α-Synuclein Blocks ER-Golgi Traffic and Rab1 Rescues Neuron Loss in Parkinson's Models
Howard Hughes Medical Institute · Whitehead Institute for Biomedical Research · +5 more institutions
Abstract
Alpha-synuclein (alphaSyn) misfolding is associated with several devastating neurodegenerative disorders, including Parkinson's disease (PD). In yeast cells and in neurons alphaSyn accumulation is cytotoxic, but little is known about its normal function or pathobiology. The earliest defect following alphaSyn expression in yeast was a block in endoplasmic reticulum (ER)-to-Golgi vesicular trafficking. In a genomewide screen, the largest class of toxicity modifiers were proteins functioning at this same step, including the Rab guanosine triphosphatase Ypt1p, which associated with cytoplasmic alphaSyn inclusions. Elevated expression of Rab1, the mammalian YPT1 homolog, protected against alphaSyn-induced…
Citation impact
- FWCI
- 50.65
- Percentile
- 100%
- References
- 33
Authors
19- AAAntony A. CooperCorresponding
Howard Hughes Medical Institute, Whitehead Institute for Biomedical Research, University of Missouri–Kansas City, University of Pennsylvania
- ADAaron D. GitlerCorresponding
Howard Hughes Medical Institute, Whitehead Institute for Biomedical Research, University of Missouri–Kansas City, University of Pennsylvania
- AGAnil G. CashikarCorresponding
Howard Hughes Medical Institute, Whitehead Institute for Biomedical Research, University of Missouri–Kansas City, University of Pennsylvania
- CMCole M. HaynesCorresponding
Howard Hughes Medical Institute, Whitehead Institute for Biomedical Research, University of Missouri–Kansas City, University of Pennsylvania
- KJKathryn J. HillCorresponding
Howard Hughes Medical Institute, Whitehead Institute for Biomedical Research, University of Missouri–Kansas City, University of Pennsylvania
Topics & keywords
- Golgi apparatus
- Endoplasmic reticulum
- Rab
- Cell biology
- Biology
- Unfolded protein response
- LRRK2
- Parkinson's disease