Foroud Tatiana, Wetherill Leah Flury, Kramer John, Tischfield Jay A, Nurnberger John I, Schuckit Marc A, Xuei Xiaoling, Edenberg Howard J
Indiana University School of Medicine, Indianapolis, Indiana 46202-3002, USA.
Alcohol Clin Exp Res. 2008 Jun;32(6):1023-30. doi: 10.1111/j.1530-0277.2008.00663.x. Epub 2008 Apr 15.
A broad region on chromosome 4q was previously linked to the phenotype of alcohol dependence in the Collaborative Study on the Genetics of Alcoholism sample. A strong positional candidate gene was identified within this region: tachykinin receptor 3 gene (TACR3), which encodes tachykinin receptor 3 (NK3R), the receptor for the tachykinin 3 (neurokinin B) peptide. Pharmacological studies have provided evidence that the administration of NK3R agonists attenuates the intake of alcohol and NK3R can also mediate the acute and chronic behavioral effects of cocaine.
Thirty SNPs were genotyped throughout TACR3. Family based association analysis was performed in 219 European American families to detect an association with alcohol dependence. Subsequent analyses were performed to evaluate the evidence of association with other definitions of alcohol dependence as well as cocaine dependence.
Seven of the 9 SNPs in the 3' region of TACR3 provided significant evidence of association with alcohol dependence (p <or= 0.05). Further analyses suggest that the evidence of association is strongest among those subjects with more severe alcohol dependence (defined by ICD-10) and those with co-morbid cocaine dependence. Haplotype analyses further strengthen the evidence of association in the 3' region of the gene.
These results indicate that sequence variations in TACR3 contribute to the variation in more severe alcohol dependent individuals and those who are also cocaine dependent.
在酒精中毒遗传学合作研究样本中,4号染色体长臂上的一个广泛区域先前被认为与酒精依赖的表型有关。在该区域内鉴定出一个强有力的位置候选基因:速激肽受体3基因(TACR3),它编码速激肽受体3(NK3R),即速激肽3(神经激肽B)肽的受体。药理学研究已提供证据表明,给予NK3R激动剂可减少酒精摄入,且NK3R还可介导可卡因的急性和慢性行为效应。
对整个TACR3基因的30个单核苷酸多态性(SNP)进行基因分型。在219个欧美家庭中进行基于家系的关联分析,以检测与酒精依赖的关联。随后进行分析,以评估与酒精依赖的其他定义以及可卡因依赖的关联证据。
TACR3基因3'区域的9个SNP中的7个提供了与酒精依赖相关的显著证据(p≤0.05)。进一步分析表明,在酒精依赖更严重(根据国际疾病分类第10版定义)以及同时患有可卡因依赖的受试者中,关联证据最强。单倍型分析进一步强化了该基因3'区域的关联证据。
这些结果表明,TACR3基因的序列变异导致了更严重酒精依赖个体以及同时患有可卡因依赖个体的变异。