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Genetic variants of the unsaturated fatty acid receptor GPR120 relating to obesity in dogs
G protein-coupled receptor (GPR) 120 is an unsaturated fatty acid receptor, which is associated with various physiological functions. It is reported that the genetic variant of GPR120, p.Arg270His, is detected more in obese people, and this genetic variation functionally relates to obesity in humans...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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The Japanese Society of Veterinary Science
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4638284/ https://www.ncbi.nlm.nih.gov/pubmed/25960032 http://dx.doi.org/10.1292/jvms.15-0031 |
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author | MIYABE, Masahiro GIN, Azusa ONOZAWA, Eri DAIMON, Mana YAMADA, Hana ODA, Hitomi MORI, Akihiro MOMOTA, Yutaka AZAKAMI, Daigo YAMAMOTO, Ichiro MOCHIZUKI, Mariko SAKO, Toshinori TAMURA, Katsutoshi ISHIOKA, Katsumi |
author_facet | MIYABE, Masahiro GIN, Azusa ONOZAWA, Eri DAIMON, Mana YAMADA, Hana ODA, Hitomi MORI, Akihiro MOMOTA, Yutaka AZAKAMI, Daigo YAMAMOTO, Ichiro MOCHIZUKI, Mariko SAKO, Toshinori TAMURA, Katsutoshi ISHIOKA, Katsumi |
author_sort | MIYABE, Masahiro |
collection | PubMed |
description | G protein-coupled receptor (GPR) 120 is an unsaturated fatty acid receptor, which is associated with various physiological functions. It is reported that the genetic variant of GPR120, p.Arg270His, is detected more in obese people, and this genetic variation functionally relates to obesity in humans. Obesity is a common nutritional disorder also in dogs, but the genetic factors have not ever been identified in dogs. In this study, we investigated the molecular structure of canine GPR120 and searched for candidate genetic variants which may relate to obesity in dogs. Canine GPR120 was highly homologous to those of other species, and seven transmembrane domains and two N-glycosylation sites were conserved. GPR120 mRNA was expressed in lung, jejunum, ileum, colon, hypothalamus, hippocampus, spinal cord, bone marrow, dermis and white adipose tissues in dogs, as those in mice and humans. Genetic variants of GPR120 were explored in client-owned 141 dogs, resulting in that 5 synonymous and 4 non-synonymous variants were found. The variant c.595C>A (p.Pro199Thr) was found in 40 dogs, and the gene frequency was significantly higher in dogs with higher body condition scores, i.e. 0.320 in BCS4–5 dogs, 0.175 in BCS3 dogs and 0.000 in BCS2 dogs. We conclude that c.595C>A (p.Pro199Thr) is a candidate variant relating to obesity, which may be helpful for nutritional management of dogs. |
format | Online Article Text |
id | pubmed-4638284 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | The Japanese Society of Veterinary Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-46382842015-11-10 Genetic variants of the unsaturated fatty acid receptor GPR120 relating to obesity in dogs MIYABE, Masahiro GIN, Azusa ONOZAWA, Eri DAIMON, Mana YAMADA, Hana ODA, Hitomi MORI, Akihiro MOMOTA, Yutaka AZAKAMI, Daigo YAMAMOTO, Ichiro MOCHIZUKI, Mariko SAKO, Toshinori TAMURA, Katsutoshi ISHIOKA, Katsumi J Vet Med Sci Internal Medicine G protein-coupled receptor (GPR) 120 is an unsaturated fatty acid receptor, which is associated with various physiological functions. It is reported that the genetic variant of GPR120, p.Arg270His, is detected more in obese people, and this genetic variation functionally relates to obesity in humans. Obesity is a common nutritional disorder also in dogs, but the genetic factors have not ever been identified in dogs. In this study, we investigated the molecular structure of canine GPR120 and searched for candidate genetic variants which may relate to obesity in dogs. Canine GPR120 was highly homologous to those of other species, and seven transmembrane domains and two N-glycosylation sites were conserved. GPR120 mRNA was expressed in lung, jejunum, ileum, colon, hypothalamus, hippocampus, spinal cord, bone marrow, dermis and white adipose tissues in dogs, as those in mice and humans. Genetic variants of GPR120 were explored in client-owned 141 dogs, resulting in that 5 synonymous and 4 non-synonymous variants were found. The variant c.595C>A (p.Pro199Thr) was found in 40 dogs, and the gene frequency was significantly higher in dogs with higher body condition scores, i.e. 0.320 in BCS4–5 dogs, 0.175 in BCS3 dogs and 0.000 in BCS2 dogs. We conclude that c.595C>A (p.Pro199Thr) is a candidate variant relating to obesity, which may be helpful for nutritional management of dogs. The Japanese Society of Veterinary Science 2015-05-10 2015-10 /pmc/articles/PMC4638284/ /pubmed/25960032 http://dx.doi.org/10.1292/jvms.15-0031 Text en ©2015 The Japanese Society of Veterinary Science http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives (by-nc-nd) License. |
spellingShingle | Internal Medicine MIYABE, Masahiro GIN, Azusa ONOZAWA, Eri DAIMON, Mana YAMADA, Hana ODA, Hitomi MORI, Akihiro MOMOTA, Yutaka AZAKAMI, Daigo YAMAMOTO, Ichiro MOCHIZUKI, Mariko SAKO, Toshinori TAMURA, Katsutoshi ISHIOKA, Katsumi Genetic variants of the unsaturated fatty acid receptor GPR120 relating to obesity in dogs |
title | Genetic variants of the unsaturated fatty acid receptor GPR120 relating to
obesity in dogs |
title_full | Genetic variants of the unsaturated fatty acid receptor GPR120 relating to
obesity in dogs |
title_fullStr | Genetic variants of the unsaturated fatty acid receptor GPR120 relating to
obesity in dogs |
title_full_unstemmed | Genetic variants of the unsaturated fatty acid receptor GPR120 relating to
obesity in dogs |
title_short | Genetic variants of the unsaturated fatty acid receptor GPR120 relating to
obesity in dogs |
title_sort | genetic variants of the unsaturated fatty acid receptor gpr120 relating to
obesity in dogs |
topic | Internal Medicine |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4638284/ https://www.ncbi.nlm.nih.gov/pubmed/25960032 http://dx.doi.org/10.1292/jvms.15-0031 |
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