Cargando…

Methylation of the ribosomal RNA gene promoter is associated with aging and age‐related decline

The transcription of ribosomal RNA genes (rDNA) is subject to epigenetic regulation, as it is abrogated by the methylation of CpG dinucleotides within their promoter region. Here, we investigated, through Sequenom platform, the age‐related methylation status of the CpG island falling into the rDNA p...

Descripción completa

Detalles Bibliográficos
Autores principales: D'Aquila, Patrizia, Montesanto, Alberto, Mandalà, Maurizio, Garasto, Sabrina, Mari, Vincenzo, Corsonello, Andrea, Bellizzi, Dina, Passarino, Giuseppe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5595699/
https://www.ncbi.nlm.nih.gov/pubmed/28625020
http://dx.doi.org/10.1111/acel.12603
_version_ 1783263407407890432
author D'Aquila, Patrizia
Montesanto, Alberto
Mandalà, Maurizio
Garasto, Sabrina
Mari, Vincenzo
Corsonello, Andrea
Bellizzi, Dina
Passarino, Giuseppe
author_facet D'Aquila, Patrizia
Montesanto, Alberto
Mandalà, Maurizio
Garasto, Sabrina
Mari, Vincenzo
Corsonello, Andrea
Bellizzi, Dina
Passarino, Giuseppe
author_sort D'Aquila, Patrizia
collection PubMed
description The transcription of ribosomal RNA genes (rDNA) is subject to epigenetic regulation, as it is abrogated by the methylation of CpG dinucleotides within their promoter region. Here, we investigated, through Sequenom platform, the age‐related methylation status of the CpG island falling into the rDNA promoter in 472 blood samples from 20‐ to 105‐year‐old humans and in different tissues (blood, heart, liver, kidney, and testis) of 15 rats 3–96 weeks old. In humans, we did not find a consistently significant correlation between CpG site methylation and chronological age. Furthermore, the methylation levels of one of the analyzed CpG sites were negatively associated with both cognitive performance and survival chance measured in a 9‐year follow‐up study. We consistently confirmed such result in a replication sample. In rats, the analysis of the homologous region in the tissues revealed the existence of increased methylation in old rats. rRNA expression data, in both humans and rats, were consistent with observed methylation patterns, with a lower expression of rRNA in highly methylated samples. As chronological and biological ages in rats of a given strain are likely to be much closer to each other than in humans, these results seem to provide the first evidence that epigenetic modifications of rDNA change over time according to the aging decline. Thus, the methylation profile of rDNA may represent a potential biomarker of aging.
format Online
Article
Text
id pubmed-5595699
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-55956992017-10-01 Methylation of the ribosomal RNA gene promoter is associated with aging and age‐related decline D'Aquila, Patrizia Montesanto, Alberto Mandalà, Maurizio Garasto, Sabrina Mari, Vincenzo Corsonello, Andrea Bellizzi, Dina Passarino, Giuseppe Aging Cell Original Articles The transcription of ribosomal RNA genes (rDNA) is subject to epigenetic regulation, as it is abrogated by the methylation of CpG dinucleotides within their promoter region. Here, we investigated, through Sequenom platform, the age‐related methylation status of the CpG island falling into the rDNA promoter in 472 blood samples from 20‐ to 105‐year‐old humans and in different tissues (blood, heart, liver, kidney, and testis) of 15 rats 3–96 weeks old. In humans, we did not find a consistently significant correlation between CpG site methylation and chronological age. Furthermore, the methylation levels of one of the analyzed CpG sites were negatively associated with both cognitive performance and survival chance measured in a 9‐year follow‐up study. We consistently confirmed such result in a replication sample. In rats, the analysis of the homologous region in the tissues revealed the existence of increased methylation in old rats. rRNA expression data, in both humans and rats, were consistent with observed methylation patterns, with a lower expression of rRNA in highly methylated samples. As chronological and biological ages in rats of a given strain are likely to be much closer to each other than in humans, these results seem to provide the first evidence that epigenetic modifications of rDNA change over time according to the aging decline. Thus, the methylation profile of rDNA may represent a potential biomarker of aging. John Wiley and Sons Inc. 2017-06-17 2017-10 /pmc/articles/PMC5595699/ /pubmed/28625020 http://dx.doi.org/10.1111/acel.12603 Text en © 2017 The Authors. Aging Cell published by the Anatomical Society and John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
D'Aquila, Patrizia
Montesanto, Alberto
Mandalà, Maurizio
Garasto, Sabrina
Mari, Vincenzo
Corsonello, Andrea
Bellizzi, Dina
Passarino, Giuseppe
Methylation of the ribosomal RNA gene promoter is associated with aging and age‐related decline
title Methylation of the ribosomal RNA gene promoter is associated with aging and age‐related decline
title_full Methylation of the ribosomal RNA gene promoter is associated with aging and age‐related decline
title_fullStr Methylation of the ribosomal RNA gene promoter is associated with aging and age‐related decline
title_full_unstemmed Methylation of the ribosomal RNA gene promoter is associated with aging and age‐related decline
title_short Methylation of the ribosomal RNA gene promoter is associated with aging and age‐related decline
title_sort methylation of the ribosomal rna gene promoter is associated with aging and age‐related decline
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5595699/
https://www.ncbi.nlm.nih.gov/pubmed/28625020
http://dx.doi.org/10.1111/acel.12603
work_keys_str_mv AT daquilapatrizia methylationoftheribosomalrnagenepromoterisassociatedwithagingandagerelateddecline
AT montesantoalberto methylationoftheribosomalrnagenepromoterisassociatedwithagingandagerelateddecline
AT mandalamaurizio methylationoftheribosomalrnagenepromoterisassociatedwithagingandagerelateddecline
AT garastosabrina methylationoftheribosomalrnagenepromoterisassociatedwithagingandagerelateddecline
AT marivincenzo methylationoftheribosomalrnagenepromoterisassociatedwithagingandagerelateddecline
AT corsonelloandrea methylationoftheribosomalrnagenepromoterisassociatedwithagingandagerelateddecline
AT bellizzidina methylationoftheribosomalrnagenepromoterisassociatedwithagingandagerelateddecline
AT passarinogiuseppe methylationoftheribosomalrnagenepromoterisassociatedwithagingandagerelateddecline