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针对 HLA-G 3'非翻译区等位基因和单倍型的 microRNA 的计算机分析。

In silico analysis of microRNAS targeting the HLA-G 3' untranslated region alleles and haplotypes.

机构信息

Division of Clinical Immunology, Department of Medicine, School of Medicine of Ribeirao Preto, University of São Paulo, São Paulo, Brazil.

出版信息

Hum Immunol. 2009 Dec;70(12):1020-5. doi: 10.1016/j.humimm.2009.07.028. Epub 2009 Aug 5.

Abstract

It has been reported that microRNAs (miRNA) may have allele-specific targeting for the 3' untranslated region (3' UTR) of the HLA-G locus. In a previous study, we reported 11 3'UTR haplotypes encompassing the 14-bp insertion/deletion polymorphism and seven SNPs (+3003 T/C, +3010 C/G, +3027 C/A, +3035 C/T, +3142 C/G, +3187 A/G, and +3196 C/G), of which only the +3142 C/G SNP has been reported to influence the binding of miRNAs. Using bioinformatics analyses, we identified putative miRNA-binding sites considering the haplotypes encompassing these eight polymorphic sites, and we ranked the lowest free energies that could potentially lead to an mRNA degradation or translational repression. When a specific haplotype or a particular SNP was associated with a miRNA-binding site, we defined a free energy difference of 4 kcal/mol between alleles to classify them energetically distant. The best results were obtained for the miR-513a-5p, miR-518c*, miR-1262 and miR-92a-1*, miR-92a-2*, miR-661, miR-1224-5p, and miR-433 miRNAs, all influencing one or more of the +3003, +3010, +3027, and +3035 SNPs. The miR-2110, miR-93, miR-508-5p, miR-331-5p, miR-616, miR-513b, and miR-589* miRNAs targeted the 14-bp fragment region, and miR-148a, miR-19a*, miR-152, mir-148b, and miR-218-2 also influenced the +3142 C/G polymorphism. These results suggest that these miRNAs might play a relevant role on the HLA-G expression pattern.

摘要

据报道,微小 RNA(miRNA)可能对 HLA-G 基因座的 3'非翻译区(3'UTR)具有等位基因特异性靶向作用。在之前的研究中,我们报道了 11 个 3'UTR 单倍型,包含 14 个碱基插入/缺失多态性和 7 个 SNP(+3003T/C、+3010C/G、+3027C/A、+3035C/T、+3142C/G、+3187A/G 和 +3196C/G),其中只有+3142C/G SNP 被报道影响 miRNA 的结合。通过生物信息学分析,我们考虑到包含这 8 个多态性位点的单倍型,鉴定了潜在的 miRNA 结合位点,并对可能导致 mRNA 降解或翻译抑制的最低自由能进行了排序。当特定的单倍型或特定的 SNP 与 miRNA 结合位点相关时,我们定义等位基因之间的自由能差异为 4kcal/mol,以将它们归类为能量上的差异。miR-513a-5p、miR-518c*、miR-1262 和 miR-92a-1*、miR-92a-2*、miR-661、miR-1224-5p 和 miR-433 等 miRNA 获得了最佳结果,它们都影响了一个或多个+3003、+3010、+3027 和+3035 SNP。miR-2110、miR-93、miR-508-5p、miR-331-5p、miR-616、miR-513b 和 miR-589miRNA 靶向 14 个碱基片段区域,而 miR-148a、miR-19a、miR-152、mir-148b 和 miR-218-2 也影响了+3142C/G 多态性。这些结果表明,这些 miRNA 可能在 HLA-G 表达模式中发挥重要作用。

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