Cargando…
Duplication and expression of Sox genes in spiders
BACKGROUND: The Sox family of transcription factors is an important part of the genetic ‘toolbox’ of all metazoans examined to date and is known to play important developmental roles in vertebrates and insects. However, outside the commonly studied Drosophila model little is known about the repertoi...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6307133/ https://www.ncbi.nlm.nih.gov/pubmed/30587109 http://dx.doi.org/10.1186/s12862-018-1337-4 |
_version_ | 1783382936092934144 |
---|---|
author | Bonatto Paese, Christian L. Leite, Daniel J. Schönauer, Anna McGregor, Alistair P. Russell, Steven |
author_facet | Bonatto Paese, Christian L. Leite, Daniel J. Schönauer, Anna McGregor, Alistair P. Russell, Steven |
author_sort | Bonatto Paese, Christian L. |
collection | PubMed |
description | BACKGROUND: The Sox family of transcription factors is an important part of the genetic ‘toolbox’ of all metazoans examined to date and is known to play important developmental roles in vertebrates and insects. However, outside the commonly studied Drosophila model little is known about the repertoire of Sox family transcription factors in other arthropod species. Here we characterise the Sox family in two chelicerate species, the spiders Parasteatoda tepidariorum and Stegodyphus mimosarum, which have experienced a whole genome duplication (WGD) in their evolutionary history. RESULTS: We find that virtually all of the duplicate Sox genes have been retained in these spiders after the WGD. Analysis of the expression of Sox genes in P. tepidariorum embryos suggests that it is likely that some of these genes have neofunctionalised after duplication. Our expression analysis also strengthens the view that an orthologue of vertebrate Group B1 genes, SoxNeuro, is implicated in the earliest events of CNS specification in both vertebrates and invertebrates. In addition, a gene in the Dichaete/Sox21b class is dynamically expressed in the spider segment addition zone, suggestive of an ancient regulatory mechanism controlling arthropod segmentation as recently suggested for flies and beetles. Together with the recent analysis of Sox gene expression in the embryos of other arthropods, our findings support the idea of conserved functions for some of these genes, including a potential role for SoxC and SoxD genes in CNS development and SoxF in limb development. CONCLUSIONS: Our study provides a new chelicerate perspective to understanding the evolution and function of Sox genes and how the retention of duplicates of such important tool-box genes after WGD has contributed to different aspects of spider embryogenesis. Future characterisation of the function of these genes in spiders will help us to better understand the evolution of the regulation of important developmental processes in arthropods and other metazoans including neurogenesis and segmentation. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12862-018-1337-4) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6307133 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-63071332019-01-02 Duplication and expression of Sox genes in spiders Bonatto Paese, Christian L. Leite, Daniel J. Schönauer, Anna McGregor, Alistair P. Russell, Steven BMC Evol Biol Research Article BACKGROUND: The Sox family of transcription factors is an important part of the genetic ‘toolbox’ of all metazoans examined to date and is known to play important developmental roles in vertebrates and insects. However, outside the commonly studied Drosophila model little is known about the repertoire of Sox family transcription factors in other arthropod species. Here we characterise the Sox family in two chelicerate species, the spiders Parasteatoda tepidariorum and Stegodyphus mimosarum, which have experienced a whole genome duplication (WGD) in their evolutionary history. RESULTS: We find that virtually all of the duplicate Sox genes have been retained in these spiders after the WGD. Analysis of the expression of Sox genes in P. tepidariorum embryos suggests that it is likely that some of these genes have neofunctionalised after duplication. Our expression analysis also strengthens the view that an orthologue of vertebrate Group B1 genes, SoxNeuro, is implicated in the earliest events of CNS specification in both vertebrates and invertebrates. In addition, a gene in the Dichaete/Sox21b class is dynamically expressed in the spider segment addition zone, suggestive of an ancient regulatory mechanism controlling arthropod segmentation as recently suggested for flies and beetles. Together with the recent analysis of Sox gene expression in the embryos of other arthropods, our findings support the idea of conserved functions for some of these genes, including a potential role for SoxC and SoxD genes in CNS development and SoxF in limb development. CONCLUSIONS: Our study provides a new chelicerate perspective to understanding the evolution and function of Sox genes and how the retention of duplicates of such important tool-box genes after WGD has contributed to different aspects of spider embryogenesis. Future characterisation of the function of these genes in spiders will help us to better understand the evolution of the regulation of important developmental processes in arthropods and other metazoans including neurogenesis and segmentation. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12862-018-1337-4) contains supplementary material, which is available to authorized users. BioMed Central 2018-12-27 /pmc/articles/PMC6307133/ /pubmed/30587109 http://dx.doi.org/10.1186/s12862-018-1337-4 Text en © The Author(s). 2018 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 Bonatto Paese, Christian L. Leite, Daniel J. Schönauer, Anna McGregor, Alistair P. Russell, Steven Duplication and expression of Sox genes in spiders |
title | Duplication and expression of Sox genes in spiders |
title_full | Duplication and expression of Sox genes in spiders |
title_fullStr | Duplication and expression of Sox genes in spiders |
title_full_unstemmed | Duplication and expression of Sox genes in spiders |
title_short | Duplication and expression of Sox genes in spiders |
title_sort | duplication and expression of sox genes in spiders |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6307133/ https://www.ncbi.nlm.nih.gov/pubmed/30587109 http://dx.doi.org/10.1186/s12862-018-1337-4 |
work_keys_str_mv | AT bonattopaesechristianl duplicationandexpressionofsoxgenesinspiders AT leitedanielj duplicationandexpressionofsoxgenesinspiders AT schonaueranna duplicationandexpressionofsoxgenesinspiders AT mcgregoralistairp duplicationandexpressionofsoxgenesinspiders AT russellsteven duplicationandexpressionofsoxgenesinspiders |