A novel de novo KCNB1variant altering channel characteristics in a patient with periventricular heterotopia, abnormal corpus callosum, and mild seizure outcome

Autor: Hiraide, Takuya, Akita, Tenpei, Uematsu, Kenji, Miyamoto, Sachiko, Nakashima, Mitsuko, Sasaki, Masayuki, Fukuda, Atsuo, Kato, Mitsuhiro, Saitsu, Hirotomo
Zdroj: Journal of Human Genetics; 20220101, Issue: Preprints p1-7, 7p
Abstrakt: KCNB1encodes the α-subunit of Kv2.1, the main contributor to neuronal delayed rectifier potassium currents. The subunit consists of six transmembrane α helices (S1–S6), comprising the voltage-sensing domain (S1–S4) and the pore domain (S5-P-S6). Heterozygous KCNB1pathogenic variants are associated with developmental and epileptic encephalopathy. Here we report an individual who shows the milder phenotype compared to the previously reported cases, including delayed language development, mild intellectual disability, attention deficit hyperactivity disorder, late-onset epilepsy responsive to an antiepileptic drug, elevation of serum creatine kinase, and peripheral axonal neuropathy. On the other hand, his brain MRI showed characteristic findings including periventricular heterotopia, polymicrogyria, and abnormal corpus callosum. Exome sequencing identified a novel de novo KCNB1variant c.574G>A, p.(Ala192Thr) located in the S1 segment of the voltage-sensing domain. Functional analysis using the whole-cell patch-clamp technique in Neuro2a cells showed that the Ala192Thr mutant reduces both activation and inactivation of the channel at membrane voltages in the range of −50 to −30 mV. Our case could expand the phenotypic spectrum of patients with KCNB1variants, and suggested that variants located in the S1 segment might be associated with a milder outcome of seizures.
Databáze: Supplemental Index
Externí odkaz: