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Human leukocyte telomere length is associated with DNA methylation levels in multiple subtelomeric and imprinted loci.
- Source :
-
Scientific reports [Sci Rep] 2014 May 14; Vol. 4, pp. 4954. Date of Electronic Publication: 2014 May 14. - Publication Year :
- 2014
-
Abstract
- In humans, leukocyte telomere length (LTL) is positively correlated with lifespan, and shorter LTL is associated with increased risk of age-related disease. In this study we tested for association between telomere length and methylated cytosine levels. Measurements of mean telomere length and DNA methylation at >450,000 CpG sites were obtained for both blood (N = 24) and EBV-transformed cell-line (N = 36) DNA samples from men aged 44-45 years. We identified 65 gene promoters enriched for CpG sites at which methylation levels are associated with leukocyte telomere length, and 36 gene promoters enriched for CpG sites at which methylation levels are associated with telomere length in DNA from EBV-transformed cell-lines. We observed significant enrichment of positively associated methylated CpG sites in subtelomeric loci (within 4 Mb of the telomere) (P < 0.01), and also at loci in imprinted regions (P < 0.001). Our results pave the way for further investigations to help elucidate the relationships between telomere length, DNA methylation and gene expression in health and disease.
- Subjects :
- Adolescent
Adult
Binding Sites
Child
Child, Preschool
Cluster Analysis
CpG Islands
DNA-Binding Proteins metabolism
Humans
Infant
Infant, Newborn
Male
Middle Aged
Promoter Regions, Genetic
Protein Binding
Repressor Proteins
Signal Transduction
Transcription Factors metabolism
Transcription Initiation Site
Young Adult
DNA Methylation
Genomic Imprinting
Leukocytes metabolism
Telomere genetics
Telomere metabolism
Telomere Homeostasis
Subjects
Details
- Language :
- English
- ISSN :
- 2045-2322
- Volume :
- 4
- Database :
- MEDLINE
- Journal :
- Scientific reports
- Publication Type :
- Academic Journal
- Accession number :
- 24828261
- Full Text :
- https://doi.org/10.1038/srep04954