Xiaoxi Liu , Stanislav Cherepanov , Mehdi Abouzari , Amila Zuko , Shu Yang , Jamasb Sayadi , Xiaoyuan Jia , Chikashi Terao , Tsukasa Sasaki , Shigeru Yokoyama
{"title":"人类催产素受体的 R150S 突变:功能增益效应及其对自闭症谱系障碍的影响","authors":"Xiaoxi Liu , Stanislav Cherepanov , Mehdi Abouzari , Amila Zuko , Shu Yang , Jamasb Sayadi , Xiaoyuan Jia , Chikashi Terao , Tsukasa Sasaki , Shigeru Yokoyama","doi":"10.1016/j.peptides.2024.171301","DOIUrl":null,"url":null,"abstract":"<div><div>This study investigates the rs547238576 (R150S) missense variant in the oxytocin receptor (<em>OXTR</em>) gene, previously observed through screening of rare variants in Japanese individuals with autism spectrum disorders (ASD). Contrary to the anticipated loss-of-function, R150S exhibits gain-of-function effects, enhancing oxytocin (OXT) sensitivity, ligand-binding affinity, and OXT-induced Ca<sup>2+</sup> mobilization <em>in vitro</em>. This suggests R150S may alter OXT signaling, potentially contributing to the excitatory/inhibitory imbalance seen in ASD and other psychiatric disorders. Our findings underscore the significance of genetic variations in <em>OXTR</em> on functional activity and highlight the necessity for population-specific genetic study and <em>in vitro</em> analysis to elucidate genetic susceptibilities to neuropsychiatric conditions.</div></div>","PeriodicalId":19765,"journal":{"name":"Peptides","volume":null,"pages":null},"PeriodicalIF":2.8000,"publicationDate":"2024-10-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"R150S mutation in the human oxytocin receptor: Gain-of-function effects and implication in autism spectrum disorder\",\"authors\":\"Xiaoxi Liu , Stanislav Cherepanov , Mehdi Abouzari , Amila Zuko , Shu Yang , Jamasb Sayadi , Xiaoyuan Jia , Chikashi Terao , Tsukasa Sasaki , Shigeru Yokoyama\",\"doi\":\"10.1016/j.peptides.2024.171301\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>This study investigates the rs547238576 (R150S) missense variant in the oxytocin receptor (<em>OXTR</em>) gene, previously observed through screening of rare variants in Japanese individuals with autism spectrum disorders (ASD). Contrary to the anticipated loss-of-function, R150S exhibits gain-of-function effects, enhancing oxytocin (OXT) sensitivity, ligand-binding affinity, and OXT-induced Ca<sup>2+</sup> mobilization <em>in vitro</em>. This suggests R150S may alter OXT signaling, potentially contributing to the excitatory/inhibitory imbalance seen in ASD and other psychiatric disorders. Our findings underscore the significance of genetic variations in <em>OXTR</em> on functional activity and highlight the necessity for population-specific genetic study and <em>in vitro</em> analysis to elucidate genetic susceptibilities to neuropsychiatric conditions.</div></div>\",\"PeriodicalId\":19765,\"journal\":{\"name\":\"Peptides\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":2.8000,\"publicationDate\":\"2024-10-10\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Peptides\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0196978124001542\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"BIOCHEMISTRY & MOLECULAR BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Peptides","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0196978124001542","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
R150S mutation in the human oxytocin receptor: Gain-of-function effects and implication in autism spectrum disorder
This study investigates the rs547238576 (R150S) missense variant in the oxytocin receptor (OXTR) gene, previously observed through screening of rare variants in Japanese individuals with autism spectrum disorders (ASD). Contrary to the anticipated loss-of-function, R150S exhibits gain-of-function effects, enhancing oxytocin (OXT) sensitivity, ligand-binding affinity, and OXT-induced Ca2+ mobilization in vitro. This suggests R150S may alter OXT signaling, potentially contributing to the excitatory/inhibitory imbalance seen in ASD and other psychiatric disorders. Our findings underscore the significance of genetic variations in OXTR on functional activity and highlight the necessity for population-specific genetic study and in vitro analysis to elucidate genetic susceptibilities to neuropsychiatric conditions.
期刊介绍:
Peptides is an international journal presenting original contributions on the biochemistry, physiology and pharmacology of biological active peptides, as well as their functions that relate to gastroenterology, endocrinology, and behavioral effects.
Peptides emphasizes all aspects of high profile peptide research in mammals and non-mammalian vertebrates. Special consideration can be given to plants and invertebrates. Submission of articles with clinical relevance is particularly encouraged.