Department of Chemistry, University of Kentucky, Lexington, KY, USA.
Sanders-Brown Center on Aging, University of Kentucky, 135 Sanders-Brown Center on Aging, 800 South Limestone S, Lexington, KY, 40536, USA.
J Mol Neurosci. 2017 Oct;63(2):185-197. doi: 10.1007/s12031-017-0969-y. Epub 2017 Sep 2.
Epigenetic modifications to cytosine have been shown to regulate transcription in cancer, embryonic development, and recently neurodegeneration. While cytosine methylation studies are now common in neurodegenerative research, hydroxymethylation studies are rare, particularly genome-wide mapping studies. As an initial study to analyze 5-hydroxymethylcytosine (5-hmC) in the Alzheimer's disease (AD) genome, reduced representation hydroxymethylation profiling (RRHP) was used to analyze more than 2 million sites of possible modification in hippocampal DNA of sporadic AD and normal control subjects. Genes with differentially hydroxymethylated regions were filtered based on previously published microarray data for altered gene expression in hippocampal DNA of AD subjects. Our data show significant pathways for altered levels of 5-hmC in the hippocampus of AD subjects compared to age-matched normal controls involved in signaling, energy metabolism, cell function, gene expression, protein degradation, and cell structure and stabilization. Overall, our data suggest a possible role for the dysregulation of epigenetic modifications to cytosine in late stage AD.
已证实,胞嘧啶的表观遗传修饰可调节癌症、胚胎发育和最近的神经退行性变中的转录。虽然在神经退行性变研究中现在很常见对胞嘧啶甲基化的研究,但羟甲基化研究很少,特别是全基因组作图研究。作为分析阿尔茨海默病(AD)基因组中 5-羟甲基胞嘧啶(5-hmC)的初步研究,使用简化代表性羟甲基化分析(RRHP)分析了散发性 AD 和正常对照受试者海马 DNA 中 200 多万个可能修饰的位点。基于 AD 受试者海马 DNA 中改变的基因表达的先前发表的微阵列数据,根据差异羟甲基化区域筛选基因。与年龄匹配的正常对照相比,我们的数据显示 AD 受试者海马中 5-hmC 水平改变的显著途径涉及信号转导、能量代谢、细胞功能、基因表达、蛋白质降解以及细胞结构和稳定性。总的来说,我们的数据表明,在 AD 的晚期,胞嘧啶的表观遗传修饰可能失调。