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Hot-spot residue in small heat-shock protein 22 causes distal motor neuropathy
Authors:Irobi Joy  Van Impe Katrien  Seeman Pavel  Jordanova Albena  Dierick Ines  Verpoorten Nathalie  Michalik Andrej  De Vriendt Els  Jacobs An  Van Gerwen Veerle  Vennekens Krist'l  Mazanec Radim  Tournev Ivailo  Hilton-Jones David  Talbot Kevin  Kremensky Ivo  Van Den Bosch Ludo  Robberecht Wim  Van Vandekerckhove Joël  Van Broeckhoven Christine  Gettemans Jan  De Jonghe Peter  Timmerman Vincent
Institution:Department of Molecular Genetics, Flanders Interuniversity Institute for Biotechnology, University of Antwerp, Universiteitsplein 1, B-2610 Antwerpen, Belgium.
Abstract:Distal hereditary motor neuropathies are pure motor disorders of the peripheral nervous system resulting in severe atrophy and wasting of distal limb muscles. In two pedigrees with distal hereditary motor neuropathy type II linked to chromosome 12q24.3, we identified the same mutation (K141N) in small heat-shock 22-kDa protein 8 (encoded by HSPB8; also called HSP22). We found a second mutation (K141E) in two smaller families. Both mutations target the same amino acid, which is essential to the structural and functional integrity of the small heat-shock protein alphaA-crystallin. This positively charged residue, when mutated in other small heat-shock proteins, results in various human disorders. Coimmunoprecipitation experiments showed greater binding of both HSPB8 mutants to the interacting partner HSPB1. Expression of mutant HSPB8 in cultured cells promoted formation of intracellular aggregates. Our findings provide further evidence that mutations in heat-shock proteins have an important role in neurodegenerative disorders.
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