Rare GABRA3 variants are associated with epileptic seizures, encephalopathy and dysmorphic features.

Niturad CE¹, Lev D^2,3,4, Kalscheuer VM^5,6, Charzewska A⁷, Schubert J^1,8, Lerman-Sagie T^3,4,9, Kroes HY¹⁰, Oegema R¹⁰, Traverso M¹¹, Specchio N¹², Lassota M¹³, Chelly J¹⁴, Bennett-Back O¹⁵, Carmi N^3,4,10, Koffler-Brill T¹⁶, Iacomino M¹¹, Trivisano M¹², Capovilla G¹⁷, Striano P¹⁸, Nawara M⁷, Rzonca S⁷, Fischer U^5,6, Bienek M⁵, Jensen C⁵, Hu H⁵, Thiele H¹⁹, Altmüller J^19,20, Krause R⁸, May P⁸, Becker F¹; EuroEPINOMICS Consortium, Balling R⁸, Biskup S²¹, Haas SA²², Nürnberg P¹⁹, van Gassen KLI¹⁰, Lerche H¹, Zara F¹¹, Maljevic S¹, Leshinsky-Silver E^2,3,16

Genetic epilepsies are caused by mutations in a range of different genes, many of them encoding ion channels, receptors or transporters. While the number of detected variants and genes increased dramatically in the recent years, pleiotropic effects have also been recognized, revealing that clinical syndromes with various degrees of severity arise from a single gene, a single mutation, or from different mutations showing similar functional defects. Accordingly, several genes coding for GABAA receptor subunits have been linked to a spectrum of benign to severe epileptic disorders and it was shown that a loss of function presents the major correlated pathomechanism. Here, we identified six variants in GABRA3 encoding the α3-subunit of the GABAA receptor. This gene is located on chromosome Xq28 and has not been previously associated with human disease. Five missense variants and one microduplication were detected in four families and two sporadic cases presenting with a range of epileptic seizure types, a varying degree of intellectual disability and developmental delay, sometimes with dysmorphic features or nystagmus. The variants co-segregated mostly but not completely with the phenotype in the families, indicating in some cases incomplete penetrance, involvement of other genes, or presence of phenocopies. Overall, males were more severely affected and there were three asymptomatic female mutation carriers compared to only one male without a clinical phenotype. X-chromosome inactivation studies could not explain the phenotypic variability in females. Three detected missense variants are localized in the extracellular GABA-binding NH2-terminus, one in the M2-M3 linker and one in the M4 transmembrane segment of the α3-subunit. Functional studies in Xenopus laevis oocytes revealed a variable but significant reduction of GABA-evoked anion currents for all mutants compared to wild-type receptors. The degree of current reduction correlated partially with the phenotype. The microduplication disrupted GABRA3 expression in fibroblasts of the affected patient. In summary, our results reveal that rare loss-of-function variants in GABRA3 increase the risk for a varying combination of epilepsy, intellectual disability/developmental delay and dysmorphic features, presenting in some pedigrees with an X-linked inheritance pattern.