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Dlg5 regulates dendritic spine formation and synaptogenesis by controlling subcellular N-cadherin localization.

The Journal of neuroscience : the official journal of the Society for Neuroscience | 2014

Most excitatory synapses in the mammalian brain are formed on dendritic spines, and spine density has a profound impact on synaptic transmission, integration, and plasticity. Membrane-associated guanylate kinase (MAGUK) proteins are intracellular scaffolding proteins with well established roles in synapse function. However, whether MAGUK proteins are required for the formation of dendritic spines in vivo is unclear. We isolated a novel disc large-5 (Dlg5) allele in mice, Dlg5(LP), which harbors a missense mutation in the DLG5 SH3 domain, greatly attenuating its ability to interact with the DLG5 GUK domain. We show here that DLG5 is a MAGUK protein that regulates spine formation, synaptogenesis, and synaptic transmission in cortical neurons. DLG5 regulates synaptogenesis by enhancing the cell surface localization of N-cadherin, revealing a key molecular mechanism for regulating the subcellular localization of this cell adhesion molecule during synaptogenesis.

Pubmed ID: 25232112 RIS Download

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Associated grants

  • Agency: NCI NIH HHS, United States
    Id: P30 CA015704
  • Agency: NCI NIH HHS, United States
    Id: R01 CA131047
  • Agency: NINDS NIH HHS, United States
    Id: R01 NS036715
  • Agency: Howard Hughes Medical Institute, United States

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This is a list of tools and resources that we have found mentioned in this publication.


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