Knight S W, Vulliamy T J, Heiss N S, Matthijs G, Devriendt K, Connor J M, D'Urso M, Poustka A, Mason P J, Dokal I
Department of Haematology, Imperial College School of Medicine, Hammersmith Campus, London, UK.
J Med Genet. 1998 Dec;35(12):993-6. doi: 10.1136/jmg.35.12.993.
Dyskeratosis congenita (DC) is a rare inherited disorder characterised by the early onset of reticulate skin pigmentation, nail dystrophy, and mucosal leucoplakia. In over 80% of cases bone marrow failure develops and this is the main cause of early mortality. The DC1 gene responsible for the X linked form (MIM 305000) of dyskeratosis congenita has been mapped to Xq28. In order to narrow the candidate gene region, genetic linkage analysis was performed in eight X linked pedigrees using a set of markers spanning Xq28. A maximum lod score of 5.31 with no recombinations was achieved with marker DXS1073. Two recombination events were identified; one of these uses X chromosome inactivation pattern analysis to determine carrier status and haplotype analysis to fine map the recombination breakpoint. The fine mapping of these recombination events has enabled the candidate gene region for X linked dyskeratosis congenita to be defined as the 1.4 Mb interval between Xq3274 and DXS1108.
先天性角化不良(DC)是一种罕见的遗传性疾病,其特征为网状皮肤色素沉着、指甲营养不良和黏膜白斑病的早期出现。超过80%的病例会发生骨髓衰竭,这是早期死亡的主要原因。导致X连锁型先天性角化不良(MIM 305000)的DC1基因已被定位到Xq28。为了缩小候选基因区域,利用一组跨越Xq28的标记对8个X连锁家系进行了遗传连锁分析。标记DXS1073获得了最大对数优势分数5.31且无重组。确定了两个重组事件;其中之一利用X染色体失活模式分析来确定携带者状态,并利用单倍型分析来精细定位重组断点。这些重组事件的精细定位使得X连锁先天性角化不良的候选基因区域被定义为Xq3274和DXS1108之间1.4 Mb的区间。