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Discovery of sea urchin NGFFFamide receptor unites a bilaterian neuropeptide family
Neuropeptides are ancient regulators of physiology and behaviour, but reconstruction of neuropeptide evolution is often difficult owing to lack of sequence conservation. Here, we report that the receptor for the neuropeptide NGFFFamide in the sea urchin Strongylocentrotus purpuratus (phylum Echinode...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4422128/ https://www.ncbi.nlm.nih.gov/pubmed/25904544 http://dx.doi.org/10.1098/rsob.150030 |
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author | Semmens, Dean C. Beets, Isabel Rowe, Matthew L. Blowes, Liisa M. Oliveri, Paola Elphick, Maurice R. |
author_facet | Semmens, Dean C. Beets, Isabel Rowe, Matthew L. Blowes, Liisa M. Oliveri, Paola Elphick, Maurice R. |
author_sort | Semmens, Dean C. |
collection | PubMed |
description | Neuropeptides are ancient regulators of physiology and behaviour, but reconstruction of neuropeptide evolution is often difficult owing to lack of sequence conservation. Here, we report that the receptor for the neuropeptide NGFFFamide in the sea urchin Strongylocentrotus purpuratus (phylum Echinodermata) is an orthologue of vertebrate neuropeptide-S (NPS) receptors and crustacean cardioactive peptide (CCAP) receptors. Importantly, this has facilitated reconstruction of the evolution of two bilaterian neuropeptide signalling systems. Genes encoding the precursor of a vasopressin/oxytocin-type neuropeptide and its receptor duplicated in a common ancestor of the Bilateria. One copy of the precursor retained ancestral features, as seen in highly conserved vasopressin/oxytocin–neurophysin-type precursors. The other copy diverged, but this took different courses in protostomes and deuterostomes. In protostomes, the occurrence of a disulfide bridge in neuropeptide product(s) of the precursor was retained, as in CCAP, but with loss of the neurophysin domain. In deuterostomes, we see the opposite scenario—the neuropeptides lost the disulfide bridge, and neurophysin was retained (as in the NGFFFamide precursor) but was subsequently lost in vertebrate NPS precursors. Thus, the sea urchin NGFFFamide precursor and receptor are ‘missing links’ in the evolutionary history of neuropeptides that control ecdysis in arthropods (CCAP) and regulate anxiety in humans (NPS). |
format | Online Article Text |
id | pubmed-4422128 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | The Royal Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-44221282015-05-18 Discovery of sea urchin NGFFFamide receptor unites a bilaterian neuropeptide family Semmens, Dean C. Beets, Isabel Rowe, Matthew L. Blowes, Liisa M. Oliveri, Paola Elphick, Maurice R. Open Biol Research Neuropeptides are ancient regulators of physiology and behaviour, but reconstruction of neuropeptide evolution is often difficult owing to lack of sequence conservation. Here, we report that the receptor for the neuropeptide NGFFFamide in the sea urchin Strongylocentrotus purpuratus (phylum Echinodermata) is an orthologue of vertebrate neuropeptide-S (NPS) receptors and crustacean cardioactive peptide (CCAP) receptors. Importantly, this has facilitated reconstruction of the evolution of two bilaterian neuropeptide signalling systems. Genes encoding the precursor of a vasopressin/oxytocin-type neuropeptide and its receptor duplicated in a common ancestor of the Bilateria. One copy of the precursor retained ancestral features, as seen in highly conserved vasopressin/oxytocin–neurophysin-type precursors. The other copy diverged, but this took different courses in protostomes and deuterostomes. In protostomes, the occurrence of a disulfide bridge in neuropeptide product(s) of the precursor was retained, as in CCAP, but with loss of the neurophysin domain. In deuterostomes, we see the opposite scenario—the neuropeptides lost the disulfide bridge, and neurophysin was retained (as in the NGFFFamide precursor) but was subsequently lost in vertebrate NPS precursors. Thus, the sea urchin NGFFFamide precursor and receptor are ‘missing links’ in the evolutionary history of neuropeptides that control ecdysis in arthropods (CCAP) and regulate anxiety in humans (NPS). The Royal Society 2015-04-22 /pmc/articles/PMC4422128/ /pubmed/25904544 http://dx.doi.org/10.1098/rsob.150030 Text en http://creativecommons.org/licenses/by/4.0/ © 2015 The Authors. Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, provided the original author and source are credited. |
spellingShingle | Research Semmens, Dean C. Beets, Isabel Rowe, Matthew L. Blowes, Liisa M. Oliveri, Paola Elphick, Maurice R. Discovery of sea urchin NGFFFamide receptor unites a bilaterian neuropeptide family |
title | Discovery of sea urchin NGFFFamide receptor unites a bilaterian neuropeptide family |
title_full | Discovery of sea urchin NGFFFamide receptor unites a bilaterian neuropeptide family |
title_fullStr | Discovery of sea urchin NGFFFamide receptor unites a bilaterian neuropeptide family |
title_full_unstemmed | Discovery of sea urchin NGFFFamide receptor unites a bilaterian neuropeptide family |
title_short | Discovery of sea urchin NGFFFamide receptor unites a bilaterian neuropeptide family |
title_sort | discovery of sea urchin ngfffamide receptor unites a bilaterian neuropeptide family |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4422128/ https://www.ncbi.nlm.nih.gov/pubmed/25904544 http://dx.doi.org/10.1098/rsob.150030 |
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