4.8 Article

Yeast Reveal a Druggable Rsp5/Nedd4 Network that Ameliorates α-Synuclein Toxicity in Neurons

Journal

SCIENCE
Volume 342, Issue 6161, Pages 979-983

Publisher

AMER ASSOC ADVANCEMENT SCIENCE
DOI: 10.1126/science.1245321

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Funding

  1. NIH [5R01GM069530, GM58160]
  2. National Research Service Award (NRSA) fellowship [F32NS061419, F32GM099817]
  3. JPB Foundation
  4. Eleanor Schwartz Charitable Foundation
  5. HHMI
  6. Bachmann-Strauss Dystonia & Parkinson Foundation

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alpha-Synuclein (alpha-syn) is a small lipid-binding protein implicated in several neurodegenerative diseases, including Parkinson's disease, whose pathobiology is conserved from yeast to man. There are no therapies targeting these underlying cellular pathologies, or indeed those of any major neurodegenerative disease. Using unbiased phenotypic screens as an alternative to target-based approaches, we discovered an N-aryl benzimidazole (NAB) that strongly and selectively protected diverse cell types from alpha-syn toxicity. Three chemical genetic screens in wild-type yeast cells established that NAB promoted endosomal transport events dependent on the E3 ubiquitin ligase Rsp5/Nedd4. These same steps were perturbed by alpha-syn itself. Thus, NAB identifies a druggable node in the biology of alpha-syn that can correct multiple aspects of its underlying pathology, including dysfunctional endosomal and endoplasmic reticulum-to-Golgi vesicle trafficking.

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