| Literature DB >> 26335622 |
Idoia Martin-Guerrero1, Elena de Prado, Maite Ardanaz, Maialen Martin-Arruti, Cristina Garcia-Orad, Isabel Guerra, Irune Ruiz, Iñaki Zabalza, Africa Garcia-Orad.
Abstract
The BCL2 breakage mechanism has been shown to be highly dependent on DNA methylation at the major breakpoint region (MBR) CpG sites. We recently described an increased frequency of BCL2/ JH translocation with aging. It is known that methylation levels change with aging. The present study aimed to determine whether methylation alterations at CpG sites of BCL2 MBR were the cause of increased breakages with aging. We analyzed the methylation levels of three CpG sites on the region by pyrosequencing and studied if methylation levels and/or polymorphisms affecting CpG sites were associated with an increase of translocations. We observed that although the methylation levels of MBR CpG sites were higher in individuals with BCL2/JH translocation, in contrast to our expectations, these levels decreased with the age. Moreover, we show that polymorphisms at those CpG sites leading to absence of methylation seem to be a protective factor for the apparition of translocations.Entities:
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Year: 2015 PMID： 26335622 PMCID： PMC5005837 DOI： 10.1007/s11357-015-9834-5
Source DB: PubMed Journal: Age (Dordr) ISSN： 0161-9152