Tay G K, Cattley S K, Chorney M J, Hollingsworth P N, Roth M P, Dawkins R L, Witt C S
Centre for Molecular Immunology and Instrumentation, University of Western Australia, Royal Perth Hospital, Perth, Western Australia.
Eur J Immunogenet. 1997 Aug;24(4):275-85. doi: 10.1111/j.1365-2370.1997.tb00021.x.
Genes that predispose to haemochromatosis are though to be located within the several megabases telomeric of HLA-A. Further recombinant mapping has been used previously to map susceptibility genes for diseases such as insulin-dependent diabetes mellitus, myasthenia gravis and cystic fibrosis, and should be useful in relation to haemochromatosis. However, this method requires the recognition of ancestral haplotypes within the susceptibility region. Using a panel of six microsatellite markers from this region (MOG A, MOG B, MOG C, D6S464, D6S306 and D6S105), we show that ancestral haplotypes extend telomeric of HLA-A, at least as far as D6S105. Nine of 14 haplotypes carrying HLA-B7 and HLA-A3 shared the same microsatellite alleles between HLA-A and at least D6S105. Similarly, nine of 10 haplotypes sharing HLA-B8 and HLA-A1 shared the same microsatellite alleles, although a different set to those with HLA-B7 and HLA-A3. Haplotypes representing historical recombination events were also identified. These two findings demonstrate that recombinant mapping may be applicable to the mapping of disease genes in this region.
易患血色素沉着症的基因被认为位于HLA - A端粒的几个兆碱基范围内。先前已使用进一步的重组定位来绘制诸如胰岛素依赖型糖尿病、重症肌无力和囊性纤维化等疾病的易感基因图谱,并且这对于血色素沉着症应该是有用的。然而,这种方法需要识别易感区域内的祖先单倍型。使用来自该区域的一组六个微卫星标记(MOG A、MOG B、MOG C、D6S464、D6S306和D6S105),我们表明祖先单倍型延伸至HLA - A的端粒,至少延伸到D6S105。携带HLA - B7和HLA - A3的14个单倍型中有9个在HLA - A和至少D6S105之间共享相同的微卫星等位基因。同样,共享HLA - B8和HLA - A1的10个单倍型中有9个共享相同的微卫星等位基因,尽管与携带HLA - B7和HLA - A3的单倍型不同。还鉴定出了代表历史重组事件的单倍型。这两个发现表明重组定位可能适用于该区域疾病基因的定位。