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Missense mutation of Fmr1 results in impaired AMPAR-mediated plasticity and socio-cognitive deficits in mice.

Marta Prieto | Alessandra Folci | Gwénola Poupon | Sara Schiavi | Valeria Buzzelli | Marie Pronot | Urielle François | Paula Pousinha | Norma Lattuada | Sophie Abelanet | Sara Castagnola | Magda Chafai | Anouar Khayachi | Carole Gwizdek | Frédéric Brau | Emmanuel Deval | Maura Francolini | Barbara Bardoni | Yann Humeau | Viviana Trezza | Stéphane Martin
Nature communications | 2021

Fragile X syndrome (FXS) is the most frequent form of inherited intellectual disability and the best-described monogenic cause of autism. CGG-repeat expansion in the FMR1 gene leads to FMR1 silencing, loss-of-expression of the Fragile X Mental Retardation Protein (FMRP), and is a common cause of FXS. Missense mutations in the FMR1 gene were also identified in FXS patients, including the recurrent FMRP-R138Q mutation. To investigate the mechanisms underlying FXS caused by this mutation, we generated a knock-in mouse model (Fmr1R138Q) expressing the FMRP-R138Q protein. We demonstrate that, in the hippocampus of the Fmr1R138Q mice, neurons show an increased spine density associated with synaptic ultrastructural defects and increased AMPA receptor-surface expression. Combining biochemical assays, high-resolution imaging, electrophysiological recordings, and behavioural testing, we also show that the R138Q mutation results in impaired hippocampal long-term potentiation and socio-cognitive deficits in mice. These findings reveal the functional impact of the FMRP-R138Q mutation in a mouse model of FXS.

Pubmed ID: 33692361

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Fiji (tool)

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