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Human NPY promoter variation rs16147:T>C as a moderator of prefrontal NPY gene expression and negative affect.

机译:人NPY启动子变异rs16147:T> C作为前额叶NPY基因表达和负面影响的调节剂。

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摘要

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.
机译:对人和动物的研究表明,NPY在行为应激反应的介导中起着作用。在这里,我们检查了NPY启动子变体rs16147:T> C是否对与行为控制,焦虑和抑郁,前扣带回皮层相关的大脑区域中NPY的表达起作用。在计算机分析中,由rs16147变异产生的DNA结构概况变化表明,在rs16147位点蛋白质结合的等位基因差异。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个人的验尸大脑样本,我们显示rs16147处的等位基因变异有助于调节该区域的NPY mRNA和肽水平。特别地,C等位基因导致基因表达增加。与分子发现相符的是,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,从而复制了rs16147-C作为压力相关精神病理学危险因素的最新发现。 。我们的结果表明rs16147:T> C对于调节NPY基因表达和脑功能的重要性。

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