TY - JOUR
T1 - Inefficient DNA Repair Is an Aging-Related Modifier of Parkinson's Disease
AU - Sepe, Sara
AU - Milanese, Chiara
AU - Gabriels, Sylvia
AU - Derks, Kasper W.J.
AU - Payan-Gomez, Cesar
AU - van IJcken, Wilfred F.J.
AU - Rijksen, Yvonne M.A.
AU - Nigg, Alex L.
AU - Moreno, Sandra
AU - Cerri, Silvia
AU - Blandini, Fabio
AU - Hoeijmakers, Jan H.J.
AU - Mastroberardino, Pier G.
N1 - Funding Information:
P.G.M. was supported by a grant from the Netherlands Genomics Initiative (NGI/NWO 05040202), a Marie Curie grant (IRG 247918), and the CEREBRAD grant under the EU-FP7 framework (project number 295552). The Extracellular Flux Analyzer by Seahorse Bioscience was purchased thanks to a generous donation from Dorpmans-Wigmans Stichting (to P.G.M.). J.H.J.H. acknowledges financial support from the NIH/National Institute of Aging (1PO1 AG-17242-02), the National Institute of Environmental Health Sciences (1UO1 ES011044), the Royal Academy of Arts and Sciences of the Netherlands (academia professorship), and a European Research Council Advanced Grant. C.M. was supported by the Ri.MED Foundation. The research leading to these results has received funding from the European Community’s Seventh Framework Programme (FP7/2007-2013) under grant agreement no. HEALTH-F2-2010-259893. C.P.G. is supported by ERACOL.
Publisher Copyright:
© 2016 The Author(s).
Copyright:
Copyright 2017 Elsevier B.V., All rights reserved.
PY - 2016/5/31
Y1 - 2016/5/31
N2 - The underlying relation between Parkinson's disease (PD) etiopathology and its major risk factor, aging, is largely unknown. In light of the causative link between genome stability and aging, we investigate a possible nexus between DNA damage accumulation, aging, and PD by assessing aging-related DNA repair pathways in laboratory animal models and humans. We demonstrate that dermal fibroblasts from PD patients display flawed nucleotide excision repair (NER) capacity and that Ercc1 mutant mice with mildly compromised NER exhibit typical PD-like pathological alterations, including decreased striatal dopaminergic innervation, increased phospho-synuclein levels, and defects in mitochondrial respiration. Ercc1 mouse mutants are also more sensitive to the prototypical PD toxin MPTP, and their transcriptomic landscape shares important similarities with that of PD patients. Our results demonstrate that specific defects in DNA repair impact the dopaminergic system and are associated with human PD pathology and might therefore constitute an age-related risk factor for PD.
AB - The underlying relation between Parkinson's disease (PD) etiopathology and its major risk factor, aging, is largely unknown. In light of the causative link between genome stability and aging, we investigate a possible nexus between DNA damage accumulation, aging, and PD by assessing aging-related DNA repair pathways in laboratory animal models and humans. We demonstrate that dermal fibroblasts from PD patients display flawed nucleotide excision repair (NER) capacity and that Ercc1 mutant mice with mildly compromised NER exhibit typical PD-like pathological alterations, including decreased striatal dopaminergic innervation, increased phospho-synuclein levels, and defects in mitochondrial respiration. Ercc1 mouse mutants are also more sensitive to the prototypical PD toxin MPTP, and their transcriptomic landscape shares important similarities with that of PD patients. Our results demonstrate that specific defects in DNA repair impact the dopaminergic system and are associated with human PD pathology and might therefore constitute an age-related risk factor for PD.
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U2 - 10.1016/j.celrep.2016.04.071
DO - 10.1016/j.celrep.2016.04.071
M3 - Research Article
C2 - 27210754
AN - SCOPUS:84971229247
SN - 2211-1247
VL - 15
SP - 1866
EP - 1875
JO - Cell Reports
JF - Cell Reports
IS - 9
ER -
