Suppr超能文献

英国激飞猎犬红细胞生成异常性贫血和肌病综合征的欧洲基因分型调查

European Genotyping Survey of Dyserythropoietic Anemia and Myopathy Syndrome in English Springer Spaniels.

作者信息

Østergård Jensen Sarah, Kehl Alexandra, Giger Urs

机构信息

AniCura Small Animal Referral Hospital Bagarmossen, Ljusnevägen 17, Bagarmossen, SE-12848 Stockholm, Sweden.

LABOKLIN GmbH & Co. KG, Steubenstr. 4, DE-97688 Bad Kissingen, Germany.

出版信息

Vet Sci. 2024 Nov 26;11(12):596. doi: 10.3390/vetsci11120596.

Abstract

Dyserythropoietic anemia and myopathy syndrome (DAMS) with neonatal losses was recently characterized as an autosomal recessive disorder caused by an frameshift variant in English Springer Spaniels (ESSPs). The frequency and dissemination of the mutation remained unknown. The EHBP1L1 protein is essential for muscle function, and the Rab8/10-EHBP1L1-Bin1-dynamin axis participates in nuclear polarization during the enucleation of erythroblasts. Lack of EHBP1L1 function decreases enucleation, leading to increased numbers of nucleated erythrocytes, which are characteristic of DAMS. A genotyping survey for the variant was conducted based upon submitted samples of ESSPs from Europe. DNA was extracted, and a real-time PCR assay, with allele-specific TaqMan probes for wild-type and frameshift deletion, was applied. Between September 2022 and August 2024, 803 samples were received from 18 European countries. The mutant allele frequency was 9.7%, including 4 homozygous dogs and 148 heterozygotes. The mutant allele was found in 13 countries. A total of 6 homozygous and 73 heterozygous ESSPs reported on an open database could be tracked to an original common ancestor. Although the survey is biased, it indicates that the mutant variant is disseminated in the breed and across Europe. The genotyping of ESSPs is recommended to diagnose DAMS and guide breeders.

摘要

伴有新生儿死亡的异常红细胞生成性贫血和肌病综合征(DAMS)最近被确定为一种常染色体隐性疾病,由英国激飞猎犬(ESSPs)中的一个移码变异引起。该突变的频率和传播情况尚不清楚。EHBP1L1蛋白对肌肉功能至关重要,并且Rab8/10-EHBP1L1-Bin1-发动蛋白轴在成红细胞去核过程中参与细胞核极化。缺乏EHBP1L1功能会减少去核,导致有核红细胞数量增加,这是DAMS的特征。基于来自欧洲的ESSPs提交样本,对该变异进行了基因分型调查。提取DNA,并应用一种实时PCR检测方法,使用针对野生型和移码缺失的等位基因特异性TaqMan探针。在2022年9月至2024年8月期间,从18个欧洲国家收到了803个样本。突变等位基因频率为9.7%,包括4只纯合犬和148只杂合子。在13个国家发现了突变等位基因。在一个开放数据库中报告的总共6只纯合和73只杂合ESSPs可以追溯到一个原始共同祖先。尽管该调查存在偏差,但它表明突变变异在该品种中以及整个欧洲都有传播。建议对ESSPs进行基因分型以诊断DAMS并指导育种者。

相似文献

5
Haemolytic anaemia and exercise intolerance due to phosphofructokinase deficiency in related springer spaniels.
J Small Anim Pract. 2001 Jun;42(6):298-300. doi: 10.1111/j.1748-5827.2001.tb02043.x.

本文引用的文献

5
Metabolic myopathy in canine muscle-type phosphofructokinase deficiency.
Muscle Nerve. 1988 Dec;11(12):1260-5. doi: 10.1002/mus.880111210.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验