Science · 2011 · 169 citations · 14 references
Life SciencesGeneticsMolecular GeneticsMolecular NeuroscienceNeurodegenerationNeurogeneticsExercise InterventionsExercise TherapyMolecular Basis Of NeurodegenerationNeurodegenerative DiseasesNeurodegenerative DisordersSpinocerebellar AtaxiasGain Of Toxic FunctionHereditary AtaxiasNeurodegenerative Disease MechanismsPolyglutamine Expansion DisordersRescueSpinocerebellar Ataxia GeneticsSpinocerebellar Ataxia ModelsSpinocerebellar Ataxia Type 1
Spinocerebellar ataxia type 1 (SCA1) is a fatal neurodegenerative disease caused by expansion of a translated CAG repeat in Ataxin-1 (ATXN1). To determine the long-term effects of exercise, we implemented a mild exercise regimen in a mouse model of SCA1 and found a considerable improvement in survival accompanied by up-regulation of epidermal growth factor and consequential down-regulation of Capicua, which is an ATXN1 interactor. Offspring of Capicua mutant mice bred to SCA1 mice showed significant improvement of all disease phenotypes. Although polyglutamine-expanded Atxn1 caused some loss of Capicua function, further reduction of Capicua levels--either genetically or by exercise--mitigated the disease phenotypes by dampening the toxic gain of function. Thus, exercise might have long-term beneficial effects in other ataxias and neurodegenerative diseases.
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Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1
Harry T. Orr, Ming‐Yi Chung, Sandro Banfi et al. · Nature Genetics · 1993 · 1.7K citations
Intensive coordinative training improves motor performance in degenerative cerebellar disease
Winfried Ilg, Matthis Synofzik, Doris Brötz et al. · Neurology · 2009 · 333 citations · Full text