Cardiomyopathy associated 5 (CMYA5) implicated as a genetic risk factor for radial hemimelia in Siamese cats.

IF 1.9 2区 农林科学 Q2 VETERINARY SCIENCES
Nüket Bilgen, Bengi Çınar Kul, Mustafa Yenal Akkurt, Caner Bakıcı, Reuben M Buckley, Leslie A Lyons, Lyndon M Coghill, Özge Şebnem Çıldır, Furkan Kutlu
{"title":"<i>Cardiomyopathy associated 5</i> (<i>CMYA5</i>) implicated as a genetic risk factor for radial hemimelia in Siamese cats.","authors":"Nüket Bilgen, Bengi Çınar Kul, Mustafa Yenal Akkurt, Caner Bakıcı, Reuben M Buckley, Leslie A Lyons, Lyndon M Coghill, Özge Şebnem Çıldır, Furkan Kutlu","doi":"10.1177/1098612X231193557","DOIUrl":null,"url":null,"abstract":"<p><strong>Objectives: </strong>The present study aimed to determine the inheritance pattern and genetic cause of congenital radial hemimelia (RH) in cats.</p><p><strong>Methods: </strong>Clinical and genetic analyses were conducted on a Siamese cat family (n = 18), including two siblings with RH. Radiographs were obtained for the affected kittens and echocardiograms of an affected kitten and sire. Whole genome sequencing was completed on the two cases and the parents. Genomic data were compared with the 99 Lives Cat Genome data set of 420 additional domestic cats with whole genome and whole exome sequencing data. Variants were considered as homozygous in the two cases of the siblings with RH and heterozygous in the parents. Candidate variants were genotyped by Sanger sequencing in the extended pedigree.</p><p><strong>Results: </strong>Radiographs of the female kitten revealed bilateral absence of the radii and bowing of the humeri, while the male kitten showed a dysplastic right radius. Echocardiography suggested the female kitten had restrictive cardiomyopathy with a positive left atrial-to-aortic root ratio (LA:Ao = 1.83 cm), whereas hypertrophic cardiomyopathy was more likely in the sire, showing diastolic dysfunction using tissue Doppler imaging (59.06 cm/s). Twenty-two DNA variants were unique and homozygous in the affected kittens and heterozygous in the parents. Seven variants clustered in one chromosomal region, including two frameshift variants in <i>cardiomyopathy associated 5</i> (<i>CMYA5</i>) and five variants in <i>junction mediating and regulatory protein</i>, <i>P53 cofactor</i> (<i>JMY</i> ), including a missense and an in-frame deletion.</p><p><strong>Conclusions and relevance: </strong>The present study suggested an autosomal recessive mode of inheritance with variable expression for RH in the Siamese cat family. Candidate variants for the phenotype were identified, implicating their roles in bone development. These genes should be considered as potentially causal for other cats with RH. Siamese cat breeders should consider genetically testing their cats for these variants to prevent further dissemination of the suspected variants within the breed.</p>","PeriodicalId":15851,"journal":{"name":"Journal of Feline Medicine and Surgery","volume":null,"pages":null},"PeriodicalIF":1.9000,"publicationDate":"2023-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10812016/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Feline Medicine and Surgery","FirstCategoryId":"97","ListUrlMain":"https://doi.org/10.1177/1098612X231193557","RegionNum":2,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"VETERINARY SCIENCES","Score":null,"Total":0}
引用次数: 0

Abstract

Objectives: The present study aimed to determine the inheritance pattern and genetic cause of congenital radial hemimelia (RH) in cats.

Methods: Clinical and genetic analyses were conducted on a Siamese cat family (n = 18), including two siblings with RH. Radiographs were obtained for the affected kittens and echocardiograms of an affected kitten and sire. Whole genome sequencing was completed on the two cases and the parents. Genomic data were compared with the 99 Lives Cat Genome data set of 420 additional domestic cats with whole genome and whole exome sequencing data. Variants were considered as homozygous in the two cases of the siblings with RH and heterozygous in the parents. Candidate variants were genotyped by Sanger sequencing in the extended pedigree.

Results: Radiographs of the female kitten revealed bilateral absence of the radii and bowing of the humeri, while the male kitten showed a dysplastic right radius. Echocardiography suggested the female kitten had restrictive cardiomyopathy with a positive left atrial-to-aortic root ratio (LA:Ao = 1.83 cm), whereas hypertrophic cardiomyopathy was more likely in the sire, showing diastolic dysfunction using tissue Doppler imaging (59.06 cm/s). Twenty-two DNA variants were unique and homozygous in the affected kittens and heterozygous in the parents. Seven variants clustered in one chromosomal region, including two frameshift variants in cardiomyopathy associated 5 (CMYA5) and five variants in junction mediating and regulatory protein, P53 cofactor (JMY ), including a missense and an in-frame deletion.

Conclusions and relevance: The present study suggested an autosomal recessive mode of inheritance with variable expression for RH in the Siamese cat family. Candidate variants for the phenotype were identified, implicating their roles in bone development. These genes should be considered as potentially causal for other cats with RH. Siamese cat breeders should consider genetically testing their cats for these variants to prevent further dissemination of the suspected variants within the breed.

心肌病相关5(CMYA5)被认为是暹罗猫桡侧半肢畸形的遗传危险因素。
目的:本研究旨在确定猫先天性桡骨半肢畸形(RH)的遗传模式和遗传原因。方法:对一个暹罗猫家族(n = 18) ,包括两个患有RH的兄弟姐妹。获得了受影响小猫的放射照片以及受影响小猫和父系的超声心动图。对这两个病例及其父母进行了全基因组测序。基因组数据与99只猫的基因组数据集进行了比较,该数据集由420只额外的家猫组成,具有全基因组和全外显子组测序数据。在患有RH的两个兄弟姐妹中,变异体被认为是纯合子,而在父母中则被认为是杂合子。在扩展谱系中,通过Sanger测序对候选变体进行基因分型。结果:雌性小猫的X线片显示双侧桡骨缺失和肱骨弯曲,而雄性小猫的右桡骨发育异常。超声心动图显示这只雌性小猫患有限制性心肌病,左心房与主动脉根部比率为阳性(LA:Ao = 1.83厘米),而肥厚型心肌病在父系中更可能,使用组织多普勒成像显示舒张功能障碍(59.06厘米/秒)。22种DNA变异在受影响的小猫中是独特的纯合性,在父母中是杂合性。七个变体聚集在一个染色体区域,包括心肌病相关5(CMYA5)中的两个移码变体和连接介导和调节蛋白P53辅因子(JMY ), 包括错义和帧内删除。结论和相关性:本研究提示暹罗猫家族存在RH可变表达的常染色体隐性遗传模式。表型的候选变体已被鉴定,表明它们在骨发育中的作用。这些基因应该被认为是其他患有RH的猫的潜在病因。暹罗猫的饲养者应该考虑对他们的猫进行基因检测,以防止疑似变种在该品种中进一步传播。
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
CiteScore
3.90
自引率
17.60%
发文量
254
审稿时长
8-16 weeks
期刊介绍: JFMS is an international, peer-reviewed journal aimed at both practitioners and researchers with an interest in the clinical veterinary healthcare of domestic cats. The journal is published monthly in two formats: ‘Classic’ editions containing high-quality original papers on all aspects of feline medicine and surgery, including basic research relevant to clinical practice; and dedicated ‘Clinical Practice’ editions primarily containing opinionated review articles providing state-of-the-art information for feline clinicians, along with other relevant articles such as consensus guidelines.
×
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