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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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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. |
format | Online Article Text |
id | pubmed-7732839 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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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