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Stochastic transcriptional pulses orchestrate flagellar biosynthesis in Escherichia coli

The classic picture of flagellum biosynthesis in Escherichia coli, inferred from population measurements, depicts a deterministic program where promoters are sequentially up-regulated and are maintained steadily active throughout exponential growth. However, complex regulatory dynamics at the single...

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Autores principales: Kim, J. Mark, Garcia-Alcala, Mayra, Balleza, Enrique, Cluzel, Philippe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7002133/
https://www.ncbi.nlm.nih.gov/pubmed/32076637
http://dx.doi.org/10.1126/sciadv.aax0947
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author Kim, J. Mark
Garcia-Alcala, Mayra
Balleza, Enrique
Cluzel, Philippe
author_facet Kim, J. Mark
Garcia-Alcala, Mayra
Balleza, Enrique
Cluzel, Philippe
author_sort Kim, J. Mark
collection PubMed
description The classic picture of flagellum biosynthesis in Escherichia coli, inferred from population measurements, depicts a deterministic program where promoters are sequentially up-regulated and are maintained steadily active throughout exponential growth. However, complex regulatory dynamics at the single-cell level can be masked by bulk measurements. Here, we discover that in individual E. coli cells, flagellar promoters are stochastically activated in pulses. These pulses are coordinated within specific classes of promoters and comprise “on” and “off” states, each of which can span multiple generations. We demonstrate that in this pulsing program, the regulatory logic of flagellar assembly dictates which promoters skip pulses. Surprisingly, pulses do not require specific transcriptional or translational regulation of the flagellar master regulator, FlhDC, but instead appears to be essentially governed by an autonomous posttranslational circuit. Our results suggest that even topologically simple transcriptional networks can generate unexpectedly rich temporal dynamics and phenotypic heterogeneities.
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spelling pubmed-70021332020-02-19 Stochastic transcriptional pulses orchestrate flagellar biosynthesis in Escherichia coli Kim, J. Mark Garcia-Alcala, Mayra Balleza, Enrique Cluzel, Philippe Sci Adv Research Articles The classic picture of flagellum biosynthesis in Escherichia coli, inferred from population measurements, depicts a deterministic program where promoters are sequentially up-regulated and are maintained steadily active throughout exponential growth. However, complex regulatory dynamics at the single-cell level can be masked by bulk measurements. Here, we discover that in individual E. coli cells, flagellar promoters are stochastically activated in pulses. These pulses are coordinated within specific classes of promoters and comprise “on” and “off” states, each of which can span multiple generations. We demonstrate that in this pulsing program, the regulatory logic of flagellar assembly dictates which promoters skip pulses. Surprisingly, pulses do not require specific transcriptional or translational regulation of the flagellar master regulator, FlhDC, but instead appears to be essentially governed by an autonomous posttranslational circuit. Our results suggest that even topologically simple transcriptional networks can generate unexpectedly rich temporal dynamics and phenotypic heterogeneities. American Association for the Advancement of Science 2020-02-05 /pmc/articles/PMC7002133/ /pubmed/32076637 http://dx.doi.org/10.1126/sciadv.aax0947 Text en Copyright © 2020 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). http://creativecommons.org/licenses/by-nc/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (http://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited.
spellingShingle Research Articles
Kim, J. Mark
Garcia-Alcala, Mayra
Balleza, Enrique
Cluzel, Philippe
Stochastic transcriptional pulses orchestrate flagellar biosynthesis in Escherichia coli
title Stochastic transcriptional pulses orchestrate flagellar biosynthesis in Escherichia coli
title_full Stochastic transcriptional pulses orchestrate flagellar biosynthesis in Escherichia coli
title_fullStr Stochastic transcriptional pulses orchestrate flagellar biosynthesis in Escherichia coli
title_full_unstemmed Stochastic transcriptional pulses orchestrate flagellar biosynthesis in Escherichia coli
title_short Stochastic transcriptional pulses orchestrate flagellar biosynthesis in Escherichia coli
title_sort stochastic transcriptional pulses orchestrate flagellar biosynthesis in escherichia coli
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7002133/
https://www.ncbi.nlm.nih.gov/pubmed/32076637
http://dx.doi.org/10.1126/sciadv.aax0947
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