Papers

Peer-reviewed
Oct, 2015

Genetic variants of the unsaturated fatty acid receptor GPR120 relating to obesity in dogs

JOURNAL OF VETERINARY MEDICAL SCIENCE
  • Masahiro Miyabe
  • Azusa Gin
  • Eri Onozawa
  • Mana Daimon
  • Hana Yamada
  • Hitomi Oda
  • Akihiro Mori
  • Yutaka Momota
  • Daigo Azakami
  • Ichiro Yamamoto
  • Mariko Mochizuki
  • Toshinori Sako
  • Katsutoshi Tamura
  • Katsumi Ishioka
  • Display all

Volume
77
Number
10
First page
1201
Last page
1206
Language
English
Publishing type
Research paper (scientific journal)
DOI
10.1292/jvms.15-0031
Publisher
JAPAN SOC VET SCI

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.

Link information
DOI
https://doi.org/10.1292/jvms.15-0031
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/25960032
Web of Science
https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=JSTA_CEL&SrcApp=J_Gate_JST&DestLinkType=FullRecord&KeyUT=WOS:000363831100002&DestApp=WOS_CPL
ID information
  • DOI : 10.1292/jvms.15-0031
  • ISSN : 0916-7250
  • eISSN : 1347-7439
  • Pubmed ID : 25960032
  • Web of Science ID : WOS:000363831100002

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