APA
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Davakan, A., Cmarko, L., Oliveira-Mendes, B. R., Bernat, C., Boulali, N., Montnach, J., … Lory, P. (2025). Electrophysiological classification of CACNA1G gene variants associated with neurodevelopmental and neurological disorders. BioRxiv.
Chicago/Turabian
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Davakan, Amaël, Leos Cmarko, Barbara Ribeiro Oliveira-Mendes, Claire Bernat, Najlae Boulali, J. Montnach, Stephanie E. Vallee, et al. “Electrophysiological Classification of CACNA1G Gene Variants Associated with Neurodevelopmental and Neurological Disorders.” bioRxiv (2025).
MLA
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Davakan, Amaël, et al. “Electrophysiological Classification of CACNA1G Gene Variants Associated with Neurodevelopmental and Neurological Disorders.” BioRxiv, 2025.
BibTeX Click to copy
@article{ama2025a,
title = {Electrophysiological classification of CACNA1G gene variants associated with neurodevelopmental and neurological disorders},
year = {2025},
journal = {bioRxiv},
author = {Davakan, Amaël and Cmarko, Leos and Oliveira-Mendes, Barbara Ribeiro and Bernat, Claire and Boulali, Najlae and Montnach, J. and Vallee, Stephanie E. and Dinulos, M. and Burglen, L. and Cantagrel, Vincent and Weiss, Norbert and Nicole, Sophie and Monteil, Arnaud and Waard, M. De and Lory, Philippe}
}
This study highlights the complementarity of automated patch-clamp (APC) and manual patch-clamp (MPC) approaches to describe the electrophysiological properties of eighteen Cav3.1 calcium channel variants associated with various neurological conditions. Current density was measured efficiently for all variants in APC experiments, with four variants (p.V184G, p.N1200S, p.S1263A and p.D2242N) showing high current densities, compared to wild-type Cav3.1 channel, while six variants (p.M197R, p.V392M, p.F956del, p.I962N, p.I1412T, and p.G1534D) displayed low current densities, and were therefore preferentially studied using MPC. The electrophysiological properties were well conserved in APC (e.g. inactivation and deactivation kinetics, steady-state properties), with only the APC-MPC correlation for the activation kinetics being less robust. In addition, neuronal modeling, using a deep cerebellar neuron (DCN) environment, revealed that most of the variants localized in the intracellular gate (S5 and S6 segments) could increase DCN spike frequencies. This DCN firing was critically dependent on the current density and further pointed to the gain-of-function (GOF) properties of p.A961T and p.M1531V, the recurrent variants associated with Spinocerebellar Ataxia type-42 with Neurodevelopmental Deficit (SCA42ND). Action-potential (AP) clamp experiments performed using cerebellar and thalamic neuron activities further established the GOF properties of p.A961T and p.M1531V variants. Overall, this study demonstrates that APC is well-suited to high-throughput analysis of Cav3.1 channel variants, and that MPC complements APC for characterizing low-expression variants. Furthermore, in silico modeling and AP clamp experiments establish that the gain- or loss-of-function properties of the variants are determined by how the Cav3.1 channel decodes the electrophysiological context of a neuron.