Abstract
Until recently, genetics was thought to play a minor role in the development of Parkinson's disease (PD). Over the last decade, a number of genes that definitively cause PD have been identified, which has led to the generation of disease models based on pathogenic gene variants that recapitulate many features of the disease. These genetic studies have provided novel insight into potential mechanisms underlying the aetiology of PD. This chapter will provide a profile of the genes conclusively linked to PD and will outline the mechanisms of PD pathogenesis implicated by genetic studies. Mitochondrial dysfunction, oxidative stress and impaired ubiquitin-proteasome system function are disease mechanisms that are particularly well supported by genetic studies and are therefore the focus of this chapter.
2010 Elsevier B.V. All rights reserved.
Publication types
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Research Support, N.I.H., Extramural
MeSH terms
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Humans
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Intracellular Signaling Peptides and Proteins / genetics
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Leucine-Rich Repeat Serine-Threonine Protein Kinase-2
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Mitochondrial Diseases / complications
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Mitochondrial Diseases / genetics*
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Mutation / genetics*
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Oncogene Proteins / genetics
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Oxidative Stress / genetics*
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Parkinson Disease / etiology
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Parkinson Disease / genetics*
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Parkinson Disease / physiopathology
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Protein Deglycase DJ-1
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Protein Kinases / genetics
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Protein Serine-Threonine Kinases / genetics
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Ubiquitin-Protein Ligase Complexes / genetics*
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Ubiquitin-Protein Ligases / genetics
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alpha-Synuclein / genetics
Substances
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Intracellular Signaling Peptides and Proteins
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Oncogene Proteins
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alpha-Synuclein
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Ubiquitin-Protein Ligase Complexes
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Ubiquitin-Protein Ligases
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parkin protein
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Protein Kinases
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LRRK2 protein, human
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Leucine-Rich Repeat Serine-Threonine Protein Kinase-2
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PTEN-induced putative kinase
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Protein Serine-Threonine Kinases
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PARK7 protein, human
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Protein Deglycase DJ-1