Dataset Information

Functional Investigation of a GRIN2A Variant Associated with Rolandic Epilepsy.

ABSTRACT: N-methyl-D-aspartate receptors (NMDARs), a subtype of glutamate-gated ion channels, play a central role in epileptogenesis. Recent studies have identified an increasing number of GRIN2A (a gene encoding the NMDAR GluN2A subunit) mutations in patients with epilepsy. Phenotypes of GRIN2A mutations include epilepsy-aphasia disorders and other epileptic encephalopathies, which pose challenges in clinical treatment. Here we identified a heterozygous GRIN2A mutation (c.1341T>A, p.N447K) from a boy with Rolandic epilepsy by whole-exome sequencing. The patient became seizure-free with a combination of valproate and lamotrigine. Functional investigation was carried out using recombinant NMDARs containing a GluN2A-N447K mutant that is located in the ligand-binding domain of the GluN2A subunit. Whole-cell current recordings in HEK 293T cells revealed that the N447K mutation increased the NMDAR current density by ~1.2-fold, enhanced the glutamate potency by 2-fold, and reduced the sensitivity to Mg2+ inhibition. These results indicated that N447K is a gain-of-function mutation. Interestingly, alternative substitutions by alanine and glutamic acid at the same residue (N447A and N447E) did not change NMDAR function, suggesting a residual dependence of this mutation in altering NMDAR function. Taken together, this study identified human GluN2A N447K as a novel mutation associated with epilepsy and validated its functional consequences in vitro. Identification of this mutation is also helpful for advancing our understanding of the role of NMDARs in epilepsy and provides new insights for precision therapeutics in epilepsy.

SUBMITTER: Xu XX

PROVIDER: S-EPMC5856713 | biostudies-literature | 2018 Apr

REPOSITORIES: biostudies-literature

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Functional Investigation of a GRIN2A Variant Associated with Rolandic Epilepsy.

Xu Xing-Xing XX Liu Xiao-Rong XR Fan Cui-Ying CY Lai Jin-Xing JX Shi Yi-Wu YW Yang Wei W Su Tao T Xu Jun-Yu JY Luo Jian-Hong JH Liao Wei-Ping WP

Neuroscience bulletin 20170921 2

N-methyl-D-aspartate receptors (NMDARs), a subtype of glutamate-gated ion channels, play a central role in epileptogenesis. Recent studies have identified an increasing number of GRIN2A (a gene encoding the NMDAR GluN2A subunit) mutations in patients with epilepsy. Phenotypes of GRIN2A mutations include epilepsy-aphasia disorders and other epileptic encephalopathies, which pose challenges in clinical treatment. Here we identified a heterozygous GRIN2A mutation (c.1341T>A, p.N447K) from a boy wit ...[more]

PMID: 28936771

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Functional Investigation of a GRIN2A Variant Associated with Rolandic Epilepsy.

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Functional Investigation of a GRIN2A Variant Associated with Rolandic Epilepsy.

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