregation in vegetative and sporulating cells of Bacillus subtilis
|
title_fullStr | Complex polar machinery required for proper chromosome segregation in vegetative and sporulating cells of Bacillus subtilis
|
title_full_unstemmed | Complex polar machinery required for proper chromosome segregation in vegetative and sporulating cells of Bacillus subtilis
|
title_short | Complex polar machinery required for proper chromosome segregation in vegetative and sporulating cells of Bacillus subtilis
|
title_sort | complex polar machinery required for proper chromosome segregation in vegetative and sporulating cells of bacillus subtilis |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4949633/ https://www.ncbi.nlm.nih.gov/pubmed/27059541 http://dx.doi.org/10.1111/mmi.13393 |
work_keys_str_mv | AT kloostermantomasg complexpolarmachineryrequiredforproperchromosomesegregationinvegetativeandsporulatingcellsofbacillussubtilis AT lenarcicrok complexpolarmachineryrequiredforproperchromosomesegregationinvegetativeandsporulatingcellsofbacillussubtilis AT willisclarer complexpolarmachineryrequiredforproperchromosomesegregationinvegetativeandsporulatingcellsofbacillussubtilis AT robertsdavidm complexpolarmachineryrequiredforproperchromosomesegregationinvegetativeandsporulatingcellsofbacillussubtilis AT hamoenleendertw complexpolarmachineryrequiredforproperchromosomesegregationinvegetativeandsporulatingcellsofbacillussubtilis AT erringtonjeff complexpolarmachineryrequiredforproperchromosomesegregationinvegetativeandsporulatingcellsofbacillussubtilis AT wulingj complexpolarmachineryrequiredforproperchromosomesegregationinvegetativeandsporulatingcellsofbacillussubtilis |