Epilepsy-associated SCN2A (NaV1.2) variants exhibit diverse and complex functional properties

Christopher Hal Thompson, Franck Potet, Tatiana V. Abramova, Jean Marc DeKeyser, Nora F. Ghabra, Carlos G. Vanoye, John J Millichap, Alfred Lewis George

Research output: Contribution to journalArticlepeer-review

3 Scopus citations


Pathogenic variants in voltage-gated sodium (NaV) channel genes including SCN2A,encodingNaV1.2, are discovered frequently in neurodevelopmental disorders with or without epilepsy. SCN2A is also a high-confidence risk gene for autism spectrum disorder (ASD) and nonsyndromic intellectual disability (ID). Previous work to determine the functional consequences of SCN2A variants yielded a paradigm in which predominantly gain-of-function variants cause neonatal-onset epilepsy, whereas loss-of-function variants are associated with ASD and ID. However, this framework was derived from a limited number of studies conducted under heterogeneous experimental conditions, whereas most disease-associated SCN2A variants have not been functionally annotated. We determined the functional properties of SCN2A variants using automated patch-clamp recording to demonstrate the validity of this method and to examine whether a binary classification of variant dysfunction is evident in a larger cohort studied under uniform conditions. We studied 28 disease-associated variants and 4 common variants using two alternatively spliced isoforms of NaV1.2 expressed in HEK293T cells. Automated patch-clamp recording provided a valid high throughput method to ascertain detailed functional properties of NaV1.2 variants with concordant findings for variants that were previously studied using manual patch clamp. Many epilepsy-associated variants in our study exhibited complex patterns of gain-and loss-of-functions that are difficult to classify by a simple binary scheme. The higher throughput achievable with automated patch clamp enables study of variants with greater standardization of recording conditions, freedom from operator bias, and enhanced experimental rigor. This approach offers an enhanced ability to discern relationships between channel dysfunction and neurodevelopmental disorders.

Original languageEnglish (US)
Article numbere202313375
JournalJournal of General Physiology
Issue number10
StatePublished - Oct 2 2023

ASJC Scopus subject areas

  • Physiology


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