Birley Andrew J, James Michael R, Dickson Peter A, Montgomery Grant W, Heath Andrew C, Whitfield John B, Martin Nicholas G
Genetic Epidemiology Unit, Queensland Institute of Medical Research, Brisbane, Australia.
Hum Mol Genet. 2008 Jan 15;17(2):179-89. doi: 10.1093/hmg/ddm295. Epub 2007 Oct 6.
Seven alcohol-metabolizing enzymes are encoded by the human alcohol dehydrogenase (ADH) gene cluster on chromosome 4q22-23. One of these genes, ADH7, is uniquely expressed in the stomach mucosa and can influence metabolism of alcohol before its absorption into the blood. However, the contribution of ADH7 to the overall genetic variation in alcohol oxidation in vivo is unknown. Data on in vivo alcohol metabolism were obtained for 206 Australian twin pairs of Caucasian ancestry, following ingestion of a standard dose (0.75 g kg(-1) body weight) of alcohol. Twenty-five single nucleotide polymorphisms that cover the ADH7 encoding region were genotyped. The patterns of linkage disequilibrium among these SNPs identified a recombinational hotspot within intron 7 of the ADH7 gene. A model for the absorption and elimination of alcohol from the body led to the identification of haplotypes associated with inter-individual variation in the early stages of alcohol metabolism. These are within a 35 kb DNA tract contained in the region 5' of intron 7 in the ADH7 gene. The region accounts for 18% of the linkage for alcohol concentration associated with the ADH region, or approximately 11% of the genetic variance.
七种酒精代谢酶由位于4号染色体q22 - 23区域的人类酒精脱氢酶(ADH)基因簇编码。其中一个基因ADH7,仅在胃黏膜中表达,并且在酒精吸收进入血液之前就能影响其代谢。然而,ADH7对体内酒精氧化总体遗传变异的贡献尚不清楚。在摄入标准剂量(0.75克/千克体重)酒精后,获取了206对具有高加索血统的澳大利亚双胞胎体内酒精代谢的数据。对覆盖ADH7编码区域的25个单核苷酸多态性进行了基因分型。这些单核苷酸多态性之间的连锁不平衡模式在ADH7基因的第7内含子内确定了一个重组热点。一个关于酒精在体内吸收和消除的模型,导致了与酒精代谢早期个体间差异相关的单倍型的识别。这些单倍型位于ADH7基因第7内含子5'端区域内一个35 kb的DNA片段中。该区域占与ADH区域相关的酒精浓度连锁的18%,约占遗传方差的11%。