首页> 美国卫生研究院文献>The Journal of Clinical Investigation >Genotypes for aldehyde dehydrogenase deficiency and alcohol sensitivity. The inactive ALDH2(2) allele is dominant.
【2h】

Genotypes for aldehyde dehydrogenase deficiency and alcohol sensitivity. The inactive ALDH2(2) allele is dominant.

机译:醛脱氢酶缺乏症和酒精敏感性的基因型。非活性ALDH2(2)等位基因占主导。

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Many Orientals lack the mitochondrial aldehyde dehydrogenase (ALDH2) activity responsible for the oxidation of acetaldehyde produced during ethanol metabolism. These individuals suffer the alcohol-flush reaction when they drink alcoholic beverages. The alcohol-flush reaction is the result of excessive acetaldehyde accumulation, and the unpleasant symptoms tend to reduce alcohol consumption. The subunit of this homotetrameric enzyme was sequenced and the abnormality in the inactive enzyme shown to be a substitution of lysine for glutamate at position 487. We have used the polymerase chain reaction to determine the genotypes of 24 livers from Japanese individuals. Correlating genotype with phenotype leads to the conclusion that the allele (ALDH2(2)) encoding the abnormal subunit is dominant.
机译:许多东方人缺乏线粒体醛脱氢酶(ALDH2)活性,该活性导致乙醇代谢过程中产生的乙醛氧化。这些人在喝含酒精的饮料时会发生潮红反应。冲洗酒精的反应是乙醛过度积聚的结果,令人不快的症状往往会减少酒精的消耗。对该同四聚体酶的亚基进行了测序,失活酶的异常表现为在487位的谷氨酸被赖氨酸取代。我们已经使用聚合酶链反应确定了来自日本个体的24种肝脏的基因型。基因型与表型的相关性得出结论,编码异常亚基的等位基因(ALDH2(2))是主要的。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号