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BMC Genomics. 2015 Mar 14;16:179. doi: 10.1186/s12864-015-1381-z.

Ageing-associated changes in the human DNA methylome: genomic locations and effects on gene expression.

Author information

1
Department of Microbiology and Immunology, School of Medicine, University of Tampere, Tampere, Finland. saara.marttila@uta.fi.
2
Gerontology Research Center, Tampere, Finland. saara.marttila@uta.fi.
3
Department of Microbiology and Immunology, School of Medicine, University of Tampere, Tampere, Finland. laura.kananen@uta.fi.
4
Gerontology Research Center, Tampere, Finland. laura.kananen@uta.fi.
5
Institute of Biosciences and Medical Technology, University of Tampere, Tampere, Finland. sergei.hayrynen@tut.fi.
6
Department of Microbiology and Immunology, School of Medicine, University of Tampere, Tampere, Finland. juulia.jylhava@uta.fi.
7
Gerontology Research Center, Tampere, Finland. juulia.jylhava@uta.fi.
8
Department of Microbiology and Immunology, School of Medicine, University of Tampere, Tampere, Finland. tapio.l.nevalainen@uta.fi.
9
Gerontology Research Center, Tampere, Finland. tapio.l.nevalainen@uta.fi.
10
Gerontology Research Center, Tampere, Finland. antti.hervonen@uta.fi.
11
School of Health Sciences, University of Tampere, Tampere, Finland. antti.hervonen@uta.fi.
12
Gerontology Research Center, Tampere, Finland. marja.jylha@uta.fi.
13
School of Health Sciences, University of Tampere, Tampere, Finland. marja.jylha@uta.fi.
14
Institute of Biosciences and Medical Technology, University of Tampere, Tampere, Finland. matti.nykter@uta.fi.
15
Department of Microbiology and Immunology, School of Medicine, University of Tampere, Tampere, Finland. mikko.a.hurme@uta.fi.
16
Gerontology Research Center, Tampere, Finland. mikko.a.hurme@uta.fi.
17
Fimlab Laboratories, Tampere, Finland. mikko.a.hurme@uta.fi.

Abstract

BACKGROUND:

Changes in DNA methylation are among the mechanisms contributing to the ageing process. We sought to identify ageing-associated DNA methylation changes at single-CpG-site resolution in blood leukocytes and to ensure that the observed changes were not due to differences in the proportions of leukocytes. The association between DNA methylation changes and gene expression levels was also investigated in the same individuals.

RESULTS:

We identified 8540 high-confidence ageing-associated CpG sites, 46% of which were hypermethylated in nonagenarians. The hypermethylation-associated genes belonged to a common category: they were predicted to be regulated by a common group of transcription factors and were enriched in a related set of GO terms and canonical pathways. Conversely, for the hypomethylation-associated genes only a limited set of GO terms and canonical pathways were identified. Among the 8540 CpG sites associated with ageing, methylation level of 377 sites was also associated with gene expression levels. These genes were enriched in GO terms and canonical pathways associated with immune system functions, particularly phagocytosis.

CONCLUSIONS:

We find that certain ageing-associated immune-system impairments may be mediated via changes in DNA methylation. The results also imply that ageing-associated hypo- and hypermethylation are distinct processes: hypermethylation could be caused by programmed changes, whereas hypomethylation could be the result of environmental and stochastic processes.

PMID:
25888029
PMCID:
PMC4404609
DOI:
10.1186/s12864-015-1381-z
[Indexed for MEDLINE]
Free PMC Article

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