DNA Methylation Signature of Aging: Potential Impact on the Pathogenesis of Parkinson's Disease.
DNA Methylation Signature of Aging: Potential Impact on the Pathogenesis of Parkinson's Disease.
复制标题
衰老的DNA甲基化特征:对帕金森氏病的发病机理的潜在影响。
DOI:
10.3233/jpd-223517
复制
发表时间:
2023
期刊:
影响因子:
--
通讯作者:
Kang SU
中科院分区:
文献类型:
--
作者:
Yazar V;Dawson VL;Dawson TM;Kang SU
Regulation of gene expression by epigenetic modifications means lasting and heritable changes in the function of genes without alterations in the DNA sequence. Of all epigenetic mechanisms identified thus far, DNA methylation has been of particular interest in both aging and age-related disease research over the last decade given the consistency of site-specific DNA methylation changes during aging that can predict future health and lifespan. An increasing line of evidence has implied the dynamic nature of DNA (de)methylation events that occur throughout the lifespan has a role in the pathophysiology of aging and age-associated neurodegenerative conditions, including Parkinson’s disease (PD). In this regard, PD methylome shows, to some extent, similar genome-wide changes observed in the methylome of healthy individuals of matching age. In this review, we start by providing a brief overview of studies outlining global patterns of DNA methylation, then its mechanisms and regulation, within the context of aging and PD. Considering diverging lines of evidence from different experimental and animal models of neurodegeneration and how they combine to shape our current understanding of tissue-specific changes in DNA methylome in health and disease, we report a high-level comparison of the genomic methylation landscapes of brain, with an emphasis on dopaminergic neurons in PD and in natural aging. We believe this will be particularly useful for systematically dissecting overlapping genome-wide alterations in DNA methylation during PD and healthy aging, and for improving our knowledge of PD-specific changes in methylation patterns independent of aging process.
影响因子:
3.7
作者:
Ciccarone F;Klinger FG;Catizone A;Calabrese R;Zampieri M;Bacalini MG;De Felici M;Caiafa P
通讯作者:
Caiafa P
DOI:
10.1016/j.mcn.2017.11.002
发表时间:
2018-01
期刊:
Molecular and cellular neurosciences
影响因子:
--
作者:
Lardenoije R;van den Hove DLA;Havermans M;van Casteren A;Le KX;Palmour R;Lemere CA;Rutten BPF
通讯作者:
Rutten BPF