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Unexpected multiplicity of QRFP receptors in early vertebrate evolution

The neuropeptide QRFP, also called 26RFa, and its G protein-coupled receptor GPR103 have been identified in all vertebrates investigated. In mammals, this peptide-receptor pair has been found to have several effects including stimulation of appetite. Recently, we reported that a QRFP peptide is pres...

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Autores principales: Larhammar, Dan, Xu, Bo, Bergqvist, Christina A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4208404/
https://www.ncbi.nlm.nih.gov/pubmed/25386115
http://dx.doi.org/10.3389/fnins.2014.00337
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author Larhammar, Dan
Xu, Bo
Bergqvist, Christina A.
author_facet Larhammar, Dan
Xu, Bo
Bergqvist, Christina A.
author_sort Larhammar, Dan
collection PubMed
description The neuropeptide QRFP, also called 26RFa, and its G protein-coupled receptor GPR103 have been identified in all vertebrates investigated. In mammals, this peptide-receptor pair has been found to have several effects including stimulation of appetite. Recently, we reported that a QRFP peptide is present in amphioxus, Branchiostoma floridae, and we also identified a QRFP receptor (QRFPR) that mediates a functional response to sub-nanomolar concentrations of the amphioxus peptide as well as short and long human QRFP (Xu et al., submitted). Because the ancestral vertebrate underwent two tetraploidizations, it might be expected that duplicates of the QRFP gene and its receptor gene may exist. Indeed, we report here the identification of multiple vertebrate QRFPR genes. Three QRFPR genes are present in the coelacanth Latimeria chalumnae, representing an early diverging sarcopterygian lineage. Three QRFPR genes are present in the basal actinopterygian fish, the spotted gar. Phylogenetic and chromosomal analyses show that only two of these receptor genes are orthologous between the two species, thus demonstrating a total of four distinct vertebrate genes. Three of the QRFPR genes resulted from the early vertebrate tetraploidizations and were copied along with syntenic neuropeptide Y receptor genes. The fourth QRFPR gene may be an even older and distinct lineage. Because mammals and birds have only a single QRFPR gene, this means that three genes have been lost in these lineages, and at least one of these was lost independently in mammals and birds because it is still present in a turtle. In conclusion, these results show that the QRFP system gained considerable complexity in the early stages of vertebrate evolution and still maintains much of this in some lineages, and that it has been secondarily reduced in mammals.
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spelling pubmed-42084042014-11-10 Unexpected multiplicity of QRFP receptors in early vertebrate evolution Larhammar, Dan Xu, Bo Bergqvist, Christina A. Front Neurosci Endocrinology The neuropeptide QRFP, also called 26RFa, and its G protein-coupled receptor GPR103 have been identified in all vertebrates investigated. In mammals, this peptide-receptor pair has been found to have several effects including stimulation of appetite. Recently, we reported that a QRFP peptide is present in amphioxus, Branchiostoma floridae, and we also identified a QRFP receptor (QRFPR) that mediates a functional response to sub-nanomolar concentrations of the amphioxus peptide as well as short and long human QRFP (Xu et al., submitted). Because the ancestral vertebrate underwent two tetraploidizations, it might be expected that duplicates of the QRFP gene and its receptor gene may exist. Indeed, we report here the identification of multiple vertebrate QRFPR genes. Three QRFPR genes are present in the coelacanth Latimeria chalumnae, representing an early diverging sarcopterygian lineage. Three QRFPR genes are present in the basal actinopterygian fish, the spotted gar. Phylogenetic and chromosomal analyses show that only two of these receptor genes are orthologous between the two species, thus demonstrating a total of four distinct vertebrate genes. Three of the QRFPR genes resulted from the early vertebrate tetraploidizations and were copied along with syntenic neuropeptide Y receptor genes. The fourth QRFPR gene may be an even older and distinct lineage. Because mammals and birds have only a single QRFPR gene, this means that three genes have been lost in these lineages, and at least one of these was lost independently in mammals and birds because it is still present in a turtle. In conclusion, these results show that the QRFP system gained considerable complexity in the early stages of vertebrate evolution and still maintains much of this in some lineages, and that it has been secondarily reduced in mammals. Frontiers Media S.A. 2014-10-24 /pmc/articles/PMC4208404/ /pubmed/25386115 http://dx.doi.org/10.3389/fnins.2014.00337 Text en Copyright © 2014 Larhammar, Xu and Bergqvist. http://creativecommons.org/licenses/by/4.0/ 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
Larhammar, Dan
Xu, Bo
Bergqvist, Christina A.
Unexpected multiplicity of QRFP receptors in early vertebrate evolution
title Unexpected multiplicity of QRFP receptors in early vertebrate evolution
title_full Unexpected multiplicity of QRFP receptors in early vertebrate evolution
title_fullStr Unexpected multiplicity of QRFP receptors in early vertebrate evolution
title_full_unstemmed Unexpected multiplicity of QRFP receptors in early vertebrate evolution
title_short Unexpected multiplicity of QRFP receptors in early vertebrate evolution
title_sort unexpected multiplicity of qrfp receptors in early vertebrate evolution
topic Endocrinology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4208404/
https://www.ncbi.nlm.nih.gov/pubmed/25386115
http://dx.doi.org/10.3389/fnins.2014.00337
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