| Literature DB >> 26152728 |
Søs G Mathiassen1, Ida B Larsen1, Esben G Poulsen1, Christian T Madsen2, Elena Papaleo1, Kresten Lindorff-Larsen1, Birthe B Kragelund1, Michael L Nielsen2, Franziska Kriegenburg3, Rasmus Hartmann-Petersen4.
Abstract
A mutation, L166P, in the cytosolic protein, PARK7/DJ-1, causes protein misfolding and is linked to Parkinson disease. Here, we identify the fission yeast protein Sdj1 as the orthologue of DJ-1 and calculate by in silico saturation mutagenesis the effects of point mutants on its structural stability. We also map the degradation pathways for Sdj1-L169P, the fission yeast orthologue of the disease-causing DJ-1 L166P protein. Sdj1-L169P forms inclusions, which are enriched for the Hsp104 disaggregase. Hsp104 and Hsp70-type chaperones are required for efficient degradation of Sdj1-L169P. This also depends on the ribosome-associated E3 ligase Ltn1 and its co-factor Rqc1. Although Hsp104 is absolutely required for proteasomal degradation of Sdj1-L169P aggregates, the degradation of already aggregated Sdj1-L169P occurs independently of Ltn1 and Rqc1. Thus, our data point to soluble Sdj1-L169P being targeted early by Ltn1 and Rqc1. The fraction of Sdj1-L169P that escapes this first inspection then forms aggregates that are subsequently cleared via an Hsp104- and proteasome-dependent pathway.Entities:
Keywords: Parkinson disease; Parkinson disease (autosomal recessive, early onset) 7 (PARK7); chaperone; proteasome; proteostasis; ubiquitin
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Year: 2015 PMID: 26152728 PMCID: PMC4543670 DOI: 10.1074/jbc.M115.662312
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157