Sequence polymorphisms provide a common consensus sequence for GPR41 and GPR42
- PMID: 19630535
- DOI: 10.1089/dna.2009.0916
Sequence polymorphisms provide a common consensus sequence for GPR41 and GPR42
Abstract
GPR41 and GPR42 are two closely related genes that are part of a cluster of four adjacent G protein-coupled receptors (GPCRs) (GPR40, 41, 42, and 43) localized on human chromosome 19. There are only six nucleotide and amino acid differences between GPR41 and GPR42. High sequence homology between these two genes suggests that they are the result of a recent duplication event. Mutagenesis studies have previously shown that amino acid 174 is important for functional signaling since conversion of R174 (found in GPR41) to W174 (found in GPR42) silences the response to short chain fatty acids, raising the possibility that GPR42 might be an inactive pseudogene. In the present study, we present evidence showing that the six amino acid differences, including that R/W174 are polymorphisms rather than gene-specific differences between GPR41 and GPR42. Most importantly, of the 202 GPR42 alleles that were genotyped, 123 (61%) had arginine at amino acid 174, suggesting that GPR42 could potentially be a functional gene in a significant fraction of the human population and should therefore not be categorically characterized as an inactive pseudogene. In addition, a second copy of GPR40 was found to localize between GPR41 and GPR42 genes in human and chimp, suggesting that the duplication event that generated GPR42 in human and chimp might have involved a 12.5 kb DNA fragment that also contains GPR40. This second copy of the GPR40 gene is a pseudogene since it has diverged extensively from GPR40 and does not contain an open reading frame.
Similar articles
-
Human GPR42 is a transcribed multisite variant that exhibits copy number polymorphism and is functional when heterologously expressed.Sci Rep. 2015 Aug 11;5:12880. doi: 10.1038/srep12880. Sci Rep. 2015. PMID: 26260360 Free PMC article.
-
A cluster of four novel human G protein-coupled receptor genes occurring in close proximity to CD22 gene on chromosome 19q13.1.Biochem Biophys Res Commun. 1997 Oct 20;239(2):543-7. doi: 10.1006/bbrc.1997.7513. Biochem Biophys Res Commun. 1997. PMID: 9344866
-
Identification and characterization of the bovine G protein-coupled receptor GPR41 and GPR43 genes.J Dairy Sci. 2009 Jun;92(6):2696-705. doi: 10.3168/jds.2009-2037. J Dairy Sci. 2009. PMID: 19448003
-
Regulation of the GPR40 locus: towards a molecular understanding.Biochem Soc Trans. 2008 Jun;36(Pt 3):360-2. doi: 10.1042/BST0360360. Biochem Soc Trans. 2008. PMID: 18481958 Review.
-
A family of fatty acid binding receptors.DNA Cell Biol. 2005 Jan;24(1):54-61. doi: 10.1089/dna.2005.24.54. DNA Cell Biol. 2005. PMID: 15684720 Review.
Cited by
-
From microbe to man: the role of microbial short chain fatty acid metabolites in host cell biology.Am J Physiol Cell Physiol. 2014 Dec 1;307(11):C979-85. doi: 10.1152/ajpcell.00228.2014. Epub 2014 Oct 1. Am J Physiol Cell Physiol. 2014. PMID: 25273884 Free PMC article. Review.
-
Agonism and allosterism: the pharmacology of the free fatty acid receptors FFA2 and FFA3.Br J Pharmacol. 2009 Sep;158(1):146-53. doi: 10.1111/j.1476-5381.2009.00421.x. Br J Pharmacol. 2009. PMID: 19719777 Free PMC article. Review.
-
The Concise Guide to PHARMACOLOGY 2013/14: G protein-coupled receptors.Br J Pharmacol. 2013 Dec;170(8):1459-581. doi: 10.1111/bph.12445. Br J Pharmacol. 2013. PMID: 24517644 Free PMC article.
-
Human GPR42 is a transcribed multisite variant that exhibits copy number polymorphism and is functional when heterologously expressed.Sci Rep. 2015 Aug 11;5:12880. doi: 10.1038/srep12880. Sci Rep. 2015. PMID: 26260360 Free PMC article.
-
Free Fatty Acid Receptors 2 and 3 as Microbial Metabolite Sensors to Shape Host Health: Pharmacophysiological View.Biomedicines. 2020 Jun 8;8(6):154. doi: 10.3390/biomedicines8060154. Biomedicines. 2020. PMID: 32521775 Free PMC article. Review.
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Molecular Biology Databases