Migeon B R, Sprenkle J A, Liebaers I, Scott J F, Neufeld E F
Am J Hum Genet. 1977 Sep;29(5):448-54.
Fibroblast cultures derived from the skin of three Hunter heterozygotes have been examined for iduronate sulfatase deficiency primarily by measurement of [35S]-mucopolysaccharide accumulation in the presence and absence of Hunter corrective factor. For each heterozygote, two populations of clones were observed: normal and enzyme deficient, as predicted by the Lyon hypothesis. However, the phenotype of the uncloned cultures was usually normal, presumably because of cross-correction, even after storage in liquid N2. Mixing experiments indicate that the presence of a majority of cells with the Hunter phenotype may be obscured as the result of correction by the minority population of normal cells in the mixture. Variability in the ability to cross-correct was also demonstrated. The unpredictable behavior of uncloned cultures make them unsuitable for diagnosing the Hunter carrier state.
对从三名亨特综合征杂合子皮肤中获取的成纤维细胞培养物进行了检查,主要通过在有和没有亨特校正因子的情况下测量[35S] - 粘多糖积累来检测艾杜糖醛酸硫酸酯酶缺乏症。对于每个杂合子,观察到两个克隆群体:正常和酶缺陷型,正如莱昂假说所预测的那样。然而,未克隆培养物的表型通常是正常的,可能是由于交叉校正,即使在液氮中储存后也是如此。混合实验表明,由于混合物中少数正常细胞的校正作用,具有亨特表型的大多数细胞的存在可能会被掩盖。还证明了交叉校正能力的变异性。未克隆培养物的不可预测行为使其不适用于诊断亨特携带者状态。