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          Institute: MPI für Informatik     Collection: Computational Biology and Applied Algorithmics     Display Documents



ID: 314637.0, MPI für Informatik / Computational Biology and Applied Algorithmics
An arginine/lysine-rich motif is crucial for VCP/p97-mediated modulation of ataxin-3 fibrillogenesis
Authors:Boeddrich, Annett; Gaumer, Sébastien; Haacke, Annette; Tzvetkov, Nikolay; Albrecht, Mario; Evert, Bernd O.; Müller, Eva C.; Lurz, Rudi; Breuer, Peter; Schugardt, Nancy; Plaßmann, Stephanie; Xu, Kexiang; Warrick, John M.; Suopanki, Jaana; Wüllner, Ullrich; Frank, Ronald; Hartl, Ulrich F.; Bonini, Nancy M.; Wanker, Erich E.
Language:English
Date of Publication (YYYY-MM-DD):2006
Title of Journal:EMBO Journal
Volume:25
Start Page:1547
End Page:1558
Review Status:Peer-review
Audience:Experts Only
Intended Educational Use:No
Abstract / Description:Arginine/lysine-rich motifs typically function as targeting signals for the
translocation of proteins to the nucleus. Here, we demonstrate that such a
motif consisting of four basic amino acids in the polyglutamine protein
ataxin-3 (Atx-3) serves as a recognition site for the interaction with the
molecular chaperone VCP. Through this interaction, VCP modulates the
fibrillogenesis of pathogenic forms of Atx-3 in a concentration-dependent
manner, with low concentrations of VCP stimulating fibrillogenesis and excess
concentrations suppressing it. No such effect was observed with a mutant Atx-3
variant, which does not contain a functional VCP interaction motif. Strikingly,
a stretch of four basic amino acids in the ubiquitin chain assembly factor E4B
was also discovered to be critical for VCP binding, indicating that
arginine/lysine-rich motifs might be generally utilized by VCP for the
targeting of proteins. In vivo studies with Drosophila models confirmed that
VCP selectively modulates aggregation and neurotoxicity induced by pathogenic
Atx-3. Together, these results define the VCP–Atx-3 association as a potential
target for therapeutic intervention and suggest that it might influence the
progression of spinocerebellar ataxia type 3.
Last Change of the Resource (YYYY-MM-DD):2007-02-20
External Publication Status:published
Document Type:Article
Communicated by:Thomas Lengauer
Affiliations:MPI für Informatik/Computational Biology and Applied Algorithmics
Identifiers:LOCALID:C125673F004B2D7B-4ED11F9CF875526CC125713A0067DB36-...
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