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Science 27 June 1997: Vol. 276. no. 5321, pp. 2045 - 2047 DOI: 10.1126/science.276.5321.2045
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Reports
Mutation in the -Synuclein Gene Identified in Families with Parkinson's Disease
Mihael H. Polymeropoulos,
*
Christian Lavedan,
Elisabeth Leroy,
Susan E. Ide,
Anindya Dehejia,
Amalia Dutra,
Brian Pike,
Holly Root,
Jeffrey Rubenstein,
Rebecca Boyer,
Edward S. Stenroos,
Settara Chandrasekharappa,
Aglaia Athanassiadou,
Theodore Papapetropoulos,
William G. Johnson,
Alice M. Lazzarini,
Roger C. Duvoisin,
Giuseppe Di Iorio,
Lawrence I. Golbe,
Robert
L. Nussbaum
Parkinson's disease (PD) is a common neurodegenerative
disorder with a lifetime incidence of approximately 2 percent. A
pattern of familial aggregation has been documented for the disorder, and it was recently reported that a PD susceptibility gene in a large
Italian kindred is located on the long arm of human chromosome 4. A
mutation was identified in the -synuclein gene, which codes for a
presynaptic protein thought to be involved in neuronal plasticity, in
the Italian kindred and in three unrelated families of Greek origin
with autosomal dominant inheritance for the PD phenotype. This finding
of a specific molecular alteration associated with PD will facilitate
the detailed understanding of the pathophysiology of the disorder.
M. H. Polymeropoulos, C. Lavedan, E. Leroy, S. E. Ide, A. Dehejia,
J. Rubenstein, R. Boyer, R. L. Nussbaum, Laboratory of Genetic Disease
Research, National Human Genome Research Institute, National Institutes
of Health, Bethesda, MD 20892-1430, USA.
S. Chandrasekharappa, B. Pike, H. Root, A. Dutra, Laboratory of Gene
Transfer, National Human Genome Research Institute, National Institutes
of Health, Bethesda, MD 20892-1430, USA.
L. I. Golbe, W. G. Johnson, E. S. Stenroos, R. C. Duvoisin, A. M. Lazzarini, University of Medicine and Dentistry of New Jersey, Robert
Wood Johnson Medical School, Piscataway, NJ 08854, USA.
G. Di Iorio, Instituto di Scienze Neurologiche, Faculta di Medicina,
Seconda Universita degli Studi di Napoli, Naples, Italy.
T. Papapetropoulos and A. Athanassiadou, University of Patras Medical
School, Patras, Greece.
*
To whom correspondence should be addressed.
These authors contributed equally in this work.
Read the Full Text
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- Investigation of {alpha}-Synuclein Fibril Structure by Site-directed Spin Labeling.
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282, 24970-24979
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- Different Species of {alpha}-Synuclein Oligomers Induce Calcium Influx and Seeding.
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- YGR198w (YPP1) targets A30P {alpha}-synuclein to the vacuole for degradation.
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- Nonparametric estimation of age-at-onset distributions from censored kin-cohort data.
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Biometrika
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- Merging Mouse Transcriptome Analyses with Parkinson's Disease Linkage Studies.
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DNA Res
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- Individual dopaminergic neurons show raised iron levels in Parkinson disease.
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Neurology
68, 1820-1825
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- A cell biological perspective on mitochondrial dysfunction in Parkinson disease and other neurodegenerative diseases.
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J. Cell Sci.
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- Assembly of Lysine 63-linked Ubiquitin Conjugates by Phosphorylated {alpha}-Synuclein Implies Lewy Body Biogenesis.
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282, 14558-14566
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- Identification of Novel Proteins Associated with Both {alpha}-Synuclein and DJ-1.
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Mol. Cell. Proteomics
6, 845-859
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- Thioredoxin Suppresses Parkin-associated Endothelin Receptor-like Receptor-induced Neurotoxicity and Extends Longevity in Drosophila.
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282, 11180-11187
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- Translocation of {alpha}-Synuclein Expressed in Escherichia coli.
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- Aggregated {alpha}-Synuclein Mediates Dopaminergic Neurotoxicity In Vivo.
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- Over-expression of alpha-synuclein in human neural progenitors leads to specific changes in fate and differentiation.
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Hum. Mol. Genet.
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- DLB and PDD boundary issues: Diagnosis, treatment, molecular pathology, and biomarkers.
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Neurology
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- Emerging Roles for Ubiquitin and Protein Degradation in Neuronal Function.
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- Long-term consequences of human alpha-synuclein overexpression in the primate ventral midbrain.
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Brain
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- Trehalose, a Novel mTOR-independent Autophagy Enhancer, Accelerates the Clearance of Mutant Huntingtin and {alpha}-Synuclein.
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