Tóth T, Kristóf T, Ujszászy L, Gerö G, Nagy B, Papp Z
1st Department of Obstetrics and Gynaecology, Semmelweis University Medical School, Budapest, Hungary.
Acta Biol Hung. 1997;48(3):377-83.
The gene responsible for familial adenomatous polyposis (FAP) has recently been mapped, identified and this makes the presymptomatic molecular diagnosis of the disease possible. It can be performed by direct mutation analysis or indirect haplotype analysis. In families where several affected individuals are available the indirect haplotype analysis is the easiest way for performing presymptomatic diagnosis of persons at risk. Among Hungarian families we have performed haplotype analysis using D5S346, a highly polymorphic dinucleotide CA repeat marker located 30-70 kb downstream from APC gene with the combination of restriction endonuclease Rsal site polymorphism. Marker regions were amplified by polymerase chain reaction (PCR) and basen on the above-mentioned polymorphic systems, the haplotype at the APC locus was determined. We believe that haplotype analysis of individuals at risk in large FAP families containing several affected members is a rapid, efficient, and highly valuable method for presymptomatic diagnosis of familial colon polyposis.
导致家族性腺瘤性息肉病(FAP)的基因最近已被定位、识别,这使得对该疾病进行症状前分子诊断成为可能。它可以通过直接突变分析或间接单倍型分析来进行。在有多个患病个体的家庭中,间接单倍型分析是对有患病风险者进行症状前诊断的最简单方法。在匈牙利家庭中,我们使用D5S346进行了单倍型分析,D5S346是一种高度多态性的二核苷酸CA重复标记,位于APC基因下游30 - 70 kb处,并结合了限制性内切酶Rsal位点多态性。通过聚合酶链反应(PCR)扩增标记区域,并基于上述多态性系统确定APC基因座处的单倍型。我们认为,在包含多个患病成员的大型FAP家庭中,对有患病风险的个体进行单倍型分析是一种快速、高效且极具价值的家族性结肠息肉病症状前诊断方法。