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The Evolution and Variety of RFamide-Type Neuropeptides: Insights from Deuterostomian Invertebrates
Five families of neuropeptides that have a C-terminal RFamide motif have been identified in vertebrates: (1) gonadotropin-inhibitory hormone (GnIH), (2) neuropeptide FF (NPFF), (3) pyroglutamylated RFamide peptide (QRFP), (4) prolactin-releasing peptide (PrRP), and (5) Kisspeptin. Experimental demon...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2014
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4062910/ https://www.ncbi.nlm.nih.gov/pubmed/24994999 http://dx.doi.org/10.3389/fendo.2014.00093 |
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author | Elphick, Maurice R. Mirabeau, Olivier |
author_facet | Elphick, Maurice R. Mirabeau, Olivier |
author_sort | Elphick, Maurice R. |
collection | PubMed |
description | Five families of neuropeptides that have a C-terminal RFamide motif have been identified in vertebrates: (1) gonadotropin-inhibitory hormone (GnIH), (2) neuropeptide FF (NPFF), (3) pyroglutamylated RFamide peptide (QRFP), (4) prolactin-releasing peptide (PrRP), and (5) Kisspeptin. Experimental demonstration of neuropeptide–receptor pairings combined with comprehensive analysis of genomic and/or transcriptomic sequence data indicate that, with the exception of the deuterostomian PrRP system, the evolutionary origins of these neuropeptides can be traced back to the common ancestor of bilaterians. Here, we review the occurrence of homologs of vertebrate RFamide-type neuropeptides and their receptors in deuterostomian invertebrates – urochordates, cephalochordates, hemichordates, and echinoderms. Extending analysis of the occurrence of the RFamide motif in other bilaterian neuropeptide families reveals RFamide-type peptides that have acquired modified C-terminal characteristics in the vertebrate lineage (e.g., NPY/NPF), neuropeptide families where the RFamide motif is unique to protostomian members (e.g., CCK/sulfakinins), and RFamide-type peptides that have been lost in the vertebrate lineage (e.g., luqins). Furthermore, the RFamide motif is also a feature of neuropeptide families with a more restricted phylogenetic distribution (e.g., the prototypical FMRFamide-related neuropeptides in protostomes). Thus, the RFamide motif is both an ancient and a convergent feature of neuropeptides, with conservation, acquisition, or loss of this motif occurring in different branches of the animal kingdom. |
format | Online Article Text |
id | pubmed-4062910 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-40629102014-07-03 The Evolution and Variety of RFamide-Type Neuropeptides: Insights from Deuterostomian Invertebrates Elphick, Maurice R. Mirabeau, Olivier Front Endocrinol (Lausanne) Endocrinology Five families of neuropeptides that have a C-terminal RFamide motif have been identified in vertebrates: (1) gonadotropin-inhibitory hormone (GnIH), (2) neuropeptide FF (NPFF), (3) pyroglutamylated RFamide peptide (QRFP), (4) prolactin-releasing peptide (PrRP), and (5) Kisspeptin. Experimental demonstration of neuropeptide–receptor pairings combined with comprehensive analysis of genomic and/or transcriptomic sequence data indicate that, with the exception of the deuterostomian PrRP system, the evolutionary origins of these neuropeptides can be traced back to the common ancestor of bilaterians. Here, we review the occurrence of homologs of vertebrate RFamide-type neuropeptides and their receptors in deuterostomian invertebrates – urochordates, cephalochordates, hemichordates, and echinoderms. Extending analysis of the occurrence of the RFamide motif in other bilaterian neuropeptide families reveals RFamide-type peptides that have acquired modified C-terminal characteristics in the vertebrate lineage (e.g., NPY/NPF), neuropeptide families where the RFamide motif is unique to protostomian members (e.g., CCK/sulfakinins), and RFamide-type peptides that have been lost in the vertebrate lineage (e.g., luqins). Furthermore, the RFamide motif is also a feature of neuropeptide families with a more restricted phylogenetic distribution (e.g., the prototypical FMRFamide-related neuropeptides in protostomes). Thus, the RFamide motif is both an ancient and a convergent feature of neuropeptides, with conservation, acquisition, or loss of this motif occurring in different branches of the animal kingdom. Frontiers Media S.A. 2014-06-19 /pmc/articles/PMC4062910/ /pubmed/24994999 http://dx.doi.org/10.3389/fendo.2014.00093 Text en Copyright © 2014 Elphick and Mirabeau. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Endocrinology Elphick, Maurice R. Mirabeau, Olivier The Evolution and Variety of RFamide-Type Neuropeptides: Insights from Deuterostomian Invertebrates |
title | The Evolution and Variety of RFamide-Type Neuropeptides: Insights from Deuterostomian Invertebrates |
title_full | The Evolution and Variety of RFamide-Type Neuropeptides: Insights from Deuterostomian Invertebrates |
title_fullStr | The Evolution and Variety of RFamide-Type Neuropeptides: Insights from Deuterostomian Invertebrates |
title_full_unstemmed | The Evolution and Variety of RFamide-Type Neuropeptides: Insights from Deuterostomian Invertebrates |
title_short | The Evolution and Variety of RFamide-Type Neuropeptides: Insights from Deuterostomian Invertebrates |
title_sort | evolution and variety of rfamide-type neuropeptides: insights from deuterostomian invertebrates |
topic | Endocrinology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4062910/ https://www.ncbi.nlm.nih.gov/pubmed/24994999 http://dx.doi.org/10.3389/fendo.2014.00093 |
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