Liu J
Institute of Basic Medical Sciences, Beijing.
Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 1990 Apr;12(2):90-5.
beta-Thalassemia is one of the most common single gene disorders in South China, and ten different point mutations and frameshifts have been observed among Chinese. We studied 150 chromosomes of 95 beta-thalassemia patients from Guangxi, Guangdong and Sichuan Provinces using the polymerase chain reaction followed by dot hybridization with specific oligonucleotide probes. The most common mutations were the frameshift at codon 41-42 and the nonsense mutation at codon 17 in Guangxi and Sichuan, and the codon 41-42 frameshift and IVS-II-654 mutation in Guangdong. The A-G mutation at -28 of the promoter was common in Sichuan but not in the other two provinces. Three mutations, -30, IVS-I-1 and IVS-I-5, were not observed. A prenatal diagnosis program using these techniques has been initiated based on these data. Fourteen pregnancies at risk for beta-thalassemia have been diagnosed successfully.
β地中海贫血是中国南方最常见的单基因疾病之一,在中国人群中已观察到10种不同的点突变和移码突变。我们使用聚合酶链反应,随后用特异性寡核苷酸探针进行点杂交,研究了来自广西、广东和四川的95例β地中海贫血患者的150条染色体。最常见的突变在广西和四川是第41-42密码子的移码突变和第17密码子的无义突变,在广东是第41-42密码子移码突变和IVS-II-654突变。启动子-28位点的A-G突变在四川常见,但在其他两个省份未见。未观察到-30、IVS-I-1和IVS-I-5这三种突变。基于这些数据,已启动了一项使用这些技术的产前诊断计划。14例有β地中海贫血风险的妊娠已成功诊断。