Department of Clinical Chemistry, VU University Medical Center, Amsterdam, The Netherlands.
J Alzheimers Dis. 2012;31(4):793-800. doi: 10.3233/JAD-2012-120472.
STOX1A is a transcription factor which is functionally and structurally similar to the forkhead box protein family. STOX1A has been shown to be associated with pre-eclampsia, a pregnancy associated disease, and to have potential implications in late onset Alzheimer's disease. However, the exact function of STOX1A and its target genes are still largely unknown. Therefore, in this study we performed chromatin immunoprecipitation coupled to shotgun cloning to discover novel STOX1A target genes. Our results show that CNTNAP2, a member of the neurexin family, is directly downregulated by STOX1A. Additionally, we show that CNTNAP2 expression is downregulated in the hippocampus of Alzheimer's disease patients where STOX1A expression has been shown to be upregulated. In conclusion, these results further indicate the potential involvement of STOX1A and its target genes in the etiology of Alzheimer's disease.
STOX1A 是一种转录因子,其功能和结构与叉头框蛋白家族相似。STOX1A 已被证明与子痫前期有关,这是一种与妊娠相关的疾病,并可能与迟发性阿尔茨海默病有关。然而,STOX1A 的确切功能及其靶基因仍在很大程度上未知。因此,在这项研究中,我们进行了染色质免疫沉淀结合鸟枪法克隆,以发现新的 STOX1A 靶基因。我们的结果表明,神经连接蛋白 2(CNTNAP2)是神经连接蛋白家族的成员,其直接受到 STOX1A 的下调。此外,我们还表明,在阿尔茨海默病患者的海马体中,CNTNAP2 的表达下调,而 STOX1A 的表达已被证明上调。总之,这些结果进一步表明 STOX1A 及其靶基因可能参与了阿尔茨海默病的发病机制。