Cargando…

Large-scale gene expression study in the ophiuroid Amphiura filiformis provides insights into evolution of gene regulatory networks

BACKGROUND: The evolutionary mechanisms involved in shaping complex gene regulatory networks (GRN) that encode for morphologically similar structures in distantly related animals remain elusive. In this context, echinoderm larval skeletons found in brittle stars and sea urchins provide an ideal syst...

Descripción completa

Detalles Bibliográficos
Autores principales: Dylus, David Viktor, Czarkwiani, Anna, Stångberg, Josefine, Ortega-Martinez, Olga, Dupont, Sam, Oliveri, Paola
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4709884/
https://www.ncbi.nlm.nih.gov/pubmed/26759711
http://dx.doi.org/10.1186/s13227-015-0039-x
_version_ 1782409731525050368
author Dylus, David Viktor
Czarkwiani, Anna
Stångberg, Josefine
Ortega-Martinez, Olga
Dupont, Sam
Oliveri, Paola
author_facet Dylus, David Viktor
Czarkwiani, Anna
Stångberg, Josefine
Ortega-Martinez, Olga
Dupont, Sam
Oliveri, Paola
author_sort Dylus, David Viktor
collection PubMed
description BACKGROUND: The evolutionary mechanisms involved in shaping complex gene regulatory networks (GRN) that encode for morphologically similar structures in distantly related animals remain elusive. In this context, echinoderm larval skeletons found in brittle stars and sea urchins provide an ideal system. Here, we characterize for the first time the development of the larval skeleton in the ophiuroid Amphiura filiformis and compare it systematically with its counterpart in sea urchin. RESULTS: We show that ophiuroids and euechinoids, that split at least 480 Million years ago (Mya), have remarkable similarities in tempo and mode of skeletal development. Despite morphological and ontological similarities, our high-resolution study of the dynamics of genetic regulatory states in A. filiformis highlights numerous differences in the architecture of their underlying GRNs. Importantly, the A.filiformispplx, the closest gene to the sea urchin double negative gate (DNG) repressor pmar1, fails to drive the skeletogenic program in sea urchin, showing important evolutionary differences in protein function. hesC, the second repressor of the DNG, is co-expressed with most of the genes that are repressed in sea urchin, indicating the absence of direct repression of tbr, ets1/2, and delta in A. filiformis. Furthermore, the absence of expression in later stages of brittle star skeleton development of key regulatory genes, such as foxb and dri, shows significantly different regulatory states. CONCLUSION: Our data fill up an important gap in the picture of larval mesoderm in echinoderms and allows us to explore the evolutionary implications relative to the recently established phylogeny of echinoderm classes. In light of recent studies on other echinoderms, our data highlight a high evolutionary plasticity of the same nodes throughout evolution of echinoderm skeletogenesis. Finally, gene duplication, protein function diversification, and cis-regulatory element evolution all contributed to shape the regulatory program for larval skeletogenesis in different branches of echinoderms. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13227-015-0039-x) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-4709884
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-47098842016-01-13 Large-scale gene expression study in the ophiuroid Amphiura filiformis provides insights into evolution of gene regulatory networks Dylus, David Viktor Czarkwiani, Anna Stångberg, Josefine Ortega-Martinez, Olga Dupont, Sam Oliveri, Paola EvoDevo Research BACKGROUND: The evolutionary mechanisms involved in shaping complex gene regulatory networks (GRN) that encode for morphologically similar structures in distantly related animals remain elusive. In this context, echinoderm larval skeletons found in brittle stars and sea urchins provide an ideal system. Here, we characterize for the first time the development of the larval skeleton in the ophiuroid Amphiura filiformis and compare it systematically with its counterpart in sea urchin. RESULTS: We show that ophiuroids and euechinoids, that split at least 480 Million years ago (Mya), have remarkable similarities in tempo and mode of skeletal development. Despite morphological and ontological similarities, our high-resolution study of the dynamics of genetic regulatory states in A. filiformis highlights numerous differences in the architecture of their underlying GRNs. Importantly, the A.filiformispplx, the closest gene to the sea urchin double negative gate (DNG) repressor pmar1, fails to drive the skeletogenic program in sea urchin, showing important evolutionary differences in protein function. hesC, the second repressor of the DNG, is co-expressed with most of the genes that are repressed in sea urchin, indicating the absence of direct repression of tbr, ets1/2, and delta in A. filiformis. Furthermore, the absence of expression in later stages of brittle star skeleton development of key regulatory genes, such as foxb and dri, shows significantly different regulatory states. CONCLUSION: Our data fill up an important gap in the picture of larval mesoderm in echinoderms and allows us to explore the evolutionary implications relative to the recently established phylogeny of echinoderm classes. In light of recent studies on other echinoderms, our data highlight a high evolutionary plasticity of the same nodes throughout evolution of echinoderm skeletogenesis. Finally, gene duplication, protein function diversification, and cis-regulatory element evolution all contributed to shape the regulatory program for larval skeletogenesis in different branches of echinoderms. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13227-015-0039-x) contains supplementary material, which is available to authorized users. BioMed Central 2016-01-11 /pmc/articles/PMC4709884/ /pubmed/26759711 http://dx.doi.org/10.1186/s13227-015-0039-x Text en © Dylus et al. 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
Dylus, David Viktor
Czarkwiani, Anna
Stångberg, Josefine
Ortega-Martinez, Olga
Dupont, Sam
Oliveri, Paola
Large-scale gene expression study in the ophiuroid Amphiura filiformis provides insights into evolution of gene regulatory networks
title Large-scale gene expression study in the ophiuroid Amphiura filiformis provides insights into evolution of gene regulatory networks
title_full Large-scale gene expression study in the ophiuroid Amphiura filiformis provides insights into evolution of gene regulatory networks
title_fullStr Large-scale gene expression study in the ophiuroid Amphiura filiformis provides insights into evolution of gene regulatory networks
title_full_unstemmed Large-scale gene expression study in the ophiuroid Amphiura filiformis provides insights into evolution of gene regulatory networks
title_short Large-scale gene expression study in the ophiuroid Amphiura filiformis provides insights into evolution of gene regulatory networks
title_sort large-scale gene expression study in the ophiuroid amphiura filiformis provides insights into evolution of gene regulatory networks
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4709884/
https://www.ncbi.nlm.nih.gov/pubmed/26759711
http://dx.doi.org/10.1186/s13227-015-0039-x
work_keys_str_mv AT dylusdavidviktor largescalegeneexpressionstudyintheophiuroidamphiurafiliformisprovidesinsightsintoevolutionofgeneregulatorynetworks
AT czarkwianianna largescalegeneexpressionstudyintheophiuroidamphiurafiliformisprovidesinsightsintoevolutionofgeneregulatorynetworks
AT stangbergjosefine largescalegeneexpressionstudyintheophiuroidamphiurafiliformisprovidesinsightsintoevolutionofgeneregulatorynetworks
AT ortegamartinezolga largescalegeneexpressionstudyintheophiuroidamphiurafiliformisprovidesinsightsintoevolutionofgeneregulatorynetworks
AT dupontsam largescalegeneexpressionstudyintheophiuroidamphiurafiliformisprovidesinsightsintoevolutionofgeneregulatorynetworks
AT oliveripaola largescalegeneexpressionstudyintheophiuroidamphiurafiliformisprovidesinsightsintoevolutionofgeneregulatorynetworks