Discovery and computational exploration of SNPs in GNRHR gene and their influence on protein structure and function in Indian goat breeds

IF 1 Q4 GENETICS & HEREDITY
S.K. Saranya , Marykutty Thomas , T.V. Aravindakshan , R. Thirupathy Venkatachalapathy , Jinty Sukumaran , Raji Kanakkaparambil
{"title":"Discovery and computational exploration of SNPs in GNRHR gene and their influence on protein structure and function in Indian goat breeds","authors":"S.K. Saranya ,&nbsp;Marykutty Thomas ,&nbsp;T.V. Aravindakshan ,&nbsp;R. Thirupathy Venkatachalapathy ,&nbsp;Jinty Sukumaran ,&nbsp;Raji Kanakkaparambil","doi":"10.1016/j.genrep.2024.102014","DOIUrl":null,"url":null,"abstract":"<div><p>This study focuses on identifying functional single nucleotide polymorphisms (SNPs) within the <em>gonadotropin-releasing hormone receptor (GNRHR) gene</em> and conducting subsequent <em>in-silico</em> analysis of their effects on protein structure and function in two distinct South Indian goat breeds, namely Attapady Black (<em>n</em> = 120) and Malabari goats (<em>n</em> = 180), known for their divergent prolificacy traits. Utilizing a DNA pool sequencing assay, ten SNPs were uncovered in the study population: c.-1129T&gt;G, c.-1069A&gt;G, c.-978A&gt;C, c.-605A&gt;G, c.-33A&gt;G, c.-29T&gt;G, c.48G&gt;A, c.75G&gt;A, c.209T&gt;G, and c.*212A&gt;G. Notably, two polymorphisms, c.-1129T&gt;G and c.-33A&gt;G, were novel. Additionally, two polymorphisms, c.-33A&gt;G and c.-978A&gt;C, were exclusive to Malabari goats. Analysis of upstream variants revealed modifications to transcription factor and micro-RNA (miRNA) binding sites, suggesting potential alterations in <em>GNRHR</em> expression. Of particular significance was the non-synonymous exonic variant at c.209T&gt;G locus, resulting in methionine to arginine substitution at the 70<sup>th</sup> position within the first intracellular loop of the receptor protein. This amino acid change may have implications for the functional dynamics of the receptor as GnRHR intracellular loops are involved in G protein coupling thereby facilitation of downstream signalling pathways. The identified SNPs and their <em>in-silico</em> impact analysis contribute to our understanding of the molecular mechanisms underlying reproductive traits in these goat populations, with implications for future breeding strategies and genomic selection programs.</p></div>","PeriodicalId":12673,"journal":{"name":"Gene Reports","volume":"37 ","pages":"Article 102014"},"PeriodicalIF":1.0000,"publicationDate":"2024-08-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Gene Reports","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2452014424001377","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"GENETICS & HEREDITY","Score":null,"Total":0}
引用次数: 0

Abstract

This study focuses on identifying functional single nucleotide polymorphisms (SNPs) within the gonadotropin-releasing hormone receptor (GNRHR) gene and conducting subsequent in-silico analysis of their effects on protein structure and function in two distinct South Indian goat breeds, namely Attapady Black (n = 120) and Malabari goats (n = 180), known for their divergent prolificacy traits. Utilizing a DNA pool sequencing assay, ten SNPs were uncovered in the study population: c.-1129T>G, c.-1069A>G, c.-978A>C, c.-605A>G, c.-33A>G, c.-29T>G, c.48G>A, c.75G>A, c.209T>G, and c.*212A>G. Notably, two polymorphisms, c.-1129T>G and c.-33A>G, were novel. Additionally, two polymorphisms, c.-33A>G and c.-978A>C, were exclusive to Malabari goats. Analysis of upstream variants revealed modifications to transcription factor and micro-RNA (miRNA) binding sites, suggesting potential alterations in GNRHR expression. Of particular significance was the non-synonymous exonic variant at c.209T>G locus, resulting in methionine to arginine substitution at the 70th position within the first intracellular loop of the receptor protein. This amino acid change may have implications for the functional dynamics of the receptor as GnRHR intracellular loops are involved in G protein coupling thereby facilitation of downstream signalling pathways. The identified SNPs and their in-silico impact analysis contribute to our understanding of the molecular mechanisms underlying reproductive traits in these goat populations, with implications for future breeding strategies and genomic selection programs.

印度山羊品种中 GNRHR 基因 SNPs 的发现和计算探索及其对蛋白质结构和功能的影响
本研究的重点是鉴定促性腺激素释放激素受体(GNRHR)基因中的功能性单核苷酸多态性(SNPs),并随后在两个不同的南印度山羊品种(即阿塔帕迪黑山羊(n = 120)和马拉巴里山羊(n = 180))中对它们对蛋白质结构和功能的影响进行了内部分析。利用 DNA 池测序法,在研究群体中发现了十个 SNPs:c.-1129T>G、c.-1069A>G、c.-978A>C、c.-605A>G、c.-33值得注意的是,c.-1129T>G 和 c.-33A>G 这两个多态性是新的。此外,两个多态性(c.-33A>G 和 c.-978A>C)是马拉巴里山羊独有的。对上游变异的分析表明,转录因子和微 RNA(miRNA)结合位点发生了改变,这表明 GNRHR 的表达可能发生了变化。特别重要的是位于c.209T>G位点的非同义外显子变异,它导致受体蛋白第一个细胞内环第70位的蛋氨酸被精氨酸取代。由于 GnRHR 细胞内环参与 G 蛋白耦合,从而促进下游信号通路,因此这一氨基酸变化可能会对受体的功能动态产生影响。鉴定出的 SNPs 及其内部影响分析有助于我们了解这些山羊种群生殖性状的分子机制,对未来的育种策略和基因组选择计划具有重要意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Gene Reports
Gene Reports Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
3.30
自引率
7.70%
发文量
246
审稿时长
49 days
期刊介绍: Gene Reports publishes papers that focus on the regulation, expression, function and evolution of genes in all biological contexts, including all prokaryotic and eukaryotic organisms, as well as viruses. Gene Reports strives to be a very diverse journal and topics in all fields will be considered for publication. Although not limited to the following, some general topics include: DNA Organization, Replication & Evolution -Focus on genomic DNA (chromosomal organization, comparative genomics, DNA replication, DNA repair, mobile DNA, mitochondrial DNA, chloroplast DNA). Expression & Function - Focus on functional RNAs (microRNAs, tRNAs, rRNAs, mRNA splicing, alternative polyadenylation) Regulation - Focus on processes that mediate gene-read out (epigenetics, chromatin, histone code, transcription, translation, protein degradation). Cell Signaling - Focus on mechanisms that control information flow into the nucleus to control gene expression (kinase and phosphatase pathways controlled by extra-cellular ligands, Wnt, Notch, TGFbeta/BMPs, FGFs, IGFs etc.) Profiling of gene expression and genetic variation - Focus on high throughput approaches (e.g., DeepSeq, ChIP-Seq, Affymetrix microarrays, proteomics) that define gene regulatory circuitry, molecular pathways and protein/protein networks. Genetics - Focus on development in model organisms (e.g., mouse, frog, fruit fly, worm), human genetic variation, population genetics, as well as agricultural and veterinary genetics. Molecular Pathology & Regenerative Medicine - Focus on the deregulation of molecular processes in human diseases and mechanisms supporting regeneration of tissues through pluripotent or multipotent stem cells.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信