Wilkes D, Shaw J, Anand R, Riley J, Winter P, Wallis J, Driesel A G, Williamson R, Chamberlain S
Department of Biochemistry and Molecular Genetics, St. Mary's Hospital Medical School, London, England.
Genomics. 1991 Jan;9(1):90-5. doi: 10.1016/0888-7543(91)90224-3.
The Friedreich's ataxia locus has been previously assigned to chromosome 9q 13-21.1 by the demonstration of tight linkage to two anonymous DNA markers. MCT112 (Z greater than 80, theta = 0) and DR47 (Z greater than 50, theta = 0). The absence of recombination between these three loci has prevented the resolution of gene/probe order in this region, impeding strategies for gene isolation. We report physical mapping over a 4-Mb genomic interval, linking the markers MCT112 and DR47 on a common 460-kb NotI fragment and identifying 11 CpG islands in the 1.7-Mb interval most likely to contain the Friedreich's ataxia locus. Four of these islands were detected only by analysis of three YAC clones spanning a 700-kb interval including the MCT112/DR47 cluster. Without clear evidence of the precise location of the disease locus from recombination events, each of these regions must be considered as specifying a potential "candidate" sequence for the mutated gene.
通过证明与两个匿名DNA标记紧密连锁,弗里德赖希共济失调基因座先前已被定位到9号染色体的q13 - 21.1区域。这两个标记分别是MCT112(Z大于80,θ = 0)和DR47(Z大于50,θ = 0)。这三个基因座之间不存在重组,使得该区域的基因/探针顺序无法确定,从而阻碍了基因分离策略的实施。我们报告了在一个4兆碱基(Mb)基因组区间内的物理图谱构建,将标记MCT112和DR47连接在一个共同的460千碱基(kb)的NotI片段上,并在最有可能包含弗里德赖希共济失调基因座的1.7兆碱基区间内鉴定出11个CpG岛。其中四个岛仅通过分析三个跨越700千碱基区间(包括MCT112/DR47簇)的酵母人工染色体(YAC)克隆检测到。由于没有从重组事件中获得疾病基因座精确定位的明确证据,这些区域中的每一个都必须被视为指定了突变基因的潜在“候选”序列。