Abstract

Fragile X Syndrome is the most common inherited intellectual disability, and Fragile X Syndrome patients often exhibit motor and learning deficits. It was previously shown that the fmr1 knock-out mice, a common mouse model of Fragile X Syndrome, recapitulates this motor learning deficit and that the deficit is associated with altered plasticity of dendritic spines. Here, we investigated the motor learning-induced turnover, stabilization and clustering of dendritic spines in the fmr1 knock-out mouse using a single forelimb reaching task and in vivo multiphoton imaging. We report that fmr1 knock-out mice have deficits in motor learning-induced changes in dendritic spine turnover and new dendritic spine clustering, but not the motor learning-induced long-term stabilization of new dendritic spines. These results suggest that a failure to establish the proper synaptic connections in both number and location, but not the stabilization of the connections that are formed, contributes to the motor learning deficit seen in the fmr1 knock-out mouse.

Highlights

  • Fragile X Syndrome (FXS) is the most common inherited intellectual disability [1]

  • This leads to transcriptional level silencing and a complete lack of the FMR1 gene product, Fragile X Mental Retardation Protein (FMRP) [3]

  • We report that in addition to the previously described impairment in formation of new spines, fmr1 KO mice have a deficit in motor learning-induced new dendritic spine clustering, but no deficit in the specific stabilization of newly formed dendritic spines

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Summary

Introduction

In 95% of cases, FXS is caused by a trinucleotide repeat expansion in the 5’ untranslated region of the FMR1 gene [2] This leads to transcriptional level silencing and a complete lack of the FMR1 gene product, Fragile X Mental Retardation Protein (FMRP) [3]. Targeted deletion of exon 5 of the mouse fmr gene produces a KO mouse lacking in FMRP [13] This fmr KO mouse shows physical and behavioral characteristics observed in humans with FXS [14,15,16,17], including a mild motor learning deficit [18]. We report that in addition to the previously described impairment in formation of new spines, fmr KO mice have a deficit in motor learning-induced new dendritic spine clustering, but no deficit in the specific stabilization of newly formed dendritic spines

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