TY - JOUR T1 - Normal CA1 place fields but discoordinated network discharge in a Fmr1-null mouse model of fragile X syndrome JF - bioRxiv DO - 10.1101/152462 SP - 152462 AU - Fraser Todd Sparks AU - Zoe Nicole Talbot AU - Dino Dvorak AU - Bridget Mary Curran AU - Juan Marcos Alarcon AU - André Antonio Fenton Y1 - 2017/01/01 UR - http://biorxiv.org/content/early/2017/06/20/152462.abstract N2 - Silence of FMR1 causes loss of fragile X mental retardation protein (FMRP) and dysregulated translation at synapses, resulting in the intellectual disability and autistic symptoms of Fragile X Syndrome (FXS). Synaptic dysfunction hypotheses for how intellectual disabilities like cognitive inflexibility arise in FXS, predict impaired neural coding in the absence of FMRP. We tested the prediction by comparing hippocampus place cells in wild-type and FXS-model mice. Experience-driven CA1 synaptic function and synaptic plasticity changes are excessive in Fmr1-null mice, but CA1 place fields are normal. However, Fmr1-null discharge relationships to local field potential oscillations are abnormally weak, stereotyped, and homogeneous; also discharge coordination within Fmr1-null place cell networks is weaker and less reliable than wild-type. Rather than disruption of single-cell neural codes, these findings point to invariant tuning of single-cell responses and inadequate discharge coordination within neural ensembles as a pathophysiological basis of cognitive inflexibility in FXS. ER -