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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.

DOI:10.3390/vetsci11120596
PMID:39728936
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11680250/
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。

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本文引用的文献

1
EHBP1L1, an apicobasal polarity regulator, is critical for nuclear polarization during enucleation of erythroblasts.EHBP1L1,一个顶端-基底极性调控蛋白,在红细胞去核过程中对于核的极化起关键作用。
Blood Adv. 2023 Jul 25;7(14):3382-3394. doi: 10.1182/bloodadvances.2022008930.
2
Frameshift Deletion in English Springer Spaniel Dogs with Dyserythropoietic Anemia and Myopathy Syndrome (DAMS) or Neonatal Losses.具有红细胞生成异常性贫血和肌病综合征(DAMS)或新生仔死亡的英国史宾格犬中的移码缺失。
Genes (Basel). 2022 Aug 26;13(9):1533. doi: 10.3390/genes13091533.
3
Lethal variants in humans: lessons learned from a large molecular autopsy cohort.致命性变异在人类中的研究:来自大规模分子尸检队列的经验教训。
Genome Med. 2021 Oct 13;13(1):161. doi: 10.1186/s13073-021-00973-0.
4
EHBP1L1 coordinates Rab8 and Bin1 to regulate apical-directed transport in polarized epithelial cells.EHBP1L1 协调 Rab8 和 Bin1 以调节极化上皮细胞中的顶端定向运输。
J Cell Biol. 2016 Feb 1;212(3):297-306. doi: 10.1083/jcb.201508086.
5
Metabolic myopathy in canine muscle-type phosphofructokinase deficiency.
Muscle Nerve. 1988 Dec;11(12):1260-5. doi: 10.1002/mus.880111210.
6
Dyserythropoiesis, polymyopathy, and cardiac disease in three related English springer spaniels.三只相关的英国激飞猎犬的红细胞生成异常、多肌病和心脏病
J Vet Intern Med. 1991 May-Jun;5(3):151-9. doi: 10.1111/j.1939-1676.1991.tb00942.x.