Suppr超能文献

利用聚合酶链反应对HLA - A基因座的突变进行分类。

Classification of mutations at the HLA-A locus by use of the polymerase chain reaction.

作者信息

Joseph G, Grist S, Firgaira F, Turner D, Morley A

机构信息

Department of Haematology, Flinders University and Medical Centre, Bedford Park, Australia.

出版信息

Environ Mol Mutagen. 1993;22(3):152-6. doi: 10.1002/em.2850220307.

Abstract

We investigated whether the polymerase chain reaction (PCR) could be used to determine the mechanism of mutation in lymphocyte clones mutated at the HLA-A locus. Three polymorphisms, at Factor XIIIA, D6S109, and intron 3 of the HLA-A gene, were used to study a series of clones previously characterised by Southern blotting (SB) at multiple loci on chromosome 6. For detection of loss of heterozygosity, the results of PCR and SB were concordant in 140 of 141 clones when polymorphism in the Factor XIIIA region was studied and in 144 of 145 clones when polymorphism in the HLA-A gene was studied. For classification of the mechanism of mutation, PCR and SB gave the same result in 88 of 92 clones (96%) when a combination of the HLA-A and Factor XIIIA polymorphisms was used and in 46 of 47 clones (98%) when a combination of the HLA-A and D6S109 polymorphisms was used. The results indicate that PCR provides a simple and reliable method for categorising mutations at the HLA-A locus as arising from mitotic recombination, deletion, or from presumptive minor changes within the gene. Rare events such as gene conversion, nondisjunction, or large deletions extending to the telomere will be misclassified. However, such events are rare for mutations at this locus.

摘要

我们研究了聚合酶链反应(PCR)是否可用于确定在HLA - A位点发生突变的淋巴细胞克隆中的突变机制。利用凝血因子ⅫIA、D6S109和HLA - A基因内含子3的三种多态性,研究了一系列先前通过6号染色体上多个位点的Southern印迹法(SB)进行表征的克隆。为了检测杂合性缺失,当研究凝血因子ⅫIA区域的多态性时,141个克隆中有140个克隆的PCR和SB结果一致;当研究HLA - A基因的多态性时,145个克隆中有144个克隆的PCR和SB结果一致。对于突变机制的分类,当使用HLA - A和凝血因子ⅫIA多态性组合时,92个克隆中有88个克隆(96%)的PCR和SB结果相同;当使用HLA - A和D6S109多态性组合时,47个克隆中有46个克隆(98%)的PCR和SB结果相同。结果表明,PCR为将HLA - A位点的突变分类为有丝分裂重组、缺失或基因内假定的微小变化引起的突变提供了一种简单可靠的方法。诸如基因转换、不分离或延伸至端粒的大片段缺失等罕见事件将被错误分类。然而,此类事件在该位点的突变中很少见。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验