The rare inherited form of Parkinson's disease (PD), PARK5, is caused by a missense mutation in ubiquitin carboxy-terminal hydrolase-L1 (UCH-L1) gene, resulting in Ile93Met substitution in its gene product (UCH-L1 Ile93Met ). PARK5 is inherited in an autosomal-dominant mode, but whether the Ile93Met mutation gives rise to a gain-of-toxic-function or lossof-function of UCH-L1 protein remains controversial. Here, we investigated the selective vulnerabilities of dopaminergic (DA) neurons in UCH-L1-transgenic (Tg) and spontaneous UCH-L1-null gracile axonal dystrophy mice to an important PDcausing insult, abnormal accumulation of a-synuclein (aSyn).Immunohistochemistry of midbrain sections of a patient with sporadic PD showed aSyn-and UCH-L1-double-positive Lewy bodies in nigral DA neurons, suggesting physical and/or functional interaction between the two proteins in human PD brain. Recombinant adeno-associated viral vector-mediated over-expression of aSyn for 4 weeks significantly enhanced the loss of nigral DA cell bodies in UCH-L1
Ile93Met-Tg mice, but had weak effects in age-matched UCH-L1wild-type -Tg mice and non-Tg littermates. In contrast, the extent of aSyn-induced DA cell loss in gracile axonal dystrophy mice was not significantly different from wild-type littermates at 13-weeks post-injection. Our results support the hypothesis that PARK5 is caused by a gain-of-toxic-function of UCH-L1 Ile93Met mutant, and suggest that regulation of UCH-L1 in nigral DA cells could be a future target for treatment of PD. Keywords: a-synuclein, adeno-associated virus, dopaminergic neurons, Parkinson's disease, ubiquitin carboxyterminal hydrolase-L1. missense mutations resulting in amino acid substitutions in aSyn protein (Ala53Thr, Ala30Pro, or Glu46Lys) (Polymeropoulos et al. 1997;Kruger et al. 1998;Zarranz et al. 2004). Furthermore, PARK4 is caused by duplication or triplication of aSyn gene (SNCA) locus (Singleton et al. 2003;Nishioka et al. 2006). In sporadic cases of PD, aSyn protein is the major component of Lewy bodies (Spillantini et al. 1997;Baba et al. 1998). These findings suggest an important role for aSyn protein accumulation in DA cells in the pathogenesis of PD. Previous studies also reported that overexpression of aSyn protein by using a recombinant adeno-associated viral (rAAV) or lentiviral vector caused DA neurodegeneration in rats and monkeys (Kirik et al. 2002(Kirik et al. , 2003Lo Bianco et al. 2002;Yamada et al. 2004;Yasuda et al. 2007). Ubiquitin carboxy-terminal hydrolase-L1 constitutes 1-2% of brain proteins and functions in the ubiquitin-proteasome system (Wilkinson et al. 1989;Larsen et al. 1996Larsen et al. , 1998. The ubiquitin hydrolase activity of UCH-L1 is important to free reusable ubiquitin monomers. UCH-L1 protein is also known to bind to and stabilize monomeric ubiquitin molecule (Osaka et al. 2003). PARK5 is caused by a missense mutation in UCH-L1 gene resulting in Ile93Met substitution in UCH-L1 protein (UCH-L1 Ile93Met ), and inherited in an autosomal-dominant mode (Leroy et al...