科研之友
微信
新浪微博
Facebook
分享链接
摘要
Objective: Autosomal dominant cortical myoclonus and epilepsy (ADCME) is characterized by distal, fairly rhythmic myoclonus and epilepsy with variable severity. We have previously mapped the disease locus on chromosome 2p11.1-q12.2 by genome-wide linkage analysis. Additional pedigrees affected by similar forms of epilepsy have been associated with chromosomes 8q, 5p, and 3q, but none of the causing genes has been identified. We aim to identify the mutant gene responsible for this form of epilepsy. %26lt;br%26gt;Methods: Genes included in the ADCME critical region were directly sequenced. Coimmunoprecipitation, immunofluorescent, and electrophysiologic approaches to transfected human cells have been utilized for testing the functional significance of the identified mutation. %26lt;br%26gt;Results: Here we show that mutation in the alpha(2)-adrenergic receptor subtype B (alpha(2B)-AR) is associated with ADCME by identifying a novel in-frame insertion/deletion in 2 Italian families. The mutation alters several conserved residues of the third intracellular loop, hampering neither the alpha(2B)-AR plasma membrane localization nor the arrestin-mediated internalization capacity, but altering the binding with the scaffolding protein spinophilin upon neurotransmitter activation. Spinophilin, in turn, regulates interaction of G protein coupled receptors with regulator of G protein signaling proteins. Accordingly, the mutant alpha(2B)-AR increases the epinephrine-stimulated calcium signaling. %26lt;br%26gt;Interpretation: The identified mutation is responsible for ADCME, as the loss of alpha(2B)-AR/spinophilin interaction causes a gain of function effect. This work implicates for the first time the alpha-adrenergic system in human epilepsy and opens new ways of understanding the molecular pathway of epileptogenesis, widening the spectrum of possible therapeutic targets.
- 出版日期2014-1
- 单位NIH
