The repertoire of G‐protein‐coupled receptor variations in the Japanese population 54KJPN

G-protein-coupled receptors (GPCRs) are the largest superfamily in the human genome and the major targets for the market drugs. Recent massive genomics studies revealed numerous natural variations in the general population. 54KJPN is the most extensive Japanese population genomics study, curating the whole genome sequences from about 54,000 individuals. Here, by analyzing 390 non-olfactory GPCR genes in the 54KJPN dataset, we annotated 25,443 missense single-nucleotide variations. Among them, we found 120 major variations that appear with an allele frequency greater than 0.5, including variations that occurred on posttranslational modification sites. Structural alignment of GPCRs using the generic numbering system in the GPCRdb reveals enrichment of alterations in the conserved arginine residue within the DRY motif, which contributes to downstream G-protein signaling. A comparison with the worldwide 1000 Genomes Project (1KGP) dataset found 23 variations that were present exclusively in the 54KJPN dataset. This study will be the basis for future pharmacogenomics studies for the Japanese population.

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Publication Details

Journal
Genes to Cells
Published
2024-09-23
DOI
https://doi.org/10.1111/gtc.13164
Primary Topic
Receptor Mechanisms and Signaling
Type
article
Field-Weighted Citation Impact
0.00

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article

The repertoire of G‐protein‐coupled receptor variations in the Japanese population 54KJPN

Tatsuya Ikuta, Asuka Inoue, Riko Suzuki
Genes to Cells
Receptor Mechanisms and Signaling
article

The repertoire of G‐protein‐coupled receptor variations in the Japanese population 54KJPN

Tatsuya Ikuta, Asuka Inoue, Riko Suzuki
article en

Abstract

G-protein-coupled receptors (GPCRs) are the largest superfamily in the human genome and the major targets for the market drugs. Recent massive genomics studies revealed numerous natural variations in the general population. 54KJPN is the most extensive Japanese population genomics study, curating the whole genome sequences from about 54,000 individuals. Here, by analyzing 390 non-olfactory GPCR genes in the 54KJPN dataset, we annotated 25,443 missense single-nucleotide variations. Among them, we found 120 major variations that appear with an allele frequency greater than 0.5, including variations that occurred on posttranslational modification sites. Structural alignment of GPCRs using the generic numbering system in the GPCRdb reveals enrichment of alterations in the conserved arginine residue within the DRY motif, which contributes to downstream G-protein signaling. A comparison with the worldwide 1000 Genomes Project (1KGP) dataset found 23 variations that were present exclusively in the 54KJPN dataset. This study will be the basis for future pharmacogenomics studies for the Japanese population.

Genes to CellsVol. 29(11)
Tohoku University (JP), Kyoto University (JP), Kyoto Pharmaceutical University (JP)
Japan Agency for Medical Research and Development, Japan Society for the Promotion of Science, Japan Science and Technology Agency, Institute of Genetics
Openalex Percentile: Top 86%
Receptor Mechanisms and Signaling
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The repertoire of G‐protein‐coupled receptor variations in the Japanese population 54KJPN — Tatsuya Ikuta, Asuka Inoue, et al. · Genes to Cells (2024) | TGRS Research Map | TGRS