Hattori Eiji, Nakajima Mizuho, Yamada Kazuo, Iwayama Yoshimi, Toyota Tomoko, Saitou Naruya, Yoshikawa Takeo
Laboratory for Molecular Psychiatry, RIKEN Brain Science Institute, Saitama, Japan.
Eur J Hum Genet. 2009 Jun;17(6):793-801. doi: 10.1038/ejhg.2008.247. Epub 2008 Dec 17.
Associations have been reported between the variable number of tandem repeat (VNTR) polymorphisms in the exon 3 of dopamine D4 receptor gene gene and multiple psychiatric illnesses/traits. We examined the distribution of VNTR alleles of different length in a Japanese cohort and found that, as reported earlier, the size of allele '7R' was much rarer (0.5%) in Japanese than in Caucasian populations (approximately 20%). This presents a challenge to an earlier proposed hypothesis that positive selection favoring the allele 7R has contributed to its high frequency. To further address the issue of selection, we carried out sequencing of the VNTR region not only from human but also from chimpanzee samples, and made inference on the ancestral repeat motif and haplotype by use of a phylogenetic analysis program. The most common 4R variant was considered to be the ancestral haplotype as earlier proposed. However, in a gene tree of VNTR constructed on the basis of this inferred ancestral haplotype, the allele 7R had five descendent haplotypes in relatively long lineage, where genetic drift can have major influence. We also tested this length polymorphism for association with schizophrenia, studying two Japanese sample sets (one with 570 cases and 570 controls, and the other with 124 pedigrees). No evidence of association between the allele 7R and schizophrenia was found in any of the two data sets. Collectively, this study suggests that the VNTR variation does not have an effect large enough to cause either selection or a detectable association with schizophrenia in a study of samples of moderate size.
多巴胺D4受体基因外显子3中可变数目串联重复(VNTR)多态性与多种精神疾病/性状之间的关联已有报道。我们在一个日本队列中检测了不同长度VNTR等位基因的分布,发现正如之前报道的那样,等位基因“7R”在日本人中的比例(0.5%)比高加索人群(约20%)要低得多。这对早期提出的一个假说是一个挑战,该假说认为有利于等位基因7R的正选择导致了其高频率。为了进一步探讨选择问题,我们不仅对人类样本,还对黑猩猩样本的VNTR区域进行了测序,并使用系统发育分析程序推断祖先重复基序和单倍型。正如之前所提出的,最常见的4R变体被认为是祖先单倍型。然而,在基于这种推断的祖先单倍型构建的VNTR基因树中,等位基因7R在相对较长的谱系中有五个衍生单倍型,在这些谱系中遗传漂变可能产生重大影响。我们还在两个日本样本组(一组有570例病例和570例对照,另一组有124个家系)中测试了这种长度多态性与精神分裂症的关联。在这两个数据集中均未发现等位基因7R与精神分裂症之间存在关联的证据。总体而言,这项研究表明,在中等规模样本的研究中,VNTR变异的影响不足以导致选择或与精神分裂症产生可检测到的关联。