Sun Hsiao Fang Sunny, Chang Yuh Terng, Fann Cathy Shen-Jang, Chang Ching Jui, Chen Yi Hsin, Hsu Yun Pung, Yu Wu Yang, Cheng Andrew Tai-Ann
Institute of Molecular Medicine, National Cheng Kung University Medical College, Tainan, Taiwan.
Biol Psychiatry. 2002 Jun 1;51(11):896-901. doi: 10.1016/s0006-3223(01)01366-x.
Abnormal serotonergic pathways are implicated in numerous neuropsychiatric disorders, such as depression, anxiety, migraine, substance abuse, and alcoholism. The human serotonin receptor 1B, encoded by the HTR1B gene, is a presynaptic serotonin autoreceptor that plays a role in regulating serotonin synthesis and release. Because the linkage of antisocial alcoholism to the HTR1B gene was recently reported in two populations, it was of interest to identify genetic variants at the HTR1B locus and study their association with alcoholism in the Taiwanese Han population.
We sequenced DNA from Taiwanese Han to screen for genetic variation in the coding, promoter, and partial 3' untranslated regions of the HTR1B locus of 158 alcohol-dependent cases with withdrawal symptoms and 149 control subjects, who either never drank or drank only occasionally and in low quantities.
Seven variants were identified. Positive associations were found between variant A-161T and alcohol dependence at both the allelic and genotypic level. In addition, an expression study showed that the A-161T variant affected reporter gene activity.
Our results support an association between HTR1B and alcohol dependence. The HTR1B A-161T polymorphism may be valuable both as a functional and as an anonymous genetic marker for HTR1B.
异常的血清素能通路与多种神经精神疾病有关,如抑郁症、焦虑症、偏头痛、药物滥用和酒精中毒。由HTR1B基因编码的人类血清素受体1B是一种突触前血清素自身受体,在调节血清素的合成和释放中发挥作用。由于最近在两个人群中报道了反社会酒精中毒与HTR1B基因的连锁关系,因此有必要在台湾汉族人群中鉴定HTR1B基因座的遗传变异,并研究它们与酒精中毒的关联。
我们对台湾汉族人群的DNA进行测序,以筛选158例有戒断症状的酒精依赖病例和149名对照受试者(从不饮酒或仅偶尔少量饮酒)的HTR1B基因座编码区、启动子区和部分3'非翻译区的遗传变异。
共鉴定出7个变异。在等位基因和基因型水平上,变异A-161T与酒精依赖之间均存在正相关。此外,一项表达研究表明,A-161T变异影响报告基因活性。
我们的结果支持HTR1B与酒精依赖之间存在关联。HTR1B基因的A-161T多态性作为HTR1B的功能性和匿名性遗传标记可能具有重要价值。