Abstract | PURPOSE OF REVIEW: RECENT FINDINGS: Within the last two years, genome-wide association (GWA) analyses have revealed a number of novel low-risk susceptibility variants for Parkinson's disease, among them HLA-DRB5, BST1, ACMSD, STK39, MCCC1/LAMP3, SYT11, and CCDC62/HIP1R) and have confirmed LINGO1 as risk factor for essential tremor. The identification of copy number variations in the Parkin gene in healthy control individuals suggests no major role of these variations in late onset Parkinson's disease. Drosophila studies on Parkin and Pink1 have uncovered a role in the mitochondrial quality control pathway in the pathogenesis of the disease. LRRK2 has been found to interact with the microRNAs processing protein Argonaut, thereby affecting protein translation. Notably, despite the high familial risk for essential tremor no high-risk gene has been found to date. The possibility of a nonmendelian transmission in some cases is discussed. SUMMARY: GWA studies and positional cloning approaches have led to the identification of a number of risk genes for Parkinson's disease, which give novel insights into pathogenic pathways of the disease. In contrast, our knowledge of the genetics of essential tremor is scarce. Except for LINGO1, no other risk gene has so far been identified. New technologies such as next generation high throughput sequencing might help to identify more risk genes.
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Authors | Alexander Zimprich |
Journal | Current opinion in neurology
(Curr Opin Neurol)
Vol. 24
Issue 4
Pg. 318-23
(Aug 2011)
ISSN: 1473-6551 [Electronic] England |
PMID | 21734494
(Publication Type: Journal Article, Review)
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Chemical References |
- LINGO1 protein, human
- Membrane Proteins
- Nerve Tissue Proteins
- Ubiquitin-Protein Ligases
- parkin protein
- Protein Kinases
- LRRK2 protein, human
- Leucine-Rich Repeat Serine-Threonine Protein Kinase-2
- PTEN-induced putative kinase
- Protein Serine-Threonine Kinases
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Topics |
- Animals
- Essential Tremor
(genetics)
- Genetic Linkage
- Genome-Wide Association Study
- Humans
- Leucine-Rich Repeat Serine-Threonine Protein Kinase-2
- Membrane Proteins
(genetics)
- Mutation
- Nerve Tissue Proteins
(genetics)
- Parkinson Disease
(genetics)
- Protein Kinases
(genetics)
- Protein Serine-Threonine Kinases
(genetics)
- Risk Factors
- Ubiquitin-Protein Ligases
(genetics)
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