Laboratory of Clinical and Translational Studies, NIAAA, National Institutes of Health, Bethesda, USA.
Hum Mutat. 2010 Aug;31(8):E1594-608. doi: 10.1002/humu.21299.
Studies in humans and animals suggest a role for NPY in the mediation of behavioral stress responses. Here, we examined whether the NPY promoter variant rs16147:T>C is functional for expression of NPY in a brain region relevant for behavioral control, anxiety and depression, the anterior cingulate cortex. In silico analysis of DNA structural profile changes produced by rs16147 variation suggests allelic differences in protein binding at the rs16147 site. This was confirmed by electrophoretic mobility shift assay, demonstrating that the rs16147 C-allele has strongly reduced affinity for a yet unknown factor compared to the T-allele. Analyzing 107 human post-mortem brain samples we show that allelic variation at rs16147 contributes to regulation of NPY mRNA and peptide levels in this region. Specifically, the C-allele leads to increased gene expression. In agreement with the molecular findings, rs16147:T>C is associated with anxiety and depressive symptoms in 314 young adults via a gene x environment interaction with early childhood adversity, replicating the recent finding of rs16147-C as a risk factor for stress related psychopathology. Our results show the importance of rs16147:T>C for regulation of NPY gene expression and brain function.
在人类和动物研究中,NPY 被认为在介导行为应激反应中发挥作用。在这里,我们研究了 NPY 启动子变异 rs16147:T>C 是否对与行为控制、焦虑和抑郁相关的脑区——前扣带回皮层中的 NPY 表达具有功能。对 rs16147 变异产生的 DNA 结构特征变化的计算机分析表明,rs16147 位点的蛋白质结合存在等位基因差异。电泳迁移率变动分析证实了这一点,表明与 T 等位基因相比,rs16147 C 等位基因对未知因子的亲和力大大降低。分析 107 个人类死后大脑样本,我们表明 rs16147 等位基因变异有助于该区域 NPY mRNA 和肽水平的调节。具体来说,C 等位基因导致基因表达增加。与分子发现一致,rs16147:T>C 通过与儿童早期逆境的基因 x 环境相互作用,与 314 名年轻人的焦虑和抑郁症状相关,复制了 rs16147-C 作为与应激相关的精神病理学风险因素的最近发现。我们的研究结果表明 rs16147:T>C 对 NPY 基因表达和大脑功能调节的重要性。