Cited by 107Parkinson's Disease Mechanisms and TreatmentsEpigenetics and DNA MethylationNuclear Receptors and Signaling

DNA methylation in Parkinson's disease

Open access
Wüllner, Ullrich, Kaut, Oliver, deBoni, Laura, Piston, Dominik, Schmitt, Ina·2016·Journal of Neurochemistry

Abstract

Epigenetic processes control the embryonic development into multicellular organisms and determine the functional differences of genetically identical cells and individuals. They are also involved in a variety of complex functions such as learning and memory consolidation and have been implicated in aging processes. Beyond the actual genetic information encoded in the DNA sequence, epigenetic modifications in particular DNA methylation and various histone modifications shape the chromatin into a transcriptional permissive or repressive state. DNA methylation patterns are altered by environmental conditions and can be carried forward through mitosis and meiosis. Hence, DNA methylation probably mediates complex environment–gene interactions, determines individual disease characteristics, and contributes to effects and side effects of drugs. In addition to classic monogenic epigenetic diseases, i.e., Prader‐Willi and Rett syndrome, recent data point to an epigenetic component also in apparent sporadic neuro‐psychiatric disorders and increasing evidence suggests a role for altered DNA methylation in Parkinson's disease. Epigenetic alterations, DNA methylation in particular, may account for the yet unexplained individual susceptibility and the variability in the course of Parkinson's disease and could provide hints toward the development of novel therapeutic targets. image Parkinson's disease (PD) is conceptualized as a consequence of genetic variants and environment–gene interactions on a background of age‐related changes. Epigenetic modifications have been implicated in aging and can be altered by environment stimuli. The review explores the possibility of an epigenetic component in PD, focusing on DNA methylation. Methylation of α‐synuclein (SNCA) and microtubule‐associated protein tau gene appear to be of particular importance and epigenome‐wide methylation studies point to several additional candidate genes which may contribute to the individual susceptibility toward PD. This article is part of a special issue on Parkinson disease.

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  • The contribution of epigenetic modifications to neurodegenerative diseases such as PD and AD has been addressed in a number of studies.

    “Indeed, the contribution of epigenetic modifications to neurodegenerative diseases such as PD (Wüllner et al., 2016) (Park et al., 2015) and AD (Watson et al., 2016), (Phipps et al., 2016) has been addressed in a number of studies.”

    From TET2 Regulates the Neuroinflammatory Response in Microglia (2019) · cites this paper as Wüllner et al., 2016

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  1. Booth M. J., Ost T. W. B., Beraldi D., Bell N. M., Branco M. R., Reik W. and Balasubramanian S. (2013) Oxidative bisulfite sequencing of 5-methylcytosine and 5-hydroxymethylcytosine. Nat. Protoc. 8, 1841-1851. doi:10.1038/nprot.2013.115. · DOI
  2. Heijmans B. T., Tobi E. W., Stein A. D., Putter H., Blauw G. J., Susser E. S., Slagboom P. E. and Lumey L. H. (2008) Persistent epigenetic differences associated with prenatal exposure to famine in humans. Proc. Natl Acad. Sci. USA 105, 17046-17049.
  3. Koh K. P., Yabuuchi A., Rao S. et al. , 2011. Tet1 and Tet2 regulate 5- hydroxymethylcytosine production and cell lineage specification in mouse embryonic stem cells. Cell Stem Cell 8, 200-213. doi:10.1016/j.stem.2011.01.008 · DOI · Paper page
  4. Wirdefeldt K., Adami H. O., Cole P., Trichopoulos D. and Mandel J. (2011) Epidemiology and etiology of Parkinson's disease: a review of the evidence. Eur. J. Epidemiol. 1, 51-58.

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Authors
Wüllner, U., Kaut, O., deBoni, L., Piston, D., & Schmitt, I.
Affiliations
  • University of Bonn (DE)
  • German Center for Neurodegenerative Diseases (DZNE) and Department of Neurology University of Bonn Bonn Germany
Corresponding author
Wüllner, Ullrich
Venue
Journal of Neurochemistry
Publisher
Wiley
Published
2016-06-10
Volume
139
Issue
S1
Pages
108-120
ISSN
  • 0022-3042 (ISSN-L)
  • 1471-4159
OpenAlex
W2342685421
Cited by
107
References
13
Citations by year
2026: 5 · 2025: 9 · 2024: 14 · 2023: 13 · 2022: 9 · 2021: 16 · 2020: 13 · 2019: 12 · 2018: 5 · 2017: 7 · 2016: 4
FWCI
1.30
Type
journal article
Language
en
Open access
Locations
  • Journal of Neurochemistry (publishedVersion)
  • PubMed (publishedVersion)
  • DZNE Pub (submittedVersion)
Funders
  • EU/EFPIA Innovative Medicines Initiative Joint Undertaking (115568)
  • Epigenomics of Common and Age-related Diseases Programme (01KU1403B)
  • ParkinsonFonds Deutschland gGmbH
  • Deutsche Parkinson Vereinigung (dPV)
Topics
  • Health Sciences › Medicine › Neurology › Parkinson's Disease Mechanisms and Treatments
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Epigenetics and DNA Methylation
  • Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Nuclear Receptors and Signaling
Keywords
DNA methylation, Parkinson's disease, epigenetics, alpha-synuclein, SNCA, tau gene, tau protein, aging, histone modifications, chromatin, therapeutic target
MeSH terms
Aging, Animals, Humans, Parkinson Disease, DNA Methylation, Epigenesis, Genetic, Ubiquitin-Protein Ligases, alpha-Synuclein

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