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An insertion/deletion polymorphism in the angiotensin I-converting enzyme gene accounting for half the variance of serum enzyme levels.

机译:血管紧张素I转换酶基因中的插入/缺失多态性占血清酶水平变化的一半。

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摘要

A polymorphism consisting of the presence or absence of a 250-bp DNA fragment was detected within the angiotensin I-converting enzyme gene (ACE) using the endothelial ACE cDNA probe. This polymorphism was used as a marker genotype in a study involving 80 healthy subjects, whose serum ACE levels were concomitantly measured. Allele frequencies were 0.6 for the shorter allele and 0.4 for the longer allele. A marked difference in serum ACE levels was observed between subjects in each of the three ACE genotype classes. Serum immunoreactive ACE concentrations were, respectively, 299.3 +/- 49, 392.6 +/- 66.8, and 494.1 +/- 88.3 micrograms/liter, for homozygotes with the longer allele (n = 14), and heterozygotes (n = 37) and homozygotes (n = 29) with the shorter allele. The insertion/deletion polymorphism accounted for 47% of the total phenotypic variance of serum ACE, showing that the ACE gene locus is the major locus that determines serum ACE concentration. Concomitant determination of the ACE genotype will improve discrimination between normal and abnormal serum ACE values by allowing comparison with a more appropriate reference interval.
机译:使用内皮ACE cDNA探针在血管紧张素I转换酶基因(ACE)中检测到包含250 bp DNA片段存在或不存在的多态性。在涉及80位健康受试者的研究中,该多态性被用作标记基因型,同时测量了其血清ACE水平。等位基因频率对于较短的等位基因是0.6,对于较长的等位基因是0.4。在三种ACE基因型类别的受试者之间观察到血清ACE水平存在显着差异。等位基因较长的纯合子(n = 14)和杂合子(n = 37)的血清免疫反应性ACE浓度分别为299.3 +/- 49、392.6 +/- 66.8和494.1 +/- 88.3微克/升。等位基因较短的纯合子(n = 29)。插入/缺失多态性占血清ACE总表型变异的47%,表明ACE基因位点是决定血清ACE浓度的主要位点。通过允许与更合适的参考间隔进行比较,同时确定ACE基因型可提高正常和异常血清ACE值之间的区别。

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