The DNA Methylome as a biomarker for epigenetic instability and human aging.

Author: Mendelsohn AR, Larrick J.
Affiliation:
Panorama Research Institute, 1230 Bordeaux Dr, Sunnyvale, California, United States, 94089, 408-747-5201, , Regenerative Sciences Institute, , 1230 Bordeaux Dr, Sunnyvale, California, United States, 94089, 650-965-1544; amend@regensci.org.
Conference/Journal: Rejuvenation Res.
Date published: 2013 Jan 22
Other: Word Count: 176



Methylation of DNA is intimately involved in control of mammalian/vertebrate gene expression as part of a complex epigenetic regulatory system. We hypothesize that DNA methylation at CpGs "DNA methylome" evolved to increase stability of the differentiated state in somatic vertebrate cells, especially post-mitotic cells, which may have helped to increase longevity. Therefore, the DNA methylome may play a key role in human aging and be an ideal source of biomarkers aging. A new model that links the methylome to chronological age has been reported by Hannum et al. [1] that accurately predicts age and rate of aging from the DNA methylation state of 71 markers in human blood samples. This model may make possible the development of new anti-aging therapeutics as well as more accurately assess the impact of anti-aging regimens such as caloric restriction and drugs such as rapamycin. Furthermore, the model reveals information loss with increased age consistent with noise-based models of aging. The model may eventually lead to experiments to differentiate the contributions of biomolecular damage and noise/incomplete structural replication during aging.
PMID: 23339475

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