Synaptic dysfunction and abnormal behaviors in mice lacking major isoforms of Shank3.

Journal Article

SHANK3 is a synaptic scaffolding protein enriched in the postsynaptic density (PSD) of excitatory synapses. Small microdeletions and point mutations in SHANK3 have been identified in a small subgroup of individuals with autism spectrum disorder (ASD) and intellectual disability. SHANK3 also plays a key role in the chromosome 22q13.3 microdeletion syndrome (Phelan-McDermid syndrome), which includes ASD and cognitive dysfunction as major clinical features. To evaluate the role of Shank3 in vivo, we disrupted major isoforms of the gene in mice by deleting exons 4-9. Isoform-specific Shank3(e4-9) homozygous mutant mice display abnormal social behaviors, communication patterns, repetitive behaviors and learning and memory. Shank3(e4-9) male mice display more severe impairments than females in motor coordination. Shank3(e4-9) mice have reduced levels of Homer1b/c, GKAP and GluA1 at the PSD, and show attenuated activity-dependent redistribution of GluA1-containing AMPA receptors. Subtle morphological alterations in dendritic spines are also observed. Although synaptic transmission is normal in CA1 hippocampus, long-term potentiation is deficient in Shank3(e4-9) mice. We conclude that loss of major Shank3 species produces biochemical, cellular and morphological changes, leading to behavioral abnormalities in mice that bear similarities to human ASD patients with SHANK3 mutations.

Full Text

Duke Authors

Cited Authors

  • Wang, X; McCoy, PA; Rodriguiz, RM; Pan, Y; Je, HS; Roberts, AC; Kim, CJ; Berrios, J; Colvin, JS; Bousquet-Moore, D; Lorenzo, I; Wu, G; Weinberg, RJ; Ehlers, MD; Philpot, BD; Beaudet, AL; Wetsel, WC; Jiang, Y-H

Published Date

  • August 1, 2011

Published In

Volume / Issue

  • 20 / 15

Start / End Page

  • 3093 - 3108

PubMed ID

  • 21558424

Electronic International Standard Serial Number (EISSN)

  • 1460-2083

Digital Object Identifier (DOI)

  • 10.1093/hmg/ddr212

Language

  • eng

Conference Location

  • England