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The Gdap1 knockout mouse mechanistically links redox control to Charcot-Marie-Tooth disease

Authors :
Niemann, Axel
Huber, Nina
Wagner, Konstanze M.
Somandin, Christian
Horn, Michael
Lebrun-Julien, Frédéric
Angst, Brigitte
Pereira, Jorge A.
Halfter, Hartmut
Welzl, Hans
Feltri, M. Laura
Wrabetz, Lawrence
Young, Peter
Wessig, Carsten
Toyka, Klaus V.
Suter, Ueli
Niemann, Axel
Huber, Nina
Wagner, Konstanze M.
Somandin, Christian
Horn, Michael
Lebrun-Julien, Frédéric
Angst, Brigitte
Pereira, Jorge A.
Halfter, Hartmut
Welzl, Hans
Feltri, M. Laura
Wrabetz, Lawrence
Young, Peter
Wessig, Carsten
Toyka, Klaus V.
Suter, Ueli
Publication Year :
2017

Abstract

Mutations in the mitochondrial fission factor GDAP1 are associated with severe peripheral neuropathies, but why the CNS remains unaffected is unclear. Using a Gdap1−/− mouse, Niemann et al. demonstrate that a CNS-expressed Gdap1 paralogue changes its subcellular localisation under oxidative stress conditions to also act as a mitochondrial fission factor

Details

Database :
OAIster
Notes :
English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1156691265
Document Type :
Electronic Resource