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Machine learning uncovers independently regulated modules in the Bacillus subtilis transcriptome

The transcriptional regulatory network (TRN) of Bacillus subtilis coordinates cellular functions of fundamental interest, including metabolism, biofilm formation, and sporulation. Here, we use unsupervised machine learning to modularize the transcriptome and quantitatively describe regulatory activi...

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Detalles Bibliográficos
Autores principales: Rychel, Kevin, Sastry, Anand V., Palsson, Bernhard O.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7732839/
https://www.ncbi.nlm.nih.gov/pubmed/33311500
http://dx.doi.org/10.1038/s41467-020-20153-9
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author Rychel, Kevin
Sastry, Anand V.
Palsson, Bernhard O.
author_facet Rychel, Kevin
Sastry, Anand V.
Palsson, Bernhard O.
author_sort Rychel, Kevin
collection PubMed
description The transcriptional regulatory network (TRN) of Bacillus subtilis coordinates cellular functions of fundamental interest, including metabolism, biofilm formation, and sporulation. Here, we use unsupervised machine learning to modularize the transcriptome and quantitatively describe regulatory activity under diverse conditions, creating an unbiased summary of gene expression. We obtain 83 independently modulated gene sets that explain most of the variance in expression and demonstrate that 76% of them represent the effects of known regulators. The TRN structure and its condition-dependent activity uncover putative or recently discovered roles for at least five regulons, such as a relationship between histidine utilization and quorum sensing. The TRN also facilitates quantification of population-level sporulation states. As this TRN covers the majority of the transcriptome and concisely characterizes the global expression state, it could inform research on nearly every aspect of transcriptional regulation in B. subtilis.
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spelling pubmed-77328392020-12-17 Machine learning uncovers independently regulated modules in the Bacillus subtilis transcriptome Rychel, Kevin Sastry, Anand V. Palsson, Bernhard O. Nat Commun Article The transcriptional regulatory network (TRN) of Bacillus subtilis coordinates cellular functions of fundamental interest, including metabolism, biofilm formation, and sporulation. Here, we use unsupervised machine learning to modularize the transcriptome and quantitatively describe regulatory activity under diverse conditions, creating an unbiased summary of gene expression. We obtain 83 independently modulated gene sets that explain most of the variance in expression and demonstrate that 76% of them represent the effects of known regulators. The TRN structure and its condition-dependent activity uncover putative or recently discovered roles for at least five regulons, such as a relationship between histidine utilization and quorum sensing. The TRN also facilitates quantification of population-level sporulation states. As this TRN covers the majority of the transcriptome and concisely characterizes the global expression state, it could inform research on nearly every aspect of transcriptional regulation in B. subtilis. Nature Publishing Group UK 2020-12-11 /pmc/articles/PMC7732839/ /pubmed/33311500 http://dx.doi.org/10.1038/s41467-020-20153-9 Text en © The Author(s) 2020 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/.
spellingShingle Article
Rychel, Kevin
Sastry, Anand V.
Palsson, Bernhard O.
Machine learning uncovers independently regulated modules in the Bacillus subtilis transcriptome
title Machine learning uncovers independently regulated modules in the Bacillus subtilis transcriptome
title_full Machine learning uncovers independently regulated modules in the Bacillus subtilis transcriptome
title_fullStr Machine learning uncovers independently regulated modules in the Bacillus subtilis transcriptome
title_full_unstemmed Machine learning uncovers independently regulated modules in the Bacillus subtilis transcriptome
title_short Machine learning uncovers independently regulated modules in the Bacillus subtilis transcriptome
title_sort machine learning uncovers independently regulated modules in the bacillus subtilis transcriptome
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7732839/
https://www.ncbi.nlm.nih.gov/pubmed/33311500
http://dx.doi.org/10.1038/s41467-020-20153-9
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