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Detection of Three Genetic Polymorphisms in the 5′‐Flanking Region and Intron 1 of Human CYP1A2 in the Japanese Population

机译:日本人群中人CYP1A2 5-侧翼区和内含子1的三种遗传多态性的检测

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摘要

Interindividual variability of the activity of CYP1A2 may be expected to affect cancer susceptibility, since the enzyme is capable of activating several carcinogens. In the present study, we found three new polymorphisms in the 5′‐flanking region (CYP1A2/B) and intron 1 (CYP1A2/C and CYP1A2/D) of CYP1A2 in Japanese by using polymerase chain reaction‐single strand conformation polymorphism. We developed methods to detect these polymorphisms by polymerase chain reaction‐restriction fragment length polymorphism and performed a population study (159 subjects) to estimate the frequencies of the alleles. The frequencies of the CYP1A2/A (adenine), CYP1A2/B (thymine‐deleted), CYP1A2/C (guanine) and CYP1A2/D (adenine) variants were 21.1, 42.0, 8.2 and 61.3%, respectively. The results of family study supported the idea that these CYP1A2 genotypes are inherited with an autosomal codominant transmission.
机译:CYP1A2活性的个体差异可能会影响癌症的易感性,因为该酶能够激活几种致癌物。在本研究中,我们通过聚合酶链反应-单链构象多态性在日本人CYP1A2的5'-侧翼区域(CYP1A2 / B)和内含子1(CYP1A2 / C和CYP1A2 / D)中发现了三个新的多态性。我们开发了通过聚合酶链反应-限制性片段长度多态性检测这些多态性的方法,并进行了一项人群研究(159名受试者)以估计等位基因的频率。 CYP1A2 / A(腺嘌呤),CYP1A2 / B(胸腺嘧啶缺失),CYP1A2 / C(鸟嘌呤)和CYP1A2 / D(腺嘌呤)变异的频率分别为21.1%,42.0、8.2和61.3%。家庭研究的结果支持以下观点:这些CYP1A2基因型以常染色体显性遗传方式遗传。

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