Townsend Family Laboratories, Department of Psychiatry, Brain Research Center, Graduate Program in Neuroscience, The University of British Columbia, 2255 Wesbrook Mall, Vancouver, BC V6T1Z3, Canada.
J Mol Neurosci. 2010 Sep;42(1):127-33. doi: 10.1007/s12031-010-9381-6. Epub 2010 May 9.
Alzheimer's disease (AD) is the most neurodegenerative disorder leading to dementia. Neuritic plaque formation in brains is a hallmark of AD pathogenesis. Amyloid beta protein (Abeta) is the central component of neuritic plaques. Processing beta-amyloid precursor protein (APP) at the beta-secretase site by the beta-site APP cleaving enzyme 1 (BACE1) is essential for generation of Abeta. Elevation of BACE1 activity and expression has been reported in AD brains. However, no mutation in the BACE1 coding sequence has been identified in AD cases. Human BACE1 expression is tightly regulated at the transcription and translation level. To determine whether there is any single-nucleotide polymorphisms in the BACE1 gene promoter region affecting BACE1 expression in AD pathogenesis, in this study, we screened 2.6 kb of the human BACE1 gene promoter region from late-onset AD patients and found that there was no significant association between single-nucleotide polymorphisms and AD cases.
阿尔茨海默病(AD)是最常见的神经退行性疾病,可导致痴呆。脑中神经突斑块的形成是 AD 发病机制的标志。淀粉样β蛋白(Abeta)是神经突斑块的核心成分。β-淀粉样前体蛋白(APP)在β-分泌酶位点被β-位点 APP 裂解酶 1(BACE1)切割,这对于 Abeta 的产生是必不可少的。在 AD 脑中已经报道了 BACE1 活性和表达的升高。然而,在 AD 病例中并未发现 BACE1 编码序列中的突变。人 BACE1 的表达在转录和翻译水平受到严格调控。为了确定 BACE1 基因启动子区域是否存在任何单核苷酸多态性影响 AD 发病机制中的 BACE1 表达,在这项研究中,我们从迟发性 AD 患者中筛选了 2.6 kb 的人 BACE1 基因启动子区域,发现单核苷酸多态性与 AD 病例之间没有显著关联。