Lesch K P, Meyer J, Glatz K, Flügge G, Hinney A, Hebebrand J, Klauck S M, Poustka A, Poustka F, Bengel D, Mössner R, Riederer P, Heils A
Department of Psychiatry, University of Würzburg, Federal Republic of Germany.
J Neural Transm (Vienna). 1997;104(11-12):1259-66. doi: 10.1007/BF01294726.
By conferring allele-specific transcriptional activity on the 5-HT transporter gene promoter in humans, the 5-HT transporter gene-linked polymorphic region (5-HTTLPR) influences a constellation of personality traits related to anxiety and increases the risk for neurodevelopmental, neurodegenerative, and psychiatric disorders. Here we have analyzed the presence and variability of the 5-HTTLPR in several species of primates including humans, and other mammals. PCR, Southern blot, and sequence analyses of the 5-HT transporter gene's 5'-flanking region in different mammalian species confirmed the presence of the 5-HTTLPR in platyrrhini and catarrhini (hominoids, cercopithecoids) but not in prosimian primates and other mammals. Since the 5-HTTLPR is unique to humans and simian primates, a progenitor 5-HTTLPR sequence may have been introduced into the genome some 40 Mio, years ago. In humans the majority of alleles are composed of either 14 or 16 repeat elements, while alleles with 18 or 20 repeat elements are rare. In contrast, great apes including orang-utan, gorilla, and chimpanzee display a high prevalence of alleles with 18 and 20 repeat elements. In hominoids all alleles originate from variation at a single locus (polymorphic locus 1). In the 5-HTTLPR of rhesus monkeys (rh5-HTTLPR) we found an alternative locus for length variation (polymorphic locus 2) generated by a 21 bp insertion/deletion event. The existence of a distinct biallelic variation of the 5-HTTLPR in rhesus monkeys but similar allele and genotype frequencies in this species and humans supports the notion that there may be a relationship between functional 5-HT transporter expression, anxiety-related traits, and the complexity of socialization in human and non-human primate populations.
5-羟色胺转运体基因连锁多态性区域(5-HTTLPR)通过赋予人类5-羟色胺转运体基因启动子等位基因特异性转录活性,影响一系列与焦虑相关的人格特质,并增加神经发育、神经退行性和精神疾病的风险。在此,我们分析了包括人类在内的几种灵长类动物以及其他哺乳动物中5-HTTLPR的存在情况和变异性。对不同哺乳动物物种5-羟色胺转运体基因5'侧翼区域进行聚合酶链反应(PCR)、Southern印迹和序列分析,证实阔鼻猴类和狭鼻猴类(类人猿、猕猴)存在5-HTTLPR,而原猴亚目灵长类动物和其他哺乳动物中则不存在。由于5-HTTLPR是人类和猿猴灵长类动物所特有的,其祖先序列可能在约4000万年前被引入基因组。在人类中,大多数等位基因由14或16个重复元件组成,而含18或20个重复元件的等位基因则很罕见。相比之下,包括猩猩、大猩猩和黑猩猩在内的大型猿类中,含18和20个重复元件的等位基因普遍存在。在类人猿中,所有等位基因都源自单个位点(多态性位点1)的变异。在恒河猴的5-HTTLPR(rh5-HTTLPR)中,我们发现了一个由21 bp插入/缺失事件产生的长度变异的替代位点(多态性位点2)。恒河猴中5-HTTLPR存在明显的双等位基因变异,但该物种与人类的等位基因和基因型频率相似,这支持了功能性5-羟色胺转运体表达、焦虑相关特质以及人类和非人类灵长类种群社交复杂性之间可能存在关联的观点。