Genetic and functional analyses demonstrate a role for abnormal glycinergic signaling in autism

M. Pilorge, C. Fassier, H. Le Corronc, A. Potey, J. Bai, S. De Gois, E. Delaby, B. Assouline, V. Guinchat, F. Devillard, R. Delorme, G. Nygren, M. Rastam, J. C. Meier, S. Otani, H. Cheval, V. M. James, M. Topf, T. N. Dear, C. GillbergM. Leboyer, B. Giros, S. Gautron, J. Hazan, R. J. Harvey, P. Legendre, C. Betancur

Research output: Contribution to journalArticlepeer-review

47 Citations (Scopus)

Abstract

Autism spectrum disorder (ASD) is a common neurodevelopmental condition characterized by marked genetic heterogeneity. Recent studies of rare structural and sequence variants have identified hundreds of loci involved in ASD, but our knowledge of the overall genetic architecture and the underlying pathophysiological mechanisms remains incomplete. Glycine receptors (GlyRs) are ligand-gated chloride channels that mediate inhibitory neurotransmission in the adult nervous system but exert an excitatory action in immature neurons. GlyRs containing the α;2 subunit are highly expressed in the embryonic brain, where they promote cortical interneuron migration and the generation of excitatory projection neurons. We previously identified a rare microdeletion of the X-linked gene GLRA2, encoding the GlyR α;2 subunit, in a boy with autism. The microdeletion removes the terminal exons of the gene (GLRA2 Δex8-9). Here, we sequenced 400 males with ASD and identified one de novo missense mutation, p.R153Q, absent from controls. In vitro functional analysis demonstrated that the GLRA2 Δex8 - 9 protein failed to localize to the cell membrane, while the R153Q mutation impaired surface expression and markedly reduced sensitivity to glycine. Very recently, an additional de novo missense mutation (p.N136S) was reported in a boy with ASD, and we show that this mutation also reduced cell-surface expression and glycine sensitivity. Targeted glra2 knockdown in zebrafish induced severe axon-branching defects, rescued by injection of wild type but not GLRA2 Δex8-9 or R153Q transcripts, providing further evidence for their loss-of-function effect. Glra2 knockout mice exhibited deficits in object recognition memory and impaired long-term potentiation in the prefrontal cortex. Taken together, these results implicate GLRA2 in non-syndromic ASD, unveil a novel role for GLRA2 in synaptic plasticity and learning and memory, and link altered glycinergic signaling to social and cognitive impairments.

Original languageEnglish
Pages (from-to)936-945
Number of pages10
JournalMolecular psychiatry
Volume21
Issue number7
DOIs
Publication statusPublished or Issued - 1 Jul 2016

ASJC Scopus subject areas

  • Molecular Biology
  • Psychiatry and Mental health
  • Cellular and Molecular Neuroscience

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