Estivill X, Scambler P J, Wainwright B J, Hawley K, Frederick P, Schwartz M, Baiget M, Kere J, Williamson R, Farrall M
Department of Biochemistry and Molecular Genetics, St. Mary's Hospital Medical School, University of London, England.
Genomics. 1987 Nov;1(3):257-63. doi: 10.1016/0888-7543(87)90052-8.
Four polymorphic markers that map within 80 kb of an HTF island which is genetically very close to the cystic fibrosis locus have been identified. We have analyzed the linkage disequilibrium between each of these markers and the cystic fibrosis mutation in 89 families from four European countries, Denmark, Finland, Spain, and Great Britain. Strong linkage disequilibrium between three polymorphic sites and cystic fibrosis was observed. The markers on the J3.11 (D7S8) side of the HTF island show stronger disequilibrium than those on the met side. Linkage disequilibrium between markers and disease alters the probability that a person of a given haplotype is a carrier in some populations and helps to identify regions of a sequence that are most likely to contain the cystic fibrosis mutation.
已鉴定出四个多态性标记,它们位于一个HTF岛的80 kb范围内,该HTF岛在遗传上与囊性纤维化基因座非常接近。我们分析了来自丹麦、芬兰、西班牙和英国这四个欧洲国家的89个家庭中,这些标记中的每一个与囊性纤维化突变之间的连锁不平衡情况。观察到三个多态性位点与囊性纤维化之间存在强烈的连锁不平衡。HTF岛J3.11(D7S8)一侧的标记显示出比met一侧的标记更强的不平衡。标记与疾病之间的连锁不平衡改变了给定单倍型的人在某些人群中成为携带者的概率,并有助于识别最有可能包含囊性纤维化突变的序列区域。