作者
Simone Engelender, Zachary Kaminsky, Xin Guo, Alan H Sharp, Ravi K Amaravi, John J Kleiderlein, Russell L Margolis, Juan C Troncoso, Anthony A Lanahan, Paul F Worley, Valina L Dawson, Ted M Dawson, Christopher A Ross
发表日期
1999/5
期刊
Nature genetics
卷号
22
期号
1
页码范围
110-114
出版商
Nature Publishing Group
简介
Parkinson disease (PD) is a neurodegenerative disease characterized by tremor, bradykinesia, rigidity and postural instability. Post-mortem examination shows loss of neurons and Lewy bodies, which are cytoplasmic eosinophilic inclusions, in the substantia nigra and other brain regions 1, 2. A few families have PD caused by mutations (A53T or A30P) in the gene SNCA (encoding α-synuclein; refs 3, 4, 5). α-synuclein is present in Lewy bodies of patients with sporadic PD (Refs 6, 7), suggesting that α-synuclein may be involved in the pathogenesis of PD. It is unknown how α-synuclein contributes to the cellular and biochemical mechanisms of PD, and its normal functions and biochemical properties are poorly understood 8, 9, 10. To determine the protein-interaction partners of α-synuclein, we performed a yeast two-hybrid screen. We identified a novel interacting protein, which we term synphilin-1 (encoded by the …
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