Cargando…
Repeated Phenotypic Evolution by Different Genetic Routes in Pseudomonas fluorescens SBW25
Repeated evolution of functionally similar phenotypes is observed throughout the tree of life. The extent to which the underlying genetics are conserved remains an area of considerable interest. Previously, we reported the evolution of colony switching in two independent lineages of Pseudomonas fluo...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6519391/ https://www.ncbi.nlm.nih.gov/pubmed/30835268 http://dx.doi.org/10.1093/molbev/msz040 |
_version_ | 1783418632791916544 |
---|---|
author | Gallie, Jenna Bertels, Frederic Remigi, Philippe Ferguson, Gayle C Nestmann, Sylke Rainey, Paul B |
author_facet | Gallie, Jenna Bertels, Frederic Remigi, Philippe Ferguson, Gayle C Nestmann, Sylke Rainey, Paul B |
author_sort | Gallie, Jenna |
collection | PubMed |
description | Repeated evolution of functionally similar phenotypes is observed throughout the tree of life. The extent to which the underlying genetics are conserved remains an area of considerable interest. Previously, we reported the evolution of colony switching in two independent lineages of Pseudomonas fluorescens SBW25. The phenotypic and genotypic bases of colony switching in the first lineage (Line 1) have been described elsewhere. Here, we deconstruct the evolution of colony switching in the second lineage (Line 6). We show that, as for Line 1, Line 6 colony switching results from an increase in the expression of a colanic acid-like polymer (CAP). At the genetic level, nine mutations occur in Line 6. Only one of these—a nonsynonymous point mutation in the housekeeping sigma factor rpoD—is required for colony switching. In contrast, the genetic basis of colony switching in Line 1 is a mutation in the metabolic gene carB. A molecular model has recently been proposed whereby the carB mutation increases capsulation by redressing the intracellular balance of positive (ribosomes) and negative (RsmAE/CsrA) regulators of a positive feedback loop in capsule expression. We show that Line 6 colony switching is consistent with this model; the rpoD mutation generates an increase in ribosomal gene expression, and ultimately an increase in CAP expression. |
format | Online Article Text |
id | pubmed-6519391 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-65193912019-05-20 Repeated Phenotypic Evolution by Different Genetic Routes in Pseudomonas fluorescens SBW25 Gallie, Jenna Bertels, Frederic Remigi, Philippe Ferguson, Gayle C Nestmann, Sylke Rainey, Paul B Mol Biol Evol Discoveries Repeated evolution of functionally similar phenotypes is observed throughout the tree of life. The extent to which the underlying genetics are conserved remains an area of considerable interest. Previously, we reported the evolution of colony switching in two independent lineages of Pseudomonas fluorescens SBW25. The phenotypic and genotypic bases of colony switching in the first lineage (Line 1) have been described elsewhere. Here, we deconstruct the evolution of colony switching in the second lineage (Line 6). We show that, as for Line 1, Line 6 colony switching results from an increase in the expression of a colanic acid-like polymer (CAP). At the genetic level, nine mutations occur in Line 6. Only one of these—a nonsynonymous point mutation in the housekeeping sigma factor rpoD—is required for colony switching. In contrast, the genetic basis of colony switching in Line 1 is a mutation in the metabolic gene carB. A molecular model has recently been proposed whereby the carB mutation increases capsulation by redressing the intracellular balance of positive (ribosomes) and negative (RsmAE/CsrA) regulators of a positive feedback loop in capsule expression. We show that Line 6 colony switching is consistent with this model; the rpoD mutation generates an increase in ribosomal gene expression, and ultimately an increase in CAP expression. Oxford University Press 2019-05 2019-03-05 /pmc/articles/PMC6519391/ /pubmed/30835268 http://dx.doi.org/10.1093/molbev/msz040 Text en © The Author(s) 2019. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. 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 | Discoveries Gallie, Jenna Bertels, Frederic Remigi, Philippe Ferguson, Gayle C Nestmann, Sylke Rainey, Paul B Repeated Phenotypic Evolution by Different Genetic Routes in Pseudomonas fluorescens SBW25 |
title | Repeated Phenotypic Evolution by Different Genetic Routes in Pseudomonas fluorescens SBW25 |
title_full | Repeated Phenotypic Evolution by Different Genetic Routes in Pseudomonas fluorescens SBW25 |
title_fullStr | Repeated Phenotypic Evolution by Different Genetic Routes in Pseudomonas fluorescens SBW25 |
title_full_unstemmed | Repeated Phenotypic Evolution by Different Genetic Routes in Pseudomonas fluorescens SBW25 |
title_short | Repeated Phenotypic Evolution by Different Genetic Routes in Pseudomonas fluorescens SBW25 |
title_sort | repeated phenotypic evolution by different genetic routes in pseudomonas fluorescens sbw25 |
topic | Discoveries |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6519391/ https://www.ncbi.nlm.nih.gov/pubmed/30835268 http://dx.doi.org/10.1093/molbev/msz040 |
work_keys_str_mv | AT galliejenna repeatedphenotypicevolutionbydifferentgeneticroutesinpseudomonasfluorescenssbw25 AT bertelsfrederic repeatedphenotypicevolutionbydifferentgeneticroutesinpseudomonasfluorescenssbw25 AT remigiphilippe repeatedphenotypicevolutionbydifferentgeneticroutesinpseudomonasfluorescenssbw25 AT fergusongaylec repeatedphenotypicevolutionbydifferentgeneticroutesinpseudomonasfluorescenssbw25 AT nestmannsylke repeatedphenotypicevolutionbydifferentgeneticroutesinpseudomonasfluorescenssbw25 AT raineypaulb repeatedphenotypicevolutionbydifferentgeneticroutesinpseudomonasfluorescenssbw25 |