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Damage dynamics and the role of chance in the timing of E. coli cell death
Genetically identical cells in the same stressful condition die at different times. The origin of this stochasticity is unclear; it may arise from different initial conditions that affect the time of demise, or from a stochastic damage accumulation mechanism that erases the initial conditions and in...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10113371/ https://www.ncbi.nlm.nih.gov/pubmed/37072447 http://dx.doi.org/10.1038/s41467-023-37930-x |
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author | Yang, Yifan Karin, Omer Mayo, Avi Song, Xiaohu Chen, Peipei Santos, Ana L. Lindner, Ariel B. Alon, Uri |
author_facet | Yang, Yifan Karin, Omer Mayo, Avi Song, Xiaohu Chen, Peipei Santos, Ana L. Lindner, Ariel B. Alon, Uri |
author_sort | Yang, Yifan |
collection | PubMed |
description | Genetically identical cells in the same stressful condition die at different times. The origin of this stochasticity is unclear; it may arise from different initial conditions that affect the time of demise, or from a stochastic damage accumulation mechanism that erases the initial conditions and instead amplifies noise to generate different lifespans. To address this requires measuring damage dynamics in individual cells over the lifespan, but this has rarely been achieved. Here, we used a microfluidic device to measure membrane damage in 635 carbon-starved Escherichia coli cells at high temporal resolution. We find that initial conditions of damage, size or cell-cycle phase do not explain most of the lifespan variation. Instead, the data points to a stochastic mechanism in which noise is amplified by a rising production of damage that saturates its own removal. Surprisingly, the relative variation in damage drops with age: cells become more similar to each other in terms of relative damage, indicating increasing determinism with age. Thus, chance erases initial conditions and then gives way to increasingly deterministic dynamics that dominate the lifespan distribution. |
format | Online Article Text |
id | pubmed-10113371 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-101133712023-04-20 Damage dynamics and the role of chance in the timing of E. coli cell death Yang, Yifan Karin, Omer Mayo, Avi Song, Xiaohu Chen, Peipei Santos, Ana L. Lindner, Ariel B. Alon, Uri Nat Commun Article Genetically identical cells in the same stressful condition die at different times. The origin of this stochasticity is unclear; it may arise from different initial conditions that affect the time of demise, or from a stochastic damage accumulation mechanism that erases the initial conditions and instead amplifies noise to generate different lifespans. To address this requires measuring damage dynamics in individual cells over the lifespan, but this has rarely been achieved. Here, we used a microfluidic device to measure membrane damage in 635 carbon-starved Escherichia coli cells at high temporal resolution. We find that initial conditions of damage, size or cell-cycle phase do not explain most of the lifespan variation. Instead, the data points to a stochastic mechanism in which noise is amplified by a rising production of damage that saturates its own removal. Surprisingly, the relative variation in damage drops with age: cells become more similar to each other in terms of relative damage, indicating increasing determinism with age. Thus, chance erases initial conditions and then gives way to increasingly deterministic dynamics that dominate the lifespan distribution. Nature Publishing Group UK 2023-04-18 /pmc/articles/PMC10113371/ /pubmed/37072447 http://dx.doi.org/10.1038/s41467-023-37930-x Text en © The Author(s) 2023, corrected publication 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Yang, Yifan Karin, Omer Mayo, Avi Song, Xiaohu Chen, Peipei Santos, Ana L. Lindner, Ariel B. Alon, Uri Damage dynamics and the role of chance in the timing of E. coli cell death |
title | Damage dynamics and the role of chance in the timing of E. coli cell death |
title_full | Damage dynamics and the role of chance in the timing of E. coli cell death |
title_fullStr | Damage dynamics and the role of chance in the timing of E. coli cell death |
title_full_unstemmed | Damage dynamics and the role of chance in the timing of E. coli cell death |
title_short | Damage dynamics and the role of chance in the timing of E. coli cell death |
title_sort | damage dynamics and the role of chance in the timing of e. coli cell death |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10113371/ https://www.ncbi.nlm.nih.gov/pubmed/37072447 http://dx.doi.org/10.1038/s41467-023-37930-x |
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