Article
ALS-linked P56S-VAPB, an aggregated loss-of-function mutant of VAPB, predisposes motor neurons to ER stress-related death by inducing aggregation of co-expressed wild-type VAPB.
Journal of neurochemistry - 1 Feb 2009
Suzuki Hiroaki, Kanekura Kohsuke, Levine Timothy P, Kohno Kenji, Olkkonen Vesa M, Aiso Sadakazu, Matsuoka Masaaki
Abstract excerpt
A point mutation (P56S) in the vapb gene encoding an endoplasmic reticulum (ER)-integrated membrane protein [vesicle-associated membrane protein-associated protein B (VAPB)] causes autosomal-dominant amyotrophic lateral sclerosis. In our earlier study, we showed that VAPB may be involved in the IRE1/XBP1 signaling of the unfolded protein response, an ER reaction to inhibit accumulation of unfolded/ misfolded...
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.
