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Evolution of complexity in the zebrafish synapse proteome
The proteome of human brain synapses is highly complex and is mutated in over 130 diseases. This complexity arose from two whole-genome duplications early in the vertebrate lineage. Zebrafish are used in modelling human diseases; however, its synapse proteome is uncharacterized, and whether the tele...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5337974/ https://www.ncbi.nlm.nih.gov/pubmed/28252024 http://dx.doi.org/10.1038/ncomms14613 |
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author | Bayés, Àlex Collins, Mark O. Reig-Viader, Rita Gou, Gemma Goulding, David Izquierdo, Abril Choudhary, Jyoti S. Emes, Richard D. Grant, Seth G. N. |
author_facet | Bayés, Àlex Collins, Mark O. Reig-Viader, Rita Gou, Gemma Goulding, David Izquierdo, Abril Choudhary, Jyoti S. Emes, Richard D. Grant, Seth G. N. |
author_sort | Bayés, Àlex |
collection | PubMed |
description | The proteome of human brain synapses is highly complex and is mutated in over 130 diseases. This complexity arose from two whole-genome duplications early in the vertebrate lineage. Zebrafish are used in modelling human diseases; however, its synapse proteome is uncharacterized, and whether the teleost-specific genome duplication (TSGD) influenced complexity is unknown. We report the characterization of the proteomes and ultrastructure of central synapses in zebrafish and analyse the importance of the TSGD. While the TSGD increases overall synapse proteome complexity, the postsynaptic density (PSD) proteome of zebrafish has lower complexity than mammals. A highly conserved set of ∼1,000 proteins is shared across vertebrates. PSD ultrastructural features are also conserved. Lineage-specific proteome differences indicate that vertebrate species evolved distinct synapse types and functions. The data sets are a resource for a wide range of studies and have important implications for the use of zebrafish in modelling human synaptic diseases. |
format | Online Article Text |
id | pubmed-5337974 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-53379742017-03-09 Evolution of complexity in the zebrafish synapse proteome Bayés, Àlex Collins, Mark O. Reig-Viader, Rita Gou, Gemma Goulding, David Izquierdo, Abril Choudhary, Jyoti S. Emes, Richard D. Grant, Seth G. N. Nat Commun Article The proteome of human brain synapses is highly complex and is mutated in over 130 diseases. This complexity arose from two whole-genome duplications early in the vertebrate lineage. Zebrafish are used in modelling human diseases; however, its synapse proteome is uncharacterized, and whether the teleost-specific genome duplication (TSGD) influenced complexity is unknown. We report the characterization of the proteomes and ultrastructure of central synapses in zebrafish and analyse the importance of the TSGD. While the TSGD increases overall synapse proteome complexity, the postsynaptic density (PSD) proteome of zebrafish has lower complexity than mammals. A highly conserved set of ∼1,000 proteins is shared across vertebrates. PSD ultrastructural features are also conserved. Lineage-specific proteome differences indicate that vertebrate species evolved distinct synapse types and functions. The data sets are a resource for a wide range of studies and have important implications for the use of zebrafish in modelling human synaptic diseases. Nature Publishing Group 2017-03-02 /pmc/articles/PMC5337974/ /pubmed/28252024 http://dx.doi.org/10.1038/ncomms14613 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Bayés, Àlex Collins, Mark O. Reig-Viader, Rita Gou, Gemma Goulding, David Izquierdo, Abril Choudhary, Jyoti S. Emes, Richard D. Grant, Seth G. N. Evolution of complexity in the zebrafish synapse proteome |
title | Evolution of complexity in the zebrafish synapse proteome |
title_full | Evolution of complexity in the zebrafish synapse proteome |
title_fullStr | Evolution of complexity in the zebrafish synapse proteome |
title_full_unstemmed | Evolution of complexity in the zebrafish synapse proteome |
title_short | Evolution of complexity in the zebrafish synapse proteome |
title_sort | evolution of complexity in the zebrafish synapse proteome |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5337974/ https://www.ncbi.nlm.nih.gov/pubmed/28252024 http://dx.doi.org/10.1038/ncomms14613 |
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