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首页> 外文期刊>Pesquisa Veterinária Brasileira >Prevalence study of SNP c.421G>T in the ADAMTS2 gene responsible for dermatosparaxis in White Dorper sheep in Brazil
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Prevalence study of SNP c.421G>T in the ADAMTS2 gene responsible for dermatosparaxis in White Dorper sheep in Brazil

机译:巴西白杜珀羊皮层疏松的ADAMTS2基因中SNP c.421G> T的患病率研究

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Dermatosparaxis is an autosomal recessive disorder of connective tissue; the disorder is clinically characterized by skin fragility and hyperextensibility. Dermatosparaxis in White Dorper sheep is caused by a single nucleotide polymorphism (SNP) (c.421G>T) in the ADAM metalloproteinase with thrombospondin type 1 motif, 2 ( ADAMTS2 ) gene. The aim of this study was to investigate the prevalence of this SNP in a White Dorper herd in S?£o Paulo state, Brazil. In this study, we collected blood DNA samples from 303 White Dorper sheep and performed polymerase chain reaction to amplify the SNP region. The samples were sequenced to determine the presence of the SNP in the ADAMTS2 gene. The SNP prevalence in the studied population was 15.5%; this finding indicates that more effective control measures should be used to prevent the inheritance of SNP c.421G>T in the ADAMTS2 gene in Brazilian White Dorper herds.
机译:皮肤角膜剥落是结缔组织的常染色体隐性遗传性疾病。该疾病的临床特征是皮肤脆弱和过度伸展。白多珀羊的皮肤角膜剥落是由ADAM金属蛋白酶中具有血小板反应蛋白1型基序2(ADAMTS2)基因的单核苷酸多态性(SNP)(c.421G> T)引起的。这项研究的目的是调查在巴西圣保罗州的白多珀牧群中这种SNP的患病率。在这项研究中,我们收集了303只白色杜泊绵羊的血液DNA样本,并进行了聚合酶链反应以扩增SNP区。对样品进行测序以确定ADAMTS2基因中SNP的存在。在研究人群中SNP患病率为15.5%;这一发现表明,应该使用更有效的控制措施来防止巴西白多珀族ADAMTS2基因中SNP c.421G> T的遗传。

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