Cargando…

The evolution of ependymin-related proteins

BACKGROUND: Ependymins were originally defined as fish-specific secreted glycoproteins involved in central nervous system plasticity and memory formation. Subsequent research revealed that these proteins represent a fish-specific lineage of a larger ependymin-related protein family (EPDRs). EPDRs ha...

Descripción completa

Detalles Bibliográficos
Autores principales: McDougall, Carmel, Hammond, Michael J., Dailey, Simon C., Somorjai, Ildiko M. L., Cummins, Scott F., Degnan, Bernard M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6280359/
https://www.ncbi.nlm.nih.gov/pubmed/30514200
http://dx.doi.org/10.1186/s12862-018-1306-y
_version_ 1783378652364275712
author McDougall, Carmel
Hammond, Michael J.
Dailey, Simon C.
Somorjai, Ildiko M. L.
Cummins, Scott F.
Degnan, Bernard M.
author_facet McDougall, Carmel
Hammond, Michael J.
Dailey, Simon C.
Somorjai, Ildiko M. L.
Cummins, Scott F.
Degnan, Bernard M.
author_sort McDougall, Carmel
collection PubMed
description BACKGROUND: Ependymins were originally defined as fish-specific secreted glycoproteins involved in central nervous system plasticity and memory formation. Subsequent research revealed that these proteins represent a fish-specific lineage of a larger ependymin-related protein family (EPDRs). EPDRs have now been identified in a number of bilaterian animals and have been implicated in diverse non-neural functions. The recent discoveries of putative EPDRs in unicellular holozoans and an expanded EPDR family with potential roles in conspecific communication in crown-of-thorns starfish suggest that the distribution and diversity of EPDRs is significantly broader than currently understood. RESULTS: We undertook a systematic survey to determine the distribution and evolution of EPDRs in eukaryotes. In addition to Bilateria, EPDR genes were identified in Cnidaria, Placozoa, Porifera, Choanoflagellatea, Filasterea, Apusozoa, Amoebozoa, Charophyta and Percolozoa, and tentatively in Cercozoa and the orphan group Malawimonadidae. EPDRs appear to be absent from prokaryotes and many eukaryote groups including ecdysozoans, fungi, stramenopiles, alveolates, haptistans and cryptistans. The EPDR family can be divided into two major clades and has undergone lineage-specific expansions in a number of metazoan lineages, including in poriferans, molluscs and cephalochordates. Variation in a core set of conserved residues in EPDRs reveals the presence of three distinct protein types; however, 3D modelling predicts overall protein structures to be similar. CONCLUSIONS: Our results reveal an early eukaryotic origin of the EPDR gene family and a dynamic pattern of gene duplication and gene loss in animals. This research provides a phylogenetic framework for the analysis of the functional evolution of this gene family. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12862-018-1306-y) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-6280359
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-62803592018-12-10 The evolution of ependymin-related proteins McDougall, Carmel Hammond, Michael J. Dailey, Simon C. Somorjai, Ildiko M. L. Cummins, Scott F. Degnan, Bernard M. BMC Evol Biol Research Article BACKGROUND: Ependymins were originally defined as fish-specific secreted glycoproteins involved in central nervous system plasticity and memory formation. Subsequent research revealed that these proteins represent a fish-specific lineage of a larger ependymin-related protein family (EPDRs). EPDRs have now been identified in a number of bilaterian animals and have been implicated in diverse non-neural functions. The recent discoveries of putative EPDRs in unicellular holozoans and an expanded EPDR family with potential roles in conspecific communication in crown-of-thorns starfish suggest that the distribution and diversity of EPDRs is significantly broader than currently understood. RESULTS: We undertook a systematic survey to determine the distribution and evolution of EPDRs in eukaryotes. In addition to Bilateria, EPDR genes were identified in Cnidaria, Placozoa, Porifera, Choanoflagellatea, Filasterea, Apusozoa, Amoebozoa, Charophyta and Percolozoa, and tentatively in Cercozoa and the orphan group Malawimonadidae. EPDRs appear to be absent from prokaryotes and many eukaryote groups including ecdysozoans, fungi, stramenopiles, alveolates, haptistans and cryptistans. The EPDR family can be divided into two major clades and has undergone lineage-specific expansions in a number of metazoan lineages, including in poriferans, molluscs and cephalochordates. Variation in a core set of conserved residues in EPDRs reveals the presence of three distinct protein types; however, 3D modelling predicts overall protein structures to be similar. CONCLUSIONS: Our results reveal an early eukaryotic origin of the EPDR gene family and a dynamic pattern of gene duplication and gene loss in animals. This research provides a phylogenetic framework for the analysis of the functional evolution of this gene family. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12862-018-1306-y) contains supplementary material, which is available to authorized users. BioMed Central 2018-12-04 /pmc/articles/PMC6280359/ /pubmed/30514200 http://dx.doi.org/10.1186/s12862-018-1306-y 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
McDougall, Carmel
Hammond, Michael J.
Dailey, Simon C.
Somorjai, Ildiko M. L.
Cummins, Scott F.
Degnan, Bernard M.
The evolution of ependymin-related proteins
title The evolution of ependymin-related proteins
title_full The evolution of ependymin-related proteins
title_fullStr The evolution of ependymin-related proteins
title_full_unstemmed The evolution of ependymin-related proteins
title_short The evolution of ependymin-related proteins
title_sort evolution of ependymin-related proteins
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6280359/
https://www.ncbi.nlm.nih.gov/pubmed/30514200
http://dx.doi.org/10.1186/s12862-018-1306-y
work_keys_str_mv AT mcdougallcarmel theevolutionofependyminrelatedproteins
AT hammondmichaelj theevolutionofependyminrelatedproteins
AT daileysimonc theevolutionofependyminrelatedproteins
AT somorjaiildikoml theevolutionofependyminrelatedproteins
AT cumminsscottf theevolutionofependyminrelatedproteins
AT degnanbernardm theevolutionofependyminrelatedproteins
AT mcdougallcarmel evolutionofependyminrelatedproteins
AT hammondmichaelj evolutionofependyminrelatedproteins
AT daileysimonc evolutionofependyminrelatedproteins
AT somorjaiildikoml evolutionofependyminrelatedproteins
AT cumminsscottf evolutionofependyminrelatedproteins
AT degnanbernardm evolutionofependyminrelatedproteins