Environmental and Genetic Variables Influencing Mitochondrial Health and Parkinson’s Disease Penetrance

There is strong evidence that impairment of mitochondrial function plays a key role in the pathogenesis of PD. The two key PD genes related to mitochondrial function are Parkin (PARK2) and PINK1 (PARK6), and also mutations in several other PD genes, including SNCA, LRRK2, DJ1, CHCHD2, and POLG, have...

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Main Authors: Alessandra Zanon, Peter P. Pramstaller, Andrew A. Hicks, Irene Pichler
Format: Article
Language:English
Published: Wiley 2018-01-01
Series:Parkinson's Disease
Online Access:http://dx.doi.org/10.1155/2018/8684906
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author Alessandra Zanon
Peter P. Pramstaller
Andrew A. Hicks
Irene Pichler
author_facet Alessandra Zanon
Peter P. Pramstaller
Andrew A. Hicks
Irene Pichler
author_sort Alessandra Zanon
collection DOAJ
description There is strong evidence that impairment of mitochondrial function plays a key role in the pathogenesis of PD. The two key PD genes related to mitochondrial function are Parkin (PARK2) and PINK1 (PARK6), and also mutations in several other PD genes, including SNCA, LRRK2, DJ1, CHCHD2, and POLG, have been shown to induce mitochondrial stress. Many mutations are clearly pathogenic in some patients while carriers of other mutations either do not develop the disease or show a delayed onset, a phenomenon known as reduced penetrance. Indeed, for several mutations in autosomal dominant PD genes, penetrance is markedly reduced, whereas heterozygous carriers of recessive mutations may predispose to PD in a dominant manner, although with highly reduced penetrance, if additional disease modifiers are present. The identification and validation of such modifiers leading to reduced penetrance or increased susceptibility in the case of heterozygous carriers of recessive mutations are relevant for a better understanding of mechanisms contributing to disease onset. We discuss genetic and environmental factors as well as mitochondrial DNA alterations and protein-protein interactions, all involved in mitochondrial function, as potential causes to modify penetrance of mutations in dominant PD genes and to determine manifestation of heterozygous mutations in recessive PD genes.
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series Parkinson's Disease
spelling doaj-art-d9451d50662e4dba9145d0650c3c868c2025-02-03T01:21:53ZengWileyParkinson's Disease2090-80832042-00802018-01-01201810.1155/2018/86849068684906Environmental and Genetic Variables Influencing Mitochondrial Health and Parkinson’s Disease PenetranceAlessandra Zanon0Peter P. Pramstaller1Andrew A. Hicks2Irene Pichler3Institute for Biomedicine, Eurac Research, Affiliated Institute of the University of Lübeck, Bolzano, ItalyInstitute for Biomedicine, Eurac Research, Affiliated Institute of the University of Lübeck, Bolzano, ItalyInstitute for Biomedicine, Eurac Research, Affiliated Institute of the University of Lübeck, Bolzano, ItalyInstitute for Biomedicine, Eurac Research, Affiliated Institute of the University of Lübeck, Bolzano, ItalyThere is strong evidence that impairment of mitochondrial function plays a key role in the pathogenesis of PD. The two key PD genes related to mitochondrial function are Parkin (PARK2) and PINK1 (PARK6), and also mutations in several other PD genes, including SNCA, LRRK2, DJ1, CHCHD2, and POLG, have been shown to induce mitochondrial stress. Many mutations are clearly pathogenic in some patients while carriers of other mutations either do not develop the disease or show a delayed onset, a phenomenon known as reduced penetrance. Indeed, for several mutations in autosomal dominant PD genes, penetrance is markedly reduced, whereas heterozygous carriers of recessive mutations may predispose to PD in a dominant manner, although with highly reduced penetrance, if additional disease modifiers are present. The identification and validation of such modifiers leading to reduced penetrance or increased susceptibility in the case of heterozygous carriers of recessive mutations are relevant for a better understanding of mechanisms contributing to disease onset. We discuss genetic and environmental factors as well as mitochondrial DNA alterations and protein-protein interactions, all involved in mitochondrial function, as potential causes to modify penetrance of mutations in dominant PD genes and to determine manifestation of heterozygous mutations in recessive PD genes.http://dx.doi.org/10.1155/2018/8684906
spellingShingle Alessandra Zanon
Peter P. Pramstaller
Andrew A. Hicks
Irene Pichler
Environmental and Genetic Variables Influencing Mitochondrial Health and Parkinson’s Disease Penetrance
Parkinson's Disease
title Environmental and Genetic Variables Influencing Mitochondrial Health and Parkinson’s Disease Penetrance
title_full Environmental and Genetic Variables Influencing Mitochondrial Health and Parkinson’s Disease Penetrance
title_fullStr Environmental and Genetic Variables Influencing Mitochondrial Health and Parkinson’s Disease Penetrance
title_full_unstemmed Environmental and Genetic Variables Influencing Mitochondrial Health and Parkinson’s Disease Penetrance
title_short Environmental and Genetic Variables Influencing Mitochondrial Health and Parkinson’s Disease Penetrance
title_sort environmental and genetic variables influencing mitochondrial health and parkinson s disease penetrance
url http://dx.doi.org/10.1155/2018/8684906
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AT irenepichler environmentalandgeneticvariablesinfluencingmitochondrialhealthandparkinsonsdiseasepenetrance