The Ducky Mutation in Cacna2d2 Results in Altered Purkinje Cell Morphology and Is Associated with the Expression of a Truncated α2δ-2 Protein with Abnormal Function

• Published in: The Journal of biological chemistry Vol. 277; no. 10; p. 7684
• Main Authors: Jens Brodbeck, Anthony Davies, Jo-Maree Courtney, Alon Meir, Nuria Balaguero, Carles Canti, Fraser J. Moss, Karen M. Page, Wendy S. Pratt, Steven P. Hunt, Jane Barclay, Michele Rees, Annette C. Dolphin
• Format: Journal Article
• Language: English
• Published: American Society for Biochemistry and Molecular Biology 08.03.2002
• ISSN: 0021-9258; 1083-351X
• DOI: 10.1074/jbc.M109404200

The mouse mutant ducky, a model for absence epilepsy, is characterized by spike-wave seizures and cerebellar ataxia. A mutation in Cacna2d2 , the gene encoding the α2δ-2 voltage-dependent calcium channel accessory subunit, has been found to underlie the ducky phenotype. The α2δ-2 mRNA is strongly expressed in cerebellar Purkinje cells. We show that du/du mice have abnormalities in their Purkinje cell dendritic tree. The mutation in α2δ-2 results in the introduction of a premature stop codon and predicts the expression of a truncated protein encoded by the first three exons of Cacna2d2 , followed by 8 novel amino acids. We show that both mRNA and protein corresponding to this predicted transcript are expressed in du/du cerebellum and present in Purkinje cells. Whereas the α2δ-2 subunit increased the peak current density of the Ca V 2.1/β 4 channel combination when co-expressed in vitro , co-expression with the truncated mutant α2δ-2 protein reduced current density, indicating that it may contribute to the du phenotype.