主要组织相容性复合物-DQA 变异分析:丰富的序列与选择优缺点

Amit Mishra, Rajiv Kumar, Ravi Kumar Sharma, Amar Singh Meena, Kritika Gaur
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摘要

胰岛素依赖型糖尿病是人类的一种自身免疫性疾病,与 MHC-II 类相关,后者会与 MHC-II 类释放的自身肽发生反应。HLA-DQ 等位基因(DQA1 和 DQB1)被发现与人类 1 型糖尿病有关。父母遗传给后代的 DQ 等位基因使后代有患 I 型糖尿病的风险。本研究从绵羊血液中扩增并测序了 DQ 变体(DQA1 和 DQA2),产物大小分别为 826 bp(DQA1)和 865 bp(DQA2)。对序列进行了同源性百分比、系统发育和蛋白质特性的内部鉴定。系统发育分析表明,绵羊体内存在丰富的 DQA 等位基因。拉马钱德兰图分析表明,残基出现在两个 DQ 基因位点的核心区域,分别有 90.8% 和 92.1% 的残基位于 DQA1 和 DQA2 基因位点的优势区域。
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Major Histocompatibility Complex-DQA Variants Analysis: Rich Repertoire with Selection Advantages and Disadvantages
Insulin dependent diabetes mellitus, an autoimmune disorder in human being, is associated with MHC class-II, which reacts with auto peptide released by MHC class-II. HLA-DQ alleles (DQA1 and DQB1) are revealed to be linked with type 1 diabetes in humans. The DQ alleles passed from parents to the offspring predisposes them with risk of type I diabetes. In present study, DQ variants (DQA1 and DQA2) were amplified and sequenced with product size 826 bp (DQA1) and 865 bp (DQA2) from sheep’s blood. Sequences were insilico characterized for percent identity, phylogeny, and protein property. Phylogeny analysis suggests a rich repertoire of DQA alleles in sheep. Ramachandran plot analysis had shown the residues are occurring under the core region of both the DQ loci with 90.8% and 92.1% of residues lie in the favored region in DQA1 and DQA2 loci, respectively.
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