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Age-associated DNA methylation changes in immune genes, histone modifiers and chromatin remodeling factors within 5 years after birth in human blood leukocytes

BACKGROUND: Age-related changes in DNA methylation occurring in blood leukocytes during early childhood may reflect epigenetic maturation. We hypothesized that some of these changes involve gene networks of critical relevance in leukocyte biology and conducted a prospective study to elucidate the dy...

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Autores principales: Acevedo, Nathalie, Reinius, Lovisa E, Vitezic, Morana, Fortino, Vittorio, Söderhäll, Cilla, Honkanen, Hanna, Veijola, Riitta, Simell, Olli, Toppari, Jorma, Ilonen, Jorma, Knip, Mikael, Scheynius, Annika, Hyöty, Heikki, Greco, Dario, Kere, Juha
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4396570/
https://www.ncbi.nlm.nih.gov/pubmed/25874017
http://dx.doi.org/10.1186/s13148-015-0064-6
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author Acevedo, Nathalie
Reinius, Lovisa E
Vitezic, Morana
Fortino, Vittorio
Söderhäll, Cilla
Honkanen, Hanna
Veijola, Riitta
Simell, Olli
Toppari, Jorma
Ilonen, Jorma
Knip, Mikael
Scheynius, Annika
Hyöty, Heikki
Greco, Dario
Kere, Juha
author_facet Acevedo, Nathalie
Reinius, Lovisa E
Vitezic, Morana
Fortino, Vittorio
Söderhäll, Cilla
Honkanen, Hanna
Veijola, Riitta
Simell, Olli
Toppari, Jorma
Ilonen, Jorma
Knip, Mikael
Scheynius, Annika
Hyöty, Heikki
Greco, Dario
Kere, Juha
author_sort Acevedo, Nathalie
collection PubMed
description BACKGROUND: Age-related changes in DNA methylation occurring in blood leukocytes during early childhood may reflect epigenetic maturation. We hypothesized that some of these changes involve gene networks of critical relevance in leukocyte biology and conducted a prospective study to elucidate the dynamics of DNA methylation. Serial blood samples were collected at 3, 6, 12, 24, 36, 48 and 60 months after birth in ten healthy girls born in Finland and participating in the Type 1 Diabetes Prediction and Prevention Study. DNA methylation was measured using the HumanMethylation450 BeadChip. RESULTS: After filtering for the presence of polymorphisms and cell-lineage-specific signatures, 794 CpG sites showed significant DNA methylation differences as a function of age in all children (41.6% age-methylated and 58.4% age-demethylated, Bonferroni-corrected P value <0.01). Age-methylated CpGs were more frequently located in gene bodies and within +5 to +50 kilobases (kb) of transcription start sites (TSS) and enriched in developmental, neuronal and plasma membrane genes. Age-demethylated CpGs were associated to promoters and DNAse-I hypersensitivity sites, located within −5 to +5 kb of the nearest TSS and enriched in genes related to immunity, antigen presentation, the polycomb-group protein complex and cytoplasm. CONCLUSIONS: This study reveals that susceptibility loci for complex inflammatory diseases (for example, IRF5, NOD2, and PTGER4) and genes encoding histone modifiers and chromatin remodeling factors (for example, HDAC4, KDM2A, KDM2B, JARID2, ARID3A, and SMARCD3) undergo DNA methylation changes in leukocytes during early childhood. These results open new perspectives to understand leukocyte maturation and provide a catalogue of CpG sites that may need to be corrected for age effects when performing DNA methylation studies in children. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13148-015-0064-6) contains supplementary material, which is available to authorized users.
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spelling pubmed-43965702015-04-15 Age-associated DNA methylation changes in immune genes, histone modifiers and chromatin remodeling factors within 5 years after birth in human blood leukocytes Acevedo, Nathalie Reinius, Lovisa E Vitezic, Morana Fortino, Vittorio Söderhäll, Cilla Honkanen, Hanna Veijola, Riitta Simell, Olli Toppari, Jorma Ilonen, Jorma Knip, Mikael Scheynius, Annika Hyöty, Heikki Greco, Dario Kere, Juha Clin Epigenetics Research BACKGROUND: Age-related changes in DNA methylation occurring in blood leukocytes during early childhood may reflect epigenetic maturation. We hypothesized that some of these changes involve gene networks of critical relevance in leukocyte biology and conducted a prospective study to elucidate the dynamics of DNA methylation. Serial blood samples were collected at 3, 6, 12, 24, 36, 48 and 60 months after birth in ten healthy girls born in Finland and participating in the Type 1 Diabetes Prediction and Prevention Study. DNA methylation was measured using the HumanMethylation450 BeadChip. RESULTS: After filtering for the presence of polymorphisms and cell-lineage-specific signatures, 794 CpG sites showed significant DNA methylation differences as a function of age in all children (41.6% age-methylated and 58.4% age-demethylated, Bonferroni-corrected P value <0.01). Age-methylated CpGs were more frequently located in gene bodies and within +5 to +50 kilobases (kb) of transcription start sites (TSS) and enriched in developmental, neuronal and plasma membrane genes. Age-demethylated CpGs were associated to promoters and DNAse-I hypersensitivity sites, located within −5 to +5 kb of the nearest TSS and enriched in genes related to immunity, antigen presentation, the polycomb-group protein complex and cytoplasm. CONCLUSIONS: This study reveals that susceptibility loci for complex inflammatory diseases (for example, IRF5, NOD2, and PTGER4) and genes encoding histone modifiers and chromatin remodeling factors (for example, HDAC4, KDM2A, KDM2B, JARID2, ARID3A, and SMARCD3) undergo DNA methylation changes in leukocytes during early childhood. These results open new perspectives to understand leukocyte maturation and provide a catalogue of CpG sites that may need to be corrected for age effects when performing DNA methylation studies in children. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13148-015-0064-6) contains supplementary material, which is available to authorized users. BioMed Central 2015-03-26 /pmc/articles/PMC4396570/ /pubmed/25874017 http://dx.doi.org/10.1186/s13148-015-0064-6 Text en © Acevedo et al.; licensee BioMed Central. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Acevedo, Nathalie
Reinius, Lovisa E
Vitezic, Morana
Fortino, Vittorio
Söderhäll, Cilla
Honkanen, Hanna
Veijola, Riitta
Simell, Olli
Toppari, Jorma
Ilonen, Jorma
Knip, Mikael
Scheynius, Annika
Hyöty, Heikki
Greco, Dario
Kere, Juha
Age-associated DNA methylation changes in immune genes, histone modifiers and chromatin remodeling factors within 5 years after birth in human blood leukocytes
title Age-associated DNA methylation changes in immune genes, histone modifiers and chromatin remodeling factors within 5 years after birth in human blood leukocytes
title_full Age-associated DNA methylation changes in immune genes, histone modifiers and chromatin remodeling factors within 5 years after birth in human blood leukocytes
title_fullStr Age-associated DNA methylation changes in immune genes, histone modifiers and chromatin remodeling factors within 5 years after birth in human blood leukocytes
title_full_unstemmed Age-associated DNA methylation changes in immune genes, histone modifiers and chromatin remodeling factors within 5 years after birth in human blood leukocytes
title_short Age-associated DNA methylation changes in immune genes, histone modifiers and chromatin remodeling factors within 5 years after birth in human blood leukocytes
title_sort age-associated dna methylation changes in immune genes, histone modifiers and chromatin remodeling factors within 5 years after birth in human blood leukocytes
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4396570/
https://www.ncbi.nlm.nih.gov/pubmed/25874017
http://dx.doi.org/10.1186/s13148-015-0064-6
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