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Manipulating the Bacterial Cell Cycle and Cell Size by Titrating the Expression of Ribonucleotide Reductase
Understanding how bacteria coordinate growth with cell cycle events to maintain cell size homeostasis remains a grand challenge in biology. The period of chromosome replication (C period) is a key stage in the bacterial cell cycle. However, the mechanism of in vivo regulation of the C period remains...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Microbiology
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5686538/ https://www.ncbi.nlm.nih.gov/pubmed/29138305 http://dx.doi.org/10.1128/mBio.01741-17 |
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author | Zhu, Manlu Dai, Xiongfeng Guo, Weilun Ge, Zengxiang Yang, Mingxuan Wang, Haikuan Wang, Yi-Ping |
author_facet | Zhu, Manlu Dai, Xiongfeng Guo, Weilun Ge, Zengxiang Yang, Mingxuan Wang, Haikuan Wang, Yi-Ping |
author_sort | Zhu, Manlu |
collection | PubMed |
description | Understanding how bacteria coordinate growth with cell cycle events to maintain cell size homeostasis remains a grand challenge in biology. The period of chromosome replication (C period) is a key stage in the bacterial cell cycle. However, the mechanism of in vivo regulation of the C period remains unclear. In this study, we found that titration of the expression of ribonucleotide reductase (RNR), which changes the intracellular deoxynucleoside triphosphate (dNTP) pools, enables significant perturbations of the C period, leading to a substantial change in cell size and DNA content. Our work demonstrates that the intracellular dNTP pool is indeed an important parameter that controls the progression of chromosome replication. Specially, RNR overexpression leads to a shortened C period compared with that of a wild-type strain growing under different nutrient conditions, indicating that the dNTP substrate levels are subsaturated under physiological conditions. In addition, perturbing the C period does not significantly change the D period, indicating that these two processes are largely independent from each other. Overall, titration of ribonucleotide reductase expression can serve as a standard model system for studying the coordination between chromosome replication, cell division, and cell size. |
format | Online Article Text |
id | pubmed-5686538 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | American Society for Microbiology |
record_format | MEDLINE/PubMed |
spelling | pubmed-56865382017-11-17 Manipulating the Bacterial Cell Cycle and Cell Size by Titrating the Expression of Ribonucleotide Reductase Zhu, Manlu Dai, Xiongfeng Guo, Weilun Ge, Zengxiang Yang, Mingxuan Wang, Haikuan Wang, Yi-Ping mBio Observation Understanding how bacteria coordinate growth with cell cycle events to maintain cell size homeostasis remains a grand challenge in biology. The period of chromosome replication (C period) is a key stage in the bacterial cell cycle. However, the mechanism of in vivo regulation of the C period remains unclear. In this study, we found that titration of the expression of ribonucleotide reductase (RNR), which changes the intracellular deoxynucleoside triphosphate (dNTP) pools, enables significant perturbations of the C period, leading to a substantial change in cell size and DNA content. Our work demonstrates that the intracellular dNTP pool is indeed an important parameter that controls the progression of chromosome replication. Specially, RNR overexpression leads to a shortened C period compared with that of a wild-type strain growing under different nutrient conditions, indicating that the dNTP substrate levels are subsaturated under physiological conditions. In addition, perturbing the C period does not significantly change the D period, indicating that these two processes are largely independent from each other. Overall, titration of ribonucleotide reductase expression can serve as a standard model system for studying the coordination between chromosome replication, cell division, and cell size. American Society for Microbiology 2017-11-14 /pmc/articles/PMC5686538/ /pubmed/29138305 http://dx.doi.org/10.1128/mBio.01741-17 Text en Copyright © 2017 Zhu et al. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Observation Zhu, Manlu Dai, Xiongfeng Guo, Weilun Ge, Zengxiang Yang, Mingxuan Wang, Haikuan Wang, Yi-Ping Manipulating the Bacterial Cell Cycle and Cell Size by Titrating the Expression of Ribonucleotide Reductase |
title | Manipulating the Bacterial Cell Cycle and Cell Size by Titrating the Expression of Ribonucleotide Reductase |
title_full | Manipulating the Bacterial Cell Cycle and Cell Size by Titrating the Expression of Ribonucleotide Reductase |
title_fullStr | Manipulating the Bacterial Cell Cycle and Cell Size by Titrating the Expression of Ribonucleotide Reductase |
title_full_unstemmed | Manipulating the Bacterial Cell Cycle and Cell Size by Titrating the Expression of Ribonucleotide Reductase |
title_short | Manipulating the Bacterial Cell Cycle and Cell Size by Titrating the Expression of Ribonucleotide Reductase |
title_sort | manipulating the bacterial cell cycle and cell size by titrating the expression of ribonucleotide reductase |
topic | Observation |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5686538/ https://www.ncbi.nlm.nih.gov/pubmed/29138305 http://dx.doi.org/10.1128/mBio.01741-17 |
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