Can the rDNA methylation pattern be used as a marker for Alzheimer's disease?

• Published in: Alzheimer's & dementia Vol. 4; no. 6; pp. 438 - 442
• Main Authors: Sperança, Márcia Aparecida, Batista, Lisandra Mesquita, da Silva Lourenço, Ricardo, Tavares, Wagner Malagó, Bertolucci, Paulo Henrique Ferreira, de Oliveira Santos Rigolin, Valdeci, Payão, Spencer Luiz Marques, de Arruda Cardoso Smith, Marília
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 01-11-2008
• Subjects: Adult; Aged; Aged, 80 and over; Ageing; Aging - genetics; Alzheimer Disease - diagnosis; Alzheimer Disease - genetics; Alzheimer's disease; Analysis of the human rDNA methylation pattern in ageing and Alzheimer's disease; Blotting, Southern; Case-Control Studies; DNA Methylation; DNA, Ribosomal - genetics; Female; Gene Expression; Human rDNA; Humans; Male; Middle Aged; Neurology; Promoter Regions, Genetic; RNA, Ribosomal, 18S - genetics; RNA, Ribosomal, 28S - genetics; rRNA expression; Alzheimer's disease; rRNA expression; Analysis of the human rDNA methylation pattern in ageing and Alzheimer's disease; Ageing; Human rDNA
• ISSN: 1552-5260; 1552-5279
• DOI: 10.1016/j.jalz.2008.03.010

Abstract Background Differential methylation activity of the human rDNA in Alzheimer's disease (AD) patients has been demonstrated by classic cytogenetic tools, indicating a decrease in rRNA gene expression. Methylation of CpGs is an important epigenetic mechanism involved in gene expression repression of tandem repeating genes during ageing. Thus, rDNA specific methylation pattern could be involved in AD and be used as a marker of the disease or of its progression. Methods The methylation pattern of three rDNA regions, including the promoter, 18S, and 28S, was investigated with the use of restriction endonucleases sensitive to methylation and Southern blotting from DNA extracted from total peripheral blood cells of 28 AD patients and 28 elderly and young controls. Results We did not find a significant divergence in the methylation pattern of the studied regions and in the relative amount of rDNA methylated copies among the individuals' groups. Conclusions No differential methylation pattern of rDNA genes was observed in total peripheral blood cells in aged and AD subjects by the methodology used.