Suppr超能文献

英国可卡犬遗传性肾病相关无义突变的等位基因频率。

Allele frequency of nonsense mutation responsible for hereditary nephropathy in English cocker spaniel dogs.

作者信息

Andrade Larissa Rocha, Caceres Amanda Manara, Trecenti Anelize de Souza, Borges Alexandre Secorun, Oliveira-Filho Jose Paes

机构信息

São Paulo State University (Unesp), School of Veterinary Medicine and Animal Science, Rua Prof. Dr. Walter Mauricio Correa, s/n, 18618-681, Botucatu, Brazil.

出版信息

Vet Anim Sci. 2020 Apr 19;9:100114. doi: 10.1016/j.vas.2020.100114. eCollection 2020 Jun.

Abstract

Hereditary nephropathy is a primary progressive glomerular disease in dogs associated with the c.115A>T mutation in the gene in English cocker spaniel (ECS) dogs. The disease is inherited in an autosomal recessive manner. Hereditary nephropathy has been described in this breed since the late 1940s. To date, there are no data on the prevalence of this disease in Brazil, so the aim of this study was to evaluate the allelic frequency of this mutation in ECS dogs in this country. The DNA samples were purified from blood samples or buccal swabs from 221 ECS dogs. Fragments of the DNA containing the mutation were amplified by PCR and submitted to direct gene sequencing. The allele frequency of the mutation was 0.9%. The presence of the mutation in the ECS dog population in Brazil reveals the importance of performing the genotyping tests in these dogs as a method of diagnosing the disease and identifying heterozygous animals, aiming to reduce clinical cases of disease through mating.

摘要

遗传性肾病是一种主要发生在犬类的进行性肾小球疾病,与英国可卡犬(ECS)基因中的c.115A>T突变有关。该疾病以常染色体隐性方式遗传。自20世纪40年代末以来,该品种犬中就有遗传性肾病的描述。迄今为止,巴西尚无关于该疾病患病率的数据,因此本研究的目的是评估该国ECS犬中该突变的等位基因频率。从221只ECS犬的血液样本或口腔拭子中纯化DNA样本。通过聚合酶链反应(PCR)扩增含有该突变的DNA片段,并进行直接基因测序。该突变的等位基因频率为0.9%。巴西ECS犬种群中该突变的存在揭示了对这些犬进行基因分型检测作为诊断疾病和识别杂合动物的方法的重要性,旨在通过交配减少疾病的临床病例。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验