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醛脱氢酶缺乏症与酒精敏感性的基因型。无活性的ALDH2(2)等位基因是显性的。

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

作者信息

Crabb D W, Edenberg H J, Bosron W F, Li T K

机构信息

Department of Medicine, Indiana University School of Medicine, Indianapolis 46223.

出版信息

J Clin Invest. 1989 Jan;83(1):314-6. doi: 10.1172/JCI113875.

Abstract

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.

摘要

许多东方人缺乏负责氧化乙醇代谢过程中产生的乙醛的线粒体醛脱氢酶(ALDH2)活性。这些人饮用含酒精饮料时会出现酒精潮红反应。酒精潮红反应是乙醛过度积累的结果,这些不适症状往往会减少酒精摄入量。对这种同四聚体酶的亚基进行了测序,发现无活性酶中的异常是487位的赖氨酸被谷氨酸取代。我们利用聚合酶链反应确定了24名日本人肝脏的基因型。将基因型与表型相关联得出结论,编码异常亚基的等位基因(ALDH2(2))是显性的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/18bf/303676/8b30387d2e99/jcinvest00082-0327-a.jpg

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