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非洲牛DQA基因座的遗传多样性分析:存在BoLA - DQA3基因座的证据

Analysis of genetic diversity at the DQA loci in African cattle: evidence for a BoLA-DQA3 locus.

作者信息

Ballingall K T, Luyai A, McKeever D J

机构信息

International Livestock Research Institute (ILRI), Box 30709, Nairobi, Kenya.

出版信息

Immunogenetics. 1997;46(3):237-44. doi: 10.1007/s002510050268.

Abstract

We describe the development of a polymerase chain reaction (PCR)-based approach for analysis of genetic diversity at the DQA loci in African Bos indicus and Bos taurus cattle. This approach, equally effective in European and Asian cattle breeds, detects the presence or absence of DQA1 and most duplicated DQA2 genes. Nucleotide and predicted amino acid sequence analysis of the highly polymorphic second exons, in addition to analysis of the locus-specific and relatively non-polymorphic transmembrane, cytoplasmic, and 3-prime untranslated regions, has provided evidence for considerable diversity between each of the duplicated DQA2 genes. Therefore, we propose the designation BoLA-DQA3 for the previously unpublished alleles at the second DQA2 locus. Fourteen distinct PCR restriction fragment length polymorphism (RFLP) patterns, each identifying families of alleles at three DQA loci, can be distinguished. Nucleotide sequence analysis of new PCR-RFLP patterns from 193 Kenyan Boran, Ethiopian Arsi (B. indicus), and Guinean N'Dama (B. taurus) cattle identified 13 DQA1 alleles within eight major allelic families, five DQA2 alleles within a single allelic family, and seven DQA3 alleles within three major allelic families.

摘要

我们描述了一种基于聚合酶链反应(PCR)的方法,用于分析非洲瘤牛和普通牛DQA基因座的遗传多样性。这种方法在欧洲和亚洲牛品种中同样有效,可检测DQA1和大多数重复的DQA2基因的存在与否。除了对位点特异性且相对不具多态性的跨膜、细胞质和3'非翻译区进行分析外,对高度多态的第二外显子进行核苷酸和预测氨基酸序列分析,为每个重复的DQA2基因之间存在相当大的多样性提供了证据。因此,我们提议将第二个DQA2位点上以前未发表的等位基因命名为BoLA-DQA3。可以区分出14种不同的PCR限制性片段长度多态性(RFLP)模式,每种模式可识别三个DQA基因座上的等位基因家族。对来自193头肯尼亚博拉牛、埃塞俄比亚阿尔西牛(瘤牛)和几内亚恩达马牛(普通牛)的新PCR-RFLP模式进行核苷酸序列分析,在八个主要等位基因家族中鉴定出13个DQA1等位基因,在一个等位基因家族中鉴定出5个DQA2等位基因,在三个主要等位基因家族中鉴定出7个DQA3等位基因。

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