Suppr超能文献

皮埃蒙特牛品种中关节挛缩和巨舌症的遗传学

Genetics of Arthrogryposis and Macroglossia in Piemontese Cattle Breed.

作者信息

Di Stasio Liliana, Albera Andrea, Pauciullo Alfredo, Cesarani Alberto, Macciotta Nicolò P P, Gaspa Giustino

机构信息

Department of Agricultural, Forest and Food Sciences, University of Torino, Largo Baccini 2, 10095 Grugliasco (TO), Italy.

Associazione Nazionale Allevatori Bovini di Razza Piemontese, strada provinciale Trinita' 31/A, 12061 Carrù (CN), Italy.

出版信息

Animals (Basel). 2020 Sep 24;10(10):1732. doi: 10.3390/ani10101732.

Abstract

Arthrogryposis and macroglossia are congenital pathologies known in several cattle breeds, including Piemontese. As variations in single genes were identified as responsible for arthrogryposis in some breeds, we decided: (i) to test the hypothesis of a similar genetic determinism for arthrogryposis in the Piemontese breed by genotyping affected and healthy animals with a high-density chip and applying genome-wide association study (GWAS), and canonical discriminant analysis (CDA) procedures, and (ii) to investigate with the same approach the genetic background of macroglossia, for which no genetic studies exist so far. The study included 125 animals (63 healthy, 30 with arthrogryposis, and 32 with macroglossia). Differently from what reported for other breeds, the analysis did not evidence a single strong association with the two pathologies. Rather, 23 significant markers on different chromosomes were found (7 associated to arthrogryposis, 11 to macroglossia, and 5 to both pathologies), suggesting a multifactorial genetic mechanism underlying both diseases in the Piemontese breed. In the 100-kb interval surrounding the significant SNPs, 20 and 26 genes were identified for arthrogryposis and macroglossia, respectively, with 12 genes in common to both diseases. For some genes (, , , and ), a possible role in the pathologies can be hypothesized, being involved in processes related to muscular or nervous tissue development. The real involvement of these genes needs to be further investigated and validated.

摘要

关节挛缩和巨舌症是包括皮埃蒙特牛在内的多个牛品种中已知的先天性疾病。由于在某些品种中已确定单基因变异是关节挛缩的病因,我们决定:(i) 通过使用高密度芯片对患病和健康动物进行基因分型,并应用全基因组关联研究 (GWAS) 和典型判别分析 (CDA) 程序,来检验皮埃蒙特牛品种中关节挛缩存在类似遗传决定因素的假设;(ii) 采用相同方法研究巨舌症的遗传背景,目前尚无关于巨舌症的遗传研究。该研究包括125头动物(63头健康,30头有关节挛缩,32头有巨舌症)。与其他品种的报道不同,分析未发现与这两种疾病有单一的强关联。相反,在不同染色体上发现了23个显著标记(7个与关节挛缩相关,11个与巨舌症相关,5个与两种疾病都相关),这表明皮埃蒙特牛品种中这两种疾病都存在多因素遗传机制。在显著单核苷酸多态性 (SNP) 周围的100 kb区间内,分别为关节挛缩和巨舌症鉴定出20个和26个基因,两种疾病共有12个基因。对于某些基因(、、和),可以假设它们在这些疾病中可能发挥作用,因为它们参与了与肌肉或神经组织发育相关的过程。这些基因的实际作用需要进一步研究和验证。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b8c/7598642/89bcc29dbb93/animals-10-01732-g001.jpg

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