Condliffe Daniel, Wong Andrew, Troakes Claire, Proitsi Petroula, Patel Yogen, Chouliaras Leonidas, Fernandes Cathy, Cooper Jonathan, Lovestone Simon, Schalkwyk Leonard, Mill Jonathan, Lunnon Katie
Institute of Psychiatry, King's College London, London, UK.
Department of Psychiatry and Neuropsychology, School for Mental Health and Neuroscience, Maastricht University Medical Centre, Maastricht, the Netherlands.
Neurobiol Aging. 2014 Aug;35(8):1850-4. doi: 10.1016/j.neurobiolaging.2014.02.002. Epub 2014 Feb 6.
Epigenetic processes play a key role in the central nervous system and altered levels of 5-methylcytosine have been associated with a number of neurologic phenotypes, including Alzheimer's disease (AD). Recently, 3 additional cytosine modifications have been identified (5-hydroxymethylcytosine, 5-formylcytosine, and 5-carboxylcytosine), which are thought to be intermediate steps in the demethylation of 5-methylcytosine to unmodified cytosine. Little is known about the frequency of these modifications in the human brain during health or disease. In this study, we used immunofluorescence to confirm the presence of each modification in human brain and investigate their cross-tissue abundance in AD patients and elderly control samples. We identify a significant AD-associated decrease in global 5-hydroxymethylcytosine in entorhinal cortex and cerebellum, and differences in 5-formylcytosine levels between brain regions. Our study further implicates a role for epigenetic alterations in AD.
表观遗传过程在中枢神经系统中起着关键作用,5-甲基胞嘧啶水平的改变与多种神经表型有关,包括阿尔茨海默病(AD)。最近,又鉴定出了另外3种胞嘧啶修饰(5-羟甲基胞嘧啶、5-甲酰基胞嘧啶和5-羧基胞嘧啶),它们被认为是5-甲基胞嘧啶去甲基化为未修饰胞嘧啶过程中的中间步骤。对于这些修饰在健康或疾病状态下的人类大脑中的频率了解甚少。在本研究中,我们使用免疫荧光法来确认人类大脑中每种修饰的存在,并研究它们在AD患者和老年对照样本中的跨组织丰度。我们发现内嗅皮质和小脑中的整体5-羟甲基胞嘧啶与AD相关的显著降低,以及脑区之间5-甲酰基胞嘧啶水平的差异。我们的研究进一步表明表观遗传改变在AD中起作用。