Lemonde Sylvie, Turecki Gustavo, Bakish David, Du Lisheng, Hrdina Pavel D, Bown Christopher D, Sequeira Adolfo, Kushwaha Neena, Morris Stephen J, Basak Ajoy, Ou Xiao-Ming, Albert Paul R
Ottawa Health Research Institute (Neuroscience), University of Ottawa, Department of Medicine, Ottawa, Canada, K1H 8M5.
J Neurosci. 2003 Sep 24;23(25):8788-99. doi: 10.1523/JNEUROSCI.23-25-08788.2003.
Inhibition of serotonergic raphe neurons is mediated by somatodendritic 5-HT1A autoreceptors, which may be increased in depressed patients. We report an association of the C(-1019)G 5-HT1A promoter polymorphism with major depression and suicide in separate cohorts. In depressed patients, the homozygous G(-1019) allele was enriched twofold versus controls (p = 0.0017 and 0.0006 for G/G genotype and G allele distribution, respectively), and in completed suicide cases the G(-1019) allele was enriched fourfold (p = 0.002 and 0.00008 for G/G genotype and G allele distribution, respectively). The C(-1019) allele was part of a 26 bp imperfect palindrome that bound transcription factors nuclear NUDR [nuclear deformed epidermal autoregulatory factor (DEAF-1)]/suppressin and Hairy/Enhancer-of-split-5 (Drosophila) (Hes5) to repress 5-HT1A or heterologous promoters, whereas the G(-1019) allele abolished repression by NUDR, but only partially impaired Hes5-mediated repression. Recombinant NUDR bound specifically to the 26 bp palindrome, and endogenous NUDR was present in the major protein-DNA complex from raphe nuclear extracts. Stable expression of NUDR in raphe cells reduced levels of endogenous 5-HT1A protein and binding. NUDR protein was colocalized with 5-HT1A receptors in serotonergic raphe cells, hippocampal and cortical neurons, and adult brain regions including raphe nuclei, indicating a role in regulating 5-HT1A autoreceptor expression. Our data indicate that NUDR is a repressor of the 5-HT1A receptor in raphe cells the function of which is abrogated by a promoter polymorphism. We suggest a novel transcriptional model in which the G(-1019) allele derepresses 5-HT1A autoreceptor expression to reduce serotonergic neurotransmission, predisposing to depression and suicide.
血清素能中缝核神经元的抑制作用由树突体5-HT1A自身受体介导,而抑郁症患者的该受体数量可能会增加。我们报告了C(-1019)G 5-HT1A启动子多态性与不同队列中的重度抑郁症和自杀之间的关联。在抑郁症患者中,纯合G(-1019)等位基因相对于对照组增加了两倍(G/G基因型和G等位基因分布的p值分别为0.0017和0.0006),而在自杀死亡病例中,G(-1019)等位基因增加了四倍(G/G基因型和G等位基因分布的p值分别为0.002和0.00008)。C(-1019)等位基因是一个26 bp的不完全回文序列的一部分,该序列可结合转录因子核NUDR [核变形表皮自调节因子(DEAF-1)]/抑制素以及毛状/分裂增强子-5(果蝇)(Hes5),从而抑制5-HT1A或异源启动子,而G(-1019)等位基因则消除了NUDR的抑制作用,但仅部分削弱了Hes5介导的抑制作用。重组NUDR特异性结合26 bp回文序列,并且内源性NUDR存在于中缝核提取物的主要蛋白质-DNA复合物中。NUDR在中缝核细胞中的稳定表达降低了内源性5-HT1A蛋白的水平和结合能力。NUDR蛋白与血清素能中缝核细胞、海马和皮质神经元以及包括中缝核在内的成人大脑区域中的5-HT1A受体共定位,表明其在调节5-HT1A自身受体表达中发挥作用。我们的数据表明,NUDR是中缝核细胞中5-HT1A受体的一种抑制因子,其功能因启动子多态性而被废除。我们提出了一种新的转录模型,其中G(-1019)等位基因解除对5-HT1A自身受体表达的抑制,从而减少血清素能神经传递,易引发抑郁症和自杀。