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Expanding the view on the evolution of the nematode dauer signalling pathways: refinement through gene gain and pathway co-option
BACKGROUND: Signalling pathways underlie development, behaviour and pathology. To understand patterns in the evolution of signalling pathways, we undertook a comprehensive investigation of the pathways that control the switch between growth and developmentally quiescent dauer in 24 species of nemato...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4924289/ https://www.ncbi.nlm.nih.gov/pubmed/27350342 http://dx.doi.org/10.1186/s12864-016-2770-7 |
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author | Gilabert, Aude Curran, David M. Harvey, Simon C. Wasmuth, James D. |
author_facet | Gilabert, Aude Curran, David M. Harvey, Simon C. Wasmuth, James D. |
author_sort | Gilabert, Aude |
collection | PubMed |
description | BACKGROUND: Signalling pathways underlie development, behaviour and pathology. To understand patterns in the evolution of signalling pathways, we undertook a comprehensive investigation of the pathways that control the switch between growth and developmentally quiescent dauer in 24 species of nematodes spanning the phylum. RESULTS: Our analysis of 47 genes across these species indicates that the pathways and their interactions are not conserved throughout the Nematoda. For example, the TGF-β pathway was co-opted into dauer control relatively late in a lineage that led to the model species Caenorhabditis elegans. We show molecular adaptations described in C. elegans that are restricted to its genus or even just to the species. Similarly, our analyses both identify species where particular genes have been lost and situations where apparently incorrect orthologues have been identified. CONCLUSIONS: Our analysis also highlights the difficulties of working with genome sequences from non-model species as reliance on the published gene models would have significantly restricted our understanding of how signalling pathways evolve. Our approach therefore offers a robust standard operating procedure for genomic comparisons. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-016-2770-7) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4924289 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-49242892016-06-29 Expanding the view on the evolution of the nematode dauer signalling pathways: refinement through gene gain and pathway co-option Gilabert, Aude Curran, David M. Harvey, Simon C. Wasmuth, James D. BMC Genomics Research Article BACKGROUND: Signalling pathways underlie development, behaviour and pathology. To understand patterns in the evolution of signalling pathways, we undertook a comprehensive investigation of the pathways that control the switch between growth and developmentally quiescent dauer in 24 species of nematodes spanning the phylum. RESULTS: Our analysis of 47 genes across these species indicates that the pathways and their interactions are not conserved throughout the Nematoda. For example, the TGF-β pathway was co-opted into dauer control relatively late in a lineage that led to the model species Caenorhabditis elegans. We show molecular adaptations described in C. elegans that are restricted to its genus or even just to the species. Similarly, our analyses both identify species where particular genes have been lost and situations where apparently incorrect orthologues have been identified. CONCLUSIONS: Our analysis also highlights the difficulties of working with genome sequences from non-model species as reliance on the published gene models would have significantly restricted our understanding of how signalling pathways evolve. Our approach therefore offers a robust standard operating procedure for genomic comparisons. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-016-2770-7) contains supplementary material, which is available to authorized users. BioMed Central 2016-06-27 /pmc/articles/PMC4924289/ /pubmed/27350342 http://dx.doi.org/10.1186/s12864-016-2770-7 Text en © The Author(s). 2016 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 Gilabert, Aude Curran, David M. Harvey, Simon C. Wasmuth, James D. Expanding the view on the evolution of the nematode dauer signalling pathways: refinement through gene gain and pathway co-option |
title | Expanding the view on the evolution of the nematode dauer signalling pathways: refinement through gene gain and pathway co-option |
title_full | Expanding the view on the evolution of the nematode dauer signalling pathways: refinement through gene gain and pathway co-option |
title_fullStr | Expanding the view on the evolution of the nematode dauer signalling pathways: refinement through gene gain and pathway co-option |
title_full_unstemmed | Expanding the view on the evolution of the nematode dauer signalling pathways: refinement through gene gain and pathway co-option |
title_short | Expanding the view on the evolution of the nematode dauer signalling pathways: refinement through gene gain and pathway co-option |
title_sort | expanding the view on the evolution of the nematode dauer signalling pathways: refinement through gene gain and pathway co-option |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4924289/ https://www.ncbi.nlm.nih.gov/pubmed/27350342 http://dx.doi.org/10.1186/s12864-016-2770-7 |
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