Okada T, Hashimoto R, Numakawa T, Iijima Y, Kosuga A, Tatsumi M, Kamijima K, Kato T, Kunugi H
Department of Mental Disorder Research, National Institute of Neuroscience, National Center of Neurology and Psychiatry, Tokyo, Japan.
Mol Psychiatry. 2006 Jul;11(7):695-703. doi: 10.1038/sj.mp.4001822. Epub 2006 Mar 28.
Previous studies have suggested that genetic variations in the brain-derived neurotrophic factor (BDNF) gene may be associated with several neuropsychiatric diseases including bipolar disorder. The present study examined a microsatellite polymorphism located approximately 1.0 kb upstream of the translation initiation site of the BDNF gene for novel sequence variations, association with bipolar disorder, and effects on transcriptional activity. Detailed sequencing analysis revealed that this polymorphism is not a simple dinucleotide repeat, but it is highly polymorphic with a complex structure containing three types of dinucleotide repeats, insertion/deletion, and nucleotide substitutions that gives rise to a total of 23 novel allelic variants. We obtained evidence supporting the association between this polymorphic region (designated as BDNF-linked complex polymorphic region (BDNF-LCPR)) and bipolar disorder. One of the major alleles ('A1' allele) was significantly more common in patients than in controls (odds ratio 2.8, 95% confidential interval 1.5-5.3, P=0.001). Furthermore, a luciferase reporter gene assay in rat primary cultured neurons suggests that this risk allele (A1) has a lower-transcription activity, compared to the other alleles. Our results suggest that the BDNF-LCPR is a functional variation that confers susceptibility to bipolar disorder and affects transcriptional activity of the BDNF gene.
先前的研究表明,脑源性神经营养因子(BDNF)基因的遗传变异可能与包括双相情感障碍在内的多种神经精神疾病有关。本研究检测了位于BDNF基因翻译起始位点上游约1.0 kb处的一个微卫星多态性,以寻找新的序列变异、与双相情感障碍的关联性以及对转录活性的影响。详细的测序分析表明,这种多态性并非简单的二核苷酸重复,而是高度多态的,具有复杂的结构,包含三种类型的二核苷酸重复、插入/缺失以及核苷酸替换,总共产生了23种新的等位基因变体。我们获得了支持该多态性区域(命名为BDNF连锁复合多态性区域(BDNF-LCPR))与双相情感障碍之间关联的证据。其中一个主要等位基因(“A1”等位基因)在患者中比在对照组中明显更常见(优势比2.8,95%置信区间1.5 - 5.3,P = 0.001)。此外,在大鼠原代培养神经元中进行的荧光素酶报告基因检测表明,与其他等位基因相比,这种风险等位基因(A1)具有较低的转录活性。我们的结果表明,BDNF-LCPR是一种功能性变异,它赋予了双相情感障碍易感性,并影响BDNF基因的转录活性。