HLA I 类基因非翻译启动子区域的序列和系统发育分析。

Veron Ramsuran, Pedro G Hernández-Sanchez, Colm O'hUigin, Gaurav Sharma, Niamh Spence, Danillo G Augusto, Xiaojiang Gao, Christian A García-Sepúlveda, Gurvinder Kaur, Narinder K Mehra, Mary Carrington
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摘要

位于 MHC 内的多态性与许多疾病结果有关,其机制在大多数情况下尚未完全明了。位于 HLA 基因非翻译区的变异参与了等位基因的特异性表达,因此可能是其中一些疾病关联的基础。我们测定了来自 57 个主要 HLA I 类基因系的 68 个等位基因的转录起始位点上游近 2 kb 的序列。该启动子片段的核苷酸多样性与编码区的核苷酸多样性大致相同,HLA-B 的多样性最高(1.9%),其次是 HLA-A(1.8%),HLA-C 的多样性最低(0.9%)。尽管HLA-B的多样性较高,但在178名欧洲裔美国人中测定的HLA-B mRNA表达水平并没有等位基因或血统特异性的变化,这与之前报道的HLA-A或HLA-C的不同表达水平不同。大多数 HLA-A 和 -C 基因座表达模式的相似性大致反映了系统发生树中启动子序列的接近性。虽然启动子序列的差异可能会影响启动子的活性,但我们观察到,启动子区域的成对核苷酸差异所代表的系统发生结构与经典 I 类基因位点 mRNA 表达水平的估计差异之间没有明显的联系。此外,没有一对 I 类基因座显示出协调的表达水平,这表明在非刺激条件下,不同基因座的表达水平由不同的机制决定。这些数据为更深入地分析经典 HLA I 类基因座启动子区域变异的功能性后果奠定了基础。
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Sequence and Phylogenetic Analysis of the Untranslated Promoter Regions for HLA Class I Genes.

Polymorphisms located within the MHC have been linked to many disease outcomes by mechanisms not yet fully understood in most cases. Variants located within untranslated regions of HLA genes are involved in allele-specific expression and may therefore underlie some of these disease associations. We determined sequences extending nearly 2 kb upstream of the transcription start site for 68 alleles from 57 major lineages of classical HLA class I genes. The nucleotide diversity within this promoter segment roughly follows that seen within the coding regions, with HLA-B showing the highest (∼1.9%), followed by HLA-A (∼1.8%), and HLA-C showing the lowest diversity (∼0.9%). Despite its greater diversity, HLA-B mRNA expression levels determined in 178 European Americans do not vary in an allele- or lineage-specific manner, unlike the differential expression levels of HLA-A or HLA-C reported previously. Close proximity of promoter sequences in phylogenetic trees is roughly reflected by similarity of expression pattern for most HLA-A and -C loci. Although promoter sequence divergence might impact promoter activity, we observed no clear link between the phylogenetic structures as represented by pairwise nucleotide differences in the promoter regions with estimated differences in mRNA expression levels for the classical class I loci. Further, no pair of class I loci showed coordinated expression levels, suggesting that distinct mechanisms across loci determine their expression level under nonstimulated conditions. These data serve as a foundation for more in-depth analysis of the functional consequences of promoter region variation within the classical HLA class I loci.

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