Genome-wide DNA methylation analysis in blood cells from patients with Werner syndrome

T. Guastafierro, M. G. Bacalini, A. Marcoccia, D. Gentilini, S. Pisoni, A. M. Di Blasio, A. Corsi, C. Franceschi, D. Raimondo, A. Spanò, P. Garagnani, F. Bondanini

Research output: Contribution to journalArticle

13 Citations (Scopus)

Abstract

Background: Werner syndrome is a progeroid disorder characterized by premature age-related phenotypes. Although it is well established that autosomal recessive mutations in the WRN gene is responsible for Werner syndrome, the molecular alterations that lead to disease phenotype remain still unidentified. Results: To address whether epigenetic changes can be associated with Werner syndrome phenotype, we analysed genome-wide DNA methylation profile using the Infinium MethylationEPIC BeadChip in the whole blood from three patients affected by Werner syndrome compared with three age- and sex-matched healthy controls. Hypermethylated probes were enriched in glycosphingolipid biosynthesis, FoxO signalling and insulin signalling pathways, while hypomethylated probes were enriched in PI3K-Akt signalling and focal adhesion pathways. Twenty-two out of 47 of the differentially methylated genes belonging to the enriched pathways resulted differentially expressed in a publicly available dataset on Werner syndrome fibroblasts. Interestingly, differentially methylated regions identified CERS1 and CERS3, two members of the ceramide synthase family. Moreover, we found differentially methylated probes within ITGA9 and ADAM12 genes, whose methylation is altered in systemic sclerosis, and within the PRDM8 gene, whose methylation is affected in dyskeratosis congenita and Down syndrome. Conclusions: DNA methylation changes in the peripheral blood from Werner syndrome patients provide new insight in the pathogenesis of the disease, highlighting in some cases a functional correlation of gene expression and methylation status.

Original languageEnglish
Article number92
JournalClinical Epigenetics
Volume9
Issue number1
DOIs
Publication statusPublished - Aug 30 2017

Fingerprint

Werner Syndrome
DNA Methylation
Blood Cells
Genome
Methylation
Phenotype
Genes
Dyskeratosis Congenita
Glycosphingolipids
Focal Adhesions
Systemic Scleroderma
Down Syndrome
Phosphatidylinositol 3-Kinases
Epigenomics
Fibroblasts
Insulin
Gene Expression
Mutation

Keywords

  • DNA methylation
  • Systemic sclerosis
  • Werner syndrome

ASJC Scopus subject areas

  • Molecular Biology
  • Genetics
  • Developmental Biology
  • Genetics(clinical)

Cite this

Genome-wide DNA methylation analysis in blood cells from patients with Werner syndrome. / Guastafierro, T.; Bacalini, M. G.; Marcoccia, A.; Gentilini, D.; Pisoni, S.; Di Blasio, A. M.; Corsi, A.; Franceschi, C.; Raimondo, D.; Spanò, A.; Garagnani, P.; Bondanini, F.

In: Clinical Epigenetics, Vol. 9, No. 1, 92, 30.08.2017.

Research output: Contribution to journalArticle

Guastafierro, T, Bacalini, MG, Marcoccia, A, Gentilini, D, Pisoni, S, Di Blasio, AM, Corsi, A, Franceschi, C, Raimondo, D, Spanò, A, Garagnani, P & Bondanini, F 2017, 'Genome-wide DNA methylation analysis in blood cells from patients with Werner syndrome', Clinical Epigenetics, vol. 9, no. 1, 92. https://doi.org/10.1186/s13148-017-0389-4
Guastafierro, T. ; Bacalini, M. G. ; Marcoccia, A. ; Gentilini, D. ; Pisoni, S. ; Di Blasio, A. M. ; Corsi, A. ; Franceschi, C. ; Raimondo, D. ; Spanò, A. ; Garagnani, P. ; Bondanini, F. / Genome-wide DNA methylation analysis in blood cells from patients with Werner syndrome. In: Clinical Epigenetics. 2017 ; Vol. 9, No. 1.
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