Muntoni S, Wiebusch H, Funke H, Seedorf U, Roskos M, Schulte H, Saku K, Arakawa K, Balestrieri A, Assmann G
Institut für Arterioskleroseforschung, Universität Münster, Germany.
Hum Genet. 1996 Feb;97(2):265-7. doi: 10.1007/BF02265280.
A frequent missense mutation (Thr-6Pro) found in the prepeptide of the lysosomal acid lipase (LAL) gene was analyzed in a cohort of 1003 randomly selected samples from Germany, Japan and Sardinia (Italy). Using the mutagenically separated polymerase chain reaction (MS-PCR), allele frequencies of 0.269, 0.238 and 0.245 were determined in the three populations, respectively. Statistical analysis showed a lack of association with a dyslipidemic phenotype in all three groups. Additionally, in a subgroup of 126 German individuals no association was observed between genotype and LAL activity. We conclude that this mutation appears to be a frequent LAL gene polymorphism causing no impaired function of the enzyme and no measurable dyslipidemia in the general population.
在一组从德国、日本和撒丁岛(意大利)随机选取的1003个样本中,对溶酶体酸性脂肪酶(LAL)基因前肽中发现的一种常见错义突变(苏氨酸-6至脯氨酸)进行了分析。使用诱变分离聚合酶链反应(MS-PCR),在这三个人群中分别测定的等位基因频率为0.269、0.238和0.245。统计分析表明,在所有三组中均缺乏与血脂异常表型的关联。此外,在126名德国个体的亚组中,未观察到基因型与LAL活性之间的关联。我们得出结论,这种突变似乎是一种常见的LAL基因多态性,在普通人群中不会导致酶功能受损和可测量的血脂异常。