Journal article
Structure-function analysis of the GlyR α2 subunit autism mutation p.R323L reveals a gain-of-function
Frontiers in Molecular Neuroscience, Vol.10, 158
2017
Abstract
Glycine receptors (GlyRs) containing the α2 subunit regulate cortical interneuron migration. Disruption of the GlyR α2 subunit gene (Glra2) in mice leads to disrupted dorsal cortical progenitor homeostasis, leading to a depletion of projection neurons and moderate microcephaly in newborn mice. In humans, rare variants in GLRA2, which is located on the X chromosome, are associated with autism spectrum disorder (ASD) in the hemizygous state in males. These include a microdeletion (GLRA2∆ex8-9) and missense mutations in GLRA2 (p.N109S and p.R126Q) that impair cell-surface expression of GlyR α2, and either abolish or markedly reduce sensitivity to glycine. We report the functional characterization of a third missense variant in GLRA2 (p.R323L), associated with autism, macrocephaly, epilepsy and hypothyroidism in a female proband. Using heterosynapse and macroscopic current recording techniques, we reveal that GlyR α2R323L exhibits reduced glycine sensitivity, but significantly increased inhibitory postsynaptic current (IPSC) rise and decay times. Site-directed mutagenesis revealed that the nature of the amino acid switch at position 323 is critical for impairment of GlyR function. Single-channel recordings revealed that the conductance of α2R323L β channels was higher than α2β channels. Longer mean opening durations induced by p.R323L may be due to a change in the gating pathway that enhances the stability of the GlyR open state. The slower synaptic decay times, longer duration active periods and increase in conductance demonstrates that the GlyR α2 p.R323L mutation results in an overall gain of function, and that GlyR α2 mutations can be pathogenic in the heterozygous state in females. © 2017 Zhang, Ho, Harvey, Lynch and Keramidas.
Details
- Title
- Structure-function analysis of the GlyR α2 subunit autism mutation p.R323L reveals a gain-of-function
- Authors
- Y Zhang (Author) - University of QueenslandT N T Ho (Author) - University of QueenslandRobert J Harvey (Author) - University College London, United KingdomJ W Lynch (Author) - University of QueenslandA Keramidas (Author) - University of Queensland
- Publication details
- Frontiers in Molecular Neuroscience, Vol.10, 158; 13
- Publisher
- Frontiers Research Foundation
- Date published
- 2017
- DOI
- 10.3389/fnmol.2017.00158
- ISSN
- 1662-5099
- Copyright note
- Copyright © 2017 Zhang, Ho, Harvey, Lynch and Keramidas. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
- Organisation Unit
- School of Health; University of the Sunshine Coast, Queensland; School of Health and Sport Sciences - Legacy; Centre for Bioinnovation; School of Health and Behavioural Sciences - Legacy
- Language
- English
- Record Identifier
- 99450457502621
- Output Type
- Journal article
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