Mutations in the gene encoding cystatin B in progressive myoclonus epilepsy (EPM1)

Abstract

Progressive myoclonus epilepsy of the Unverricht-Lundborg type (EPM1) is an autosomal recessive inherited form of epilepsy, previously linked to human chromosome 21q22.3. The gene coding cystatin B was shown to be localized to this region, and levels of messenger RNA encoded by this region were found to be decreased in the cells from affected individuals. Two mutations, a 3' splice site mutation and a stop codon mutation, were identified in the gene encoding cystatin B in EPM1 patient but were not present in unaffected individuals. These results provide evidence that mutations in the gene encoding cystatin B are responsible for the primary defect in patients with EPM1.