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Early fate of exogenous promoters in E. coli
Gene gain by horizontal gene transfer is a major pathway of genome innovation in bacteria. The current view posits that acquired genes initially need to be silenced and that a bacterial chromatin protein, H-NS, plays a role in this silencing. However, we lack direct observation of the early fate of...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7049719/ https://www.ncbi.nlm.nih.gov/pubmed/31960057 http://dx.doi.org/10.1093/nar/gkz1196 |
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author | Yousuf, Malikmohamed Iuliani, Ilaria Veetil, Reshma T Seshasayee, Aswin Sai Narain Sclavi, Bianca Cosentino Lagomarsino, Marco |
author_facet | Yousuf, Malikmohamed Iuliani, Ilaria Veetil, Reshma T Seshasayee, Aswin Sai Narain Sclavi, Bianca Cosentino Lagomarsino, Marco |
author_sort | Yousuf, Malikmohamed |
collection | PubMed |
description | Gene gain by horizontal gene transfer is a major pathway of genome innovation in bacteria. The current view posits that acquired genes initially need to be silenced and that a bacterial chromatin protein, H-NS, plays a role in this silencing. However, we lack direct observation of the early fate of a horizontally transferred gene to prove this theory. We combine sequencing, flow cytometry and sorting, followed by microscopy to monitor gene expression and its variability after large-scale random insertions of a reporter gene in a population of Escherichia coli bacteria. We find that inserted promoters have a wide range of gene-expression variability related to their location. We find that high-expression clones carry insertions that are not correlated with H-NS binding. Conversely, binding of H-NS correlates with silencing. Finally, while most promoters show a common level of extrinsic noise, some insertions show higher noise levels. Analysis of these high-noise clones supports a scenario of switching due to transcriptional interference from divergent ribosomal promoters. Altogether, our findings point to evolutionary pathways where newly-acquired genes are not necessarily silenced, but may immediately explore a wide range of expression levels to probe the optimal ones. |
format | Online Article Text |
id | pubmed-7049719 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-70497192020-03-10 Early fate of exogenous promoters in E. coli Yousuf, Malikmohamed Iuliani, Ilaria Veetil, Reshma T Seshasayee, Aswin Sai Narain Sclavi, Bianca Cosentino Lagomarsino, Marco Nucleic Acids Res Gene regulation, Chromatin and Epigenetics Gene gain by horizontal gene transfer is a major pathway of genome innovation in bacteria. The current view posits that acquired genes initially need to be silenced and that a bacterial chromatin protein, H-NS, plays a role in this silencing. However, we lack direct observation of the early fate of a horizontally transferred gene to prove this theory. We combine sequencing, flow cytometry and sorting, followed by microscopy to monitor gene expression and its variability after large-scale random insertions of a reporter gene in a population of Escherichia coli bacteria. We find that inserted promoters have a wide range of gene-expression variability related to their location. We find that high-expression clones carry insertions that are not correlated with H-NS binding. Conversely, binding of H-NS correlates with silencing. Finally, while most promoters show a common level of extrinsic noise, some insertions show higher noise levels. Analysis of these high-noise clones supports a scenario of switching due to transcriptional interference from divergent ribosomal promoters. Altogether, our findings point to evolutionary pathways where newly-acquired genes are not necessarily silenced, but may immediately explore a wide range of expression levels to probe the optimal ones. Oxford University Press 2020-03-18 2020-01-21 /pmc/articles/PMC7049719/ /pubmed/31960057 http://dx.doi.org/10.1093/nar/gkz1196 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Gene regulation, Chromatin and Epigenetics Yousuf, Malikmohamed Iuliani, Ilaria Veetil, Reshma T Seshasayee, Aswin Sai Narain Sclavi, Bianca Cosentino Lagomarsino, Marco Early fate of exogenous promoters in E. coli |
title | Early fate of exogenous promoters in E. coli |
title_full | Early fate of exogenous promoters in E. coli |
title_fullStr | Early fate of exogenous promoters in E. coli |
title_full_unstemmed | Early fate of exogenous promoters in E. coli |
title_short | Early fate of exogenous promoters in E. coli |
title_sort | early fate of exogenous promoters in e. coli |
topic | Gene regulation, Chromatin and Epigenetics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7049719/ https://www.ncbi.nlm.nih.gov/pubmed/31960057 http://dx.doi.org/10.1093/nar/gkz1196 |
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