3个马品种间IHH基因多态性及其在骨软骨病马关联检测中的应用

IF 2.1 3区 生物学 Q3 GENETICS & HEREDITY
T. Zabek, P. Golonka, A. Fornal, E. Semik
{"title":"3个马品种间IHH基因多态性及其在骨软骨病马关联检测中的应用","authors":"T. Zabek,&nbsp;P. Golonka,&nbsp;A. Fornal,&nbsp;E. Semik","doi":"10.1111/j.1601-5223.2013.02282.x","DOIUrl":null,"url":null,"abstract":"<p>Genetic polymorphism of <i>IHH</i> gene were investigated in Angloarabian, Polish Coldblood and Polish Halfbred horses with the inclusion of a group of Polish Halfbreds affected by osteochondrosis. <i>IHH</i> is a good candidate gene for association study of developmental disorders mainly affecting skeleton development. DNA sequence spanning <i>IHH</i> gene annotated in the horse genome and its putative promoter were investigated using SANGER sequencing. Analysis of genetic variability at polymorphic sites in the <i>IHH</i> gene body and the promoter region confirmed genetic differences between warmblood and coldblood horse breeds. A test for allelic and genotypic association at particular SNP sites revealed no association with osteochondrosis in investigated group of Polish Halfbreds. It was concluded that participation of different warmblood breeds in pedigrees of Polish Halfbreds make it difficult to search for genetic variants being associated with this complex disorder in this breed. <i>IHH</i> gene polymorphism investigated among three different horse populations would be valuable for further studies on equine bone developmental disorders.</p>","PeriodicalId":55057,"journal":{"name":"Hereditas","volume":null,"pages":null},"PeriodicalIF":2.1000,"publicationDate":"2013-07-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1111/j.1601-5223.2013.02282.x","citationCount":"5","resultStr":"{\"title\":\"IHH gene polymorphism among three horse breeds and its application for association test in horses with osteochondrosis\",\"authors\":\"T. Zabek,&nbsp;P. Golonka,&nbsp;A. Fornal,&nbsp;E. Semik\",\"doi\":\"10.1111/j.1601-5223.2013.02282.x\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>Genetic polymorphism of <i>IHH</i> gene were investigated in Angloarabian, Polish Coldblood and Polish Halfbred horses with the inclusion of a group of Polish Halfbreds affected by osteochondrosis. <i>IHH</i> is a good candidate gene for association study of developmental disorders mainly affecting skeleton development. DNA sequence spanning <i>IHH</i> gene annotated in the horse genome and its putative promoter were investigated using SANGER sequencing. Analysis of genetic variability at polymorphic sites in the <i>IHH</i> gene body and the promoter region confirmed genetic differences between warmblood and coldblood horse breeds. A test for allelic and genotypic association at particular SNP sites revealed no association with osteochondrosis in investigated group of Polish Halfbreds. It was concluded that participation of different warmblood breeds in pedigrees of Polish Halfbreds make it difficult to search for genetic variants being associated with this complex disorder in this breed. <i>IHH</i> gene polymorphism investigated among three different horse populations would be valuable for further studies on equine bone developmental disorders.</p>\",\"PeriodicalId\":55057,\"journal\":{\"name\":\"Hereditas\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":2.1000,\"publicationDate\":\"2013-07-08\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1111/j.1601-5223.2013.02282.x\",\"citationCount\":\"5\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Hereditas\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1111/j.1601-5223.2013.02282.x\",\"RegionNum\":3,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"GENETICS & HEREDITY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Hereditas","FirstCategoryId":"99","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1111/j.1601-5223.2013.02282.x","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"GENETICS & HEREDITY","Score":null,"Total":0}
引用次数: 5

摘要

研究了盎格鲁阿拉伯马、波兰冷血马和波兰半种马的IHH基因多态性,其中包括一组受骨软骨病影响的波兰半种马。IHH是主要影响骨骼发育的发育障碍关联研究的良好候选基因。利用SANGER测序技术研究了马基因组中跨越IHH基因注释的DNA序列及其可能的启动子。对IHH基因体多态性位点和启动子区域的遗传变异分析证实了温血马和冷血马品种之间的遗传差异。对特定SNP位点的等位基因和基因型关联的测试显示,在调查的波兰混血儿群体中,与骨软骨病没有关联。结论是,不同温血品种在波兰混血儿谱系中的参与使得在该品种中寻找与这种复杂疾病相关的遗传变异变得困难。通过对三个不同马种群间IHH基因多态性的研究,对进一步研究马骨发育障碍具有重要意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

IHH gene polymorphism among three horse breeds and its application for association test in horses with osteochondrosis

IHH gene polymorphism among three horse breeds and its application for association test in horses with osteochondrosis

Genetic polymorphism of IHH gene were investigated in Angloarabian, Polish Coldblood and Polish Halfbred horses with the inclusion of a group of Polish Halfbreds affected by osteochondrosis. IHH is a good candidate gene for association study of developmental disorders mainly affecting skeleton development. DNA sequence spanning IHH gene annotated in the horse genome and its putative promoter were investigated using SANGER sequencing. Analysis of genetic variability at polymorphic sites in the IHH gene body and the promoter region confirmed genetic differences between warmblood and coldblood horse breeds. A test for allelic and genotypic association at particular SNP sites revealed no association with osteochondrosis in investigated group of Polish Halfbreds. It was concluded that participation of different warmblood breeds in pedigrees of Polish Halfbreds make it difficult to search for genetic variants being associated with this complex disorder in this breed. IHH gene polymorphism investigated among three different horse populations would be valuable for further studies on equine bone developmental disorders.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Hereditas
Hereditas 生物-遗传学
CiteScore
4.30
自引率
3.70%
发文量
46
审稿时长
6 weeks
期刊介绍: For almost a century, Hereditas has published original cutting-edge research and reviews. As the Official journal of the Mendelian Society of Lund, the journal welcomes research from across all areas of genetics and genomics. Topics of interest include human and medical genetics, animal and plant genetics, microbial genetics, agriculture and bioinformatics.
×
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