Cargando…
HdaB: a novel and conserved DnaA-related protein that targets the RIDA process to stimulate replication initiation
Exquisite control of the DnaA initiator is critical to ensure that bacteria initiate chromosome replication in a cell cycle-coordinated manner. In many bacteria, the DnaA-related and replisome-associated Hda/HdaA protein interacts with DnaA to trigger the Regulatory Inactivation of DnaA (RIDA) and p...
Autores principales: | , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7049699/ https://www.ncbi.nlm.nih.gov/pubmed/31875223 http://dx.doi.org/10.1093/nar/gkz1193 |
_version_ | 1783502493945167872 |
---|---|
author | Frandi, Antonio Collier, Justine |
author_facet | Frandi, Antonio Collier, Justine |
author_sort | Frandi, Antonio |
collection | PubMed |
description | Exquisite control of the DnaA initiator is critical to ensure that bacteria initiate chromosome replication in a cell cycle-coordinated manner. In many bacteria, the DnaA-related and replisome-associated Hda/HdaA protein interacts with DnaA to trigger the Regulatory Inactivation of DnaA (RIDA) and prevent over-initiation events. In the Caulobacter crescentus Alphaproteobacterium, the RIDA process also targets DnaA for its rapid proteolysis by Lon. The impact of the RIDA process on adaptation of bacteria to changing environments remains unexplored. Here, we identify a novel and conserved DnaA-related protein, named HdaB, and show that homologs from three different Alphaproteobacteria can inhibit the RIDA process, leading to over-initiation and cell death when expressed in actively growing C. crescentus cells. We further show that HdaB interacts with HdaA in vivo, most likely titrating HdaA away from DnaA. Strikingly, we find that HdaB accumulates mainly during stationary phase and that it shortens the lag phase upon exit from stationary phase. Altogether, these findings suggest that expression of hdaB during stationary phase prepares cells to restart the replication of their chromosome as soon as conditions improve, a situation often met by free-living or facultative intracellular Alphaproteobacteria. |
format | Online Article Text |
id | pubmed-7049699 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-70496992020-03-10 HdaB: a novel and conserved DnaA-related protein that targets the RIDA process to stimulate replication initiation Frandi, Antonio Collier, Justine Nucleic Acids Res Genome Integrity, Repair and Replication Exquisite control of the DnaA initiator is critical to ensure that bacteria initiate chromosome replication in a cell cycle-coordinated manner. In many bacteria, the DnaA-related and replisome-associated Hda/HdaA protein interacts with DnaA to trigger the Regulatory Inactivation of DnaA (RIDA) and prevent over-initiation events. In the Caulobacter crescentus Alphaproteobacterium, the RIDA process also targets DnaA for its rapid proteolysis by Lon. The impact of the RIDA process on adaptation of bacteria to changing environments remains unexplored. Here, we identify a novel and conserved DnaA-related protein, named HdaB, and show that homologs from three different Alphaproteobacteria can inhibit the RIDA process, leading to over-initiation and cell death when expressed in actively growing C. crescentus cells. We further show that HdaB interacts with HdaA in vivo, most likely titrating HdaA away from DnaA. Strikingly, we find that HdaB accumulates mainly during stationary phase and that it shortens the lag phase upon exit from stationary phase. Altogether, these findings suggest that expression of hdaB during stationary phase prepares cells to restart the replication of their chromosome as soon as conditions improve, a situation often met by free-living or facultative intracellular Alphaproteobacteria. Oxford University Press 2020-03-18 2019-12-25 /pmc/articles/PMC7049699/ /pubmed/31875223 http://dx.doi.org/10.1093/nar/gkz1193 Text en © The Author(s) 2019. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Genome Integrity, Repair and Replication Frandi, Antonio Collier, Justine HdaB: a novel and conserved DnaA-related protein that targets the RIDA process to stimulate replication initiation |
title | HdaB: a novel and conserved DnaA-related protein that targets the RIDA process to stimulate replication initiation |
title_full | HdaB: a novel and conserved DnaA-related protein that targets the RIDA process to stimulate replication initiation |
title_fullStr | HdaB: a novel and conserved DnaA-related protein that targets the RIDA process to stimulate replication initiation |
title_full_unstemmed | HdaB: a novel and conserved DnaA-related protein that targets the RIDA process to stimulate replication initiation |
title_short | HdaB: a novel and conserved DnaA-related protein that targets the RIDA process to stimulate replication initiation |
title_sort | hdab: a novel and conserved dnaa-related protein that targets the rida process to stimulate replication initiation |
topic | Genome Integrity, Repair and Replication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7049699/ https://www.ncbi.nlm.nih.gov/pubmed/31875223 http://dx.doi.org/10.1093/nar/gkz1193 |
work_keys_str_mv | AT frandiantonio hdabanovelandconserveddnaarelatedproteinthattargetstheridaprocesstostimulatereplicationinitiation AT collierjustine hdabanovelandconserveddnaarelatedproteinthattargetstheridaprocesstostimulatereplicationinitiation |