Tsui L C, Buchwald M, Barker D, Braman J C, Knowlton R, Schumm J W, Eiberg H, Mohr J, Kennedy D, Plavsic N
Science. 1985 Nov 29;230(4729):1054-7. doi: 10.1126/science.2997931.
A polymorphic DNA marker has been found genetically linked, in a set of 39 human families, to an autosomal recessive gene that causes cystic fibrosis (CF), a disease affecting one in 2000 Caucasian children. The DNA marker (called D0CRI-917) is also linked to the PON locus, which by independent evidence is linked to the CF locus. The best estimates of the genetic distances are 5 centimorgans between the DNA marker and PON and 15 centimorgans between the DNA marker and the CF locus, meaning that the location of the disease gene has been narrowed to about 1 percent of the human genome (about 30 million base pairs). Although the data are consistent with the interpretation that a single locus causes cystic fibrosis, the possibility of genetic heterogeneity remains. The discovery of a linked DNA polymorphism is the first step in molecular analysis of the CF gene and its causative role in the disease.
在39个人类家族中,已发现一种多态性DNA标记与导致囊性纤维化(CF)的常染色体隐性基因存在遗传连锁关系,CF病在2000名高加索儿童中就有1人患病。该DNA标记(称为D0CRI - 917)也与对氧磷酶(PON)基因座连锁,独立证据表明PON基因座与CF基因座相连。遗传距离的最佳估计值为:DNA标记与PON之间为5厘摩,DNA标记与CF基因座之间为15厘摩,这意味着疾病基因的位置已缩小至人类基因组的约1%(约3000万个碱基对)。尽管数据与单一基因座导致囊性纤维化的解释一致,但遗传异质性的可能性仍然存在。连锁DNA多态性的发现是对CF基因及其在疾病中的致病作用进行分子分析的第一步。