Chan W P, Lee C K, Kwong Y L, Lam C K, Liang R
Department of Medicine, University of Hong Kong, Queen Mary Hospital, Hong Kong.
Blood. 1998 Feb 15;91(4):1135-9.
We have analyzed 83 unrelated Hong Kong Chinese for the presence of genetic variants of factor V gene. Forty-three of them had a history of deep vein thrombosis. The DNA sequence variations of exons 7, 10, and 13, where the codons for Arg306, Arg506, and Arg679 are located, respectively, were studied by denaturing gradient gel electrophoresis. The G1691-->A (Arg 506-->Gln) mutation in exon 10 was not detectable in any of the 83 subjects. However, a high allelic frequency for the G1628-->A (Arg 485-->Lys) substitution was detectable in the same exon. We have also identified a novel DNA sequence mutation (A1090-->G) in exon 7 that resulted in Arg 306-->Gly substitution in 2 thrombotic patients and 1 nonthrombotic subject. Fresh blood samples were available from one of them for analysis of activated protein C resistance and the result was negative. Variation of DNA sequence was not found in exon 13 in any of our 83 subjects. The results of this study showed that, although the Arg 506-->Gln mutation was rarely found in the Hong Kong Chinese population, a different mutation site such as A 1090-->G in exon 7 of the factor V gene (Arg 306) may be of clinical importance.
我们分析了83名无亲缘关系的香港华人,以检测凝血因子V基因的遗传变异情况。其中43人有深静脉血栓形成病史。分别研究了外显子7、10和13的DNA序列变异情况,这三个外显子分别是密码子Arg306、Arg506和Arg679所在的位置,采用变性梯度凝胶电泳进行检测。在83名受试者中均未检测到外显子10中的G1691→A(Arg 506→Gln)突变。然而,在同一外显子中可检测到G1628→A(Arg 485→Lys)替代的高等位基因频率。我们还在2名血栓形成患者和1名非血栓形成受试者中鉴定出一种外显子7中的新型DNA序列突变(A1090→G),该突变导致Arg 306→Gly替代。其中一人有新鲜血液样本,用于分析活化蛋白C抵抗性,结果为阴性。在我们的83名受试者中,外显子13均未发现DNA序列变异。本研究结果表明,尽管在香港华人中很少发现Arg 506→Gln突变,但凝血因子V基因外显子7(Arg 306)中的不同突变位点如A 1090→G可能具有临床意义。