Presented By: Department of Molecular, Cellular, and Developmental Biology
Molecular Basis of Inherited Parkinson’s disease
Suzanne Pfeffer, Stanford University
Note: change in time to 1 PM
Abstract: Today more than 1 million people in the U.S. suffer from Parkinson’s disease, and although most cases are idiopathic,perhaps as many as 20% of cases have a genetic basis. We study the effect of mutations in the LRRK2 kinase that is the most frequent cause of inherited Parkinson’s. Pathogenic LRRK2 phosphorylates a subset of Rab GTPases that are
master regulators of membrane trafficking. We have discovered that Rab10 phosphorylation flips a switch on its function —phosphoRab10 bind an entirely new set of effectors that regulate the formation of primary cilia in cell culture and mouse brain. We are also studying regulation of LRRK2 by the PPM1H phosphatase and how loss of cilia could trigger Parkinson’s disease.
Host: Ming Li
Abstract: Today more than 1 million people in the U.S. suffer from Parkinson’s disease, and although most cases are idiopathic,perhaps as many as 20% of cases have a genetic basis. We study the effect of mutations in the LRRK2 kinase that is the most frequent cause of inherited Parkinson’s. Pathogenic LRRK2 phosphorylates a subset of Rab GTPases that are
master regulators of membrane trafficking. We have discovered that Rab10 phosphorylation flips a switch on its function —phosphoRab10 bind an entirely new set of effectors that regulate the formation of primary cilia in cell culture and mouse brain. We are also studying regulation of LRRK2 by the PPM1H phosphatase and how loss of cilia could trigger Parkinson’s disease.
Host: Ming Li
Co-Sponsored By
Livestream Information
ZoomApril 9, 2021 (Friday) 1:00pm
Meeting ID: 91720907625
Explore Similar Events
-
Loading Similar Events...
