Cargando…
Plasticity first: molecular signatures of a complex morphological trait in filamentous cyanobacteria
BACKGROUND: Filamentous cyanobacteria that differentiate multiple cell types are considered the peak of prokaryotic complexity and their evolution has been studied in the context of multicellularity origins. Species that form true-branching filaments exemplify the most complex cyanobacteria. However...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5580265/ https://www.ncbi.nlm.nih.gov/pubmed/28859625 http://dx.doi.org/10.1186/s12862-017-1053-5 |
_version_ | 1783260875939905536 |
---|---|
author | Koch, Robin Kupczok, Anne Stucken, Karina Ilhan, Judith Hammerschmidt, Katrin Dagan, Tal |
author_facet | Koch, Robin Kupczok, Anne Stucken, Karina Ilhan, Judith Hammerschmidt, Katrin Dagan, Tal |
author_sort | Koch, Robin |
collection | PubMed |
description | BACKGROUND: Filamentous cyanobacteria that differentiate multiple cell types are considered the peak of prokaryotic complexity and their evolution has been studied in the context of multicellularity origins. Species that form true-branching filaments exemplify the most complex cyanobacteria. However, the mechanisms underlying the true-branching morphology remain poorly understood despite of several investigations that focused on the identification of novel genes or pathways. An alternative route for the evolution of novel traits is based on existing phenotypic plasticity. According to that scenario – termed genetic assimilation – the fixation of a novel phenotype precedes the fixation of the genotype. RESULTS: Here we show that the evolution of transcriptional regulatory elements constitutes a major mechanism for the evolution of new traits. We found that supplementation with sucrose reconstitutes the ancestral branchless phenotype of two true-branching Fischerella species and compared the transcription start sites (TSSs) between the two phenotypic states. Our analysis uncovers several orthologous TSSs whose transcription level is correlated with the true-branching phenotype. These TSSs are found in genes that encode components of the septosome and elongasome (e.g., fraC and mreB). CONCLUSIONS: The concept of genetic assimilation supplies a tenable explanation for the evolution of novel traits but testing its feasibility is hindered by the inability to recreate and study the evolution of present-day traits. We present a novel approach to examine transcription data for the plasticity first route and provide evidence for its occurrence during the evolution of complex colony morphology in true-branching cyanobacteria. Our results reveal a route for evolution of the true-branching phenotype in cyanobacteria via modification of the transcription level of pre-existing genes. Our study supplies evidence for the ‘plasticity-first’ hypothesis and highlights the importance of transcriptional regulation in the evolution of novel traits. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12862-017-1053-5) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5580265 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-55802652017-09-07 Plasticity first: molecular signatures of a complex morphological trait in filamentous cyanobacteria Koch, Robin Kupczok, Anne Stucken, Karina Ilhan, Judith Hammerschmidt, Katrin Dagan, Tal BMC Evol Biol Research Article BACKGROUND: Filamentous cyanobacteria that differentiate multiple cell types are considered the peak of prokaryotic complexity and their evolution has been studied in the context of multicellularity origins. Species that form true-branching filaments exemplify the most complex cyanobacteria. However, the mechanisms underlying the true-branching morphology remain poorly understood despite of several investigations that focused on the identification of novel genes or pathways. An alternative route for the evolution of novel traits is based on existing phenotypic plasticity. According to that scenario – termed genetic assimilation – the fixation of a novel phenotype precedes the fixation of the genotype. RESULTS: Here we show that the evolution of transcriptional regulatory elements constitutes a major mechanism for the evolution of new traits. We found that supplementation with sucrose reconstitutes the ancestral branchless phenotype of two true-branching Fischerella species and compared the transcription start sites (TSSs) between the two phenotypic states. Our analysis uncovers several orthologous TSSs whose transcription level is correlated with the true-branching phenotype. These TSSs are found in genes that encode components of the septosome and elongasome (e.g., fraC and mreB). CONCLUSIONS: The concept of genetic assimilation supplies a tenable explanation for the evolution of novel traits but testing its feasibility is hindered by the inability to recreate and study the evolution of present-day traits. We present a novel approach to examine transcription data for the plasticity first route and provide evidence for its occurrence during the evolution of complex colony morphology in true-branching cyanobacteria. Our results reveal a route for evolution of the true-branching phenotype in cyanobacteria via modification of the transcription level of pre-existing genes. Our study supplies evidence for the ‘plasticity-first’ hypothesis and highlights the importance of transcriptional regulation in the evolution of novel traits. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12862-017-1053-5) contains supplementary material, which is available to authorized users. BioMed Central 2017-08-31 /pmc/articles/PMC5580265/ /pubmed/28859625 http://dx.doi.org/10.1186/s12862-017-1053-5 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Koch, Robin Kupczok, Anne Stucken, Karina Ilhan, Judith Hammerschmidt, Katrin Dagan, Tal Plasticity first: molecular signatures of a complex morphological trait in filamentous cyanobacteria |
title | Plasticity first: molecular signatures of a complex morphological trait in filamentous cyanobacteria |
title_full | Plasticity first: molecular signatures of a complex morphological trait in filamentous cyanobacteria |
title_fullStr | Plasticity first: molecular signatures of a complex morphological trait in filamentous cyanobacteria |
title_full_unstemmed | Plasticity first: molecular signatures of a complex morphological trait in filamentous cyanobacteria |
title_short | Plasticity first: molecular signatures of a complex morphological trait in filamentous cyanobacteria |
title_sort | plasticity first: molecular signatures of a complex morphological trait in filamentous cyanobacteria |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5580265/ https://www.ncbi.nlm.nih.gov/pubmed/28859625 http://dx.doi.org/10.1186/s12862-017-1053-5 |
work_keys_str_mv | AT kochrobin plasticityfirstmolecularsignaturesofacomplexmorphologicaltraitinfilamentouscyanobacteria AT kupczokanne plasticityfirstmolecularsignaturesofacomplexmorphologicaltraitinfilamentouscyanobacteria AT stuckenkarina plasticityfirstmolecularsignaturesofacomplexmorphologicaltraitinfilamentouscyanobacteria AT ilhanjudith plasticityfirstmolecularsignaturesofacomplexmorphologicaltraitinfilamentouscyanobacteria AT hammerschmidtkatrin plasticityfirstmolecularsignaturesofacomplexmorphologicaltraitinfilamentouscyanobacteria AT dagantal plasticityfirstmolecularsignaturesofacomplexmorphologicaltraitinfilamentouscyanobacteria |