ABSTRACT
Copy-number variants of chromosome 16 region 16p11.2 are linked to neuropsychiatric disorders and are among the most prevalent in autism spectrum disorders. Of many 16p11.2 genes, Kctd13 has been implicated as a major driver of neurodevelopmental phenotypes. The function of KCTD13 in the mammalian brain, however, remains unknown. Here we delete the Kctd13 gene in mice and demonstrate reduced synaptic transmission. Reduced synaptic transmission correlates with increased levels of Ras homolog gene family, member A (RhoA), a KCTD13/CUL3 ubiquitin ligase substrate, and is reversed by RhoA inhibition, suggesting increased RhoA as an important mechanism. In contrast to a previous knockdown study, deletion of Kctd13 or kctd13 does not increase brain size or neurogenesis in mice or zebrafish, respectively. These findings implicate Kctd13 in the regulation of neuronal function relevant to neuropsychiatric disorders and clarify the role of Kctd13 in neurogenesis and brain size. Our data also reveal a potential role for RhoA as a therapeutic target in disorders associated with KCTD13 deletion.
Subject(s)
Brain/metabolism , Carrier Proteins/metabolism , Gene Deletion , Synaptic Transmission/genetics , Zebrafish Proteins/metabolism , rho GTP-Binding Proteins/metabolism , Animals , Autism Spectrum Disorder/genetics , Autism Spectrum Disorder/psychology , Autistic Disorder/genetics , Autistic Disorder/psychology , Brain/anatomy & histology , Brain/cytology , Brain/pathology , CA1 Region, Hippocampal/metabolism , CA1 Region, Hippocampal/pathology , Carrier Proteins/genetics , Chromosome Deletion , Chromosome Disorders/genetics , Chromosome Disorders/psychology , Chromosomes, Human, Pair 16/genetics , Cullin Proteins/metabolism , Female , Intellectual Disability/genetics , Intellectual Disability/psychology , Male , Mice , Multifactorial Inheritance/genetics , Neurogenesis/genetics , Organ Size/genetics , Reproducibility of Results , Synaptic Transmission/drug effects , Ubiquitin-Protein Ligase Complexes , Zebrafish , Zebrafish Proteins/genetics , rho GTP-Binding Proteins/antagonists & inhibitors , rhoA GTP-Binding ProteinABSTRACT
Mutations/deletions in the SHANK3 gene are associated with autism spectrum disorders and intellectual disability. Here, we present electrophysiological and behavioral consequences in novel heterozygous and homozygous mice with a transcriptional stop cassette inserted upstream of the PDZ domain-coding exons in Shank3 (Shank3E13 ). Insertion of a transcriptional stop cassette prior to exon 13 leads to loss of the two higher molecular weight isoforms of Shank3. Behaviorally, both Shank3E13 heterozygous (HET) and homozygous knockout (KO) mice display increased repetitive grooming, deficits in social interaction tasks, and decreased rearing. Shank3E13 KO mice also display deficits in spatial memory in the Morris water maze task. Baseline hippocampal synaptic transmission and short-term plasticity are preserved in Shank3E13 HET and KO mice, while both HET and KO mice exhibit impaired hippocampal long-term plasticity. Additionally, Shank3E13 HET and KO mice display impaired striatal glutamatergic synaptic transmission. These results demonstrate for the first time in this novel Shank3 mutant that both homozygous and heterozygous mutation of Shank3 lead to behavioral abnormalities with face validity for autism along with widespread synaptic dysfunction. Autism Res 2017, 10: 42-65. © 2016 International Society for Autism Research, Wiley Periodicals, Inc.
Subject(s)
Autistic Disorder/genetics , Autistic Disorder/physiopathology , Corpus Striatum/physiopathology , Hippocampus/physiopathology , Mutation/genetics , Nerve Tissue Proteins/genetics , Animals , Behavior, Animal , Blotting, Western , Disease Models, Animal , Exons , Female , Male , Mice , Mice, Knockout , Microfilament Proteins , Reproducibility of Results , Sequence Deletion , Synaptic Transmission/physiologyABSTRACT
The Reelin signaling pathway is implicated in processes controlling synaptic plasticity and hippocampus-dependent learning and memory. A single direct in vivo application of Reelin enhances long-term potentiation, increases dendritic spine density and improves associative and spatial learning and memory. Angelman syndrome (AS) is a neurological disorder that presents with an overall defect in synaptic function, including decreased long-term potentiation, reduced dendritic spine density, and deficits in learning and memory, making it an attractive model in which to examine the ability of Reelin to recover synaptic function and cognitive deficits. In this study, we investigated the effects of Reelin administration on synaptic plasticity and cognitive function in a mouse model of AS and demonstrated that bilateral, intraventricular injections of Reelin recover synaptic function and corresponding hippocampus-dependent associative and spatial learning and memory. Additionally, we describe alteration of the Reelin profile in tissue from both the AS mouse and post-mortem human brain.
Subject(s)
Angelman Syndrome/physiopathology , Angelman Syndrome/psychology , Cell Adhesion Molecules, Neuronal/administration & dosage , Extracellular Matrix Proteins/administration & dosage , Hippocampus/drug effects , Long-Term Potentiation/drug effects , Nerve Tissue Proteins/administration & dosage , Serine Endopeptidases/administration & dosage , Angelman Syndrome/drug therapy , Animals , Cell Adhesion Molecules, Neuronal/metabolism , Cerebral Cortex/metabolism , Dendritic Spines/drug effects , Disease Models, Animal , Extracellular Matrix Proteins/metabolism , Female , HEK293 Cells , Hippocampus/physiopathology , Hippocampus/ultrastructure , Humans , Injections, Intraventricular , Male , Mice , Motor Activity/drug effects , Nerve Tissue Proteins/metabolism , Reelin Protein , Serine Endopeptidases/metabolism , Spatial Learning/drug effects , Spatial Memory/drug effectsABSTRACT
Angelman Syndrome (AS) is a devastating neurological disorder caused by disruption of the maternal UBE3A gene. Ube3a protein is identified as an E3 ubiquitin ligase that shows neuron-specific imprinting. Despite extensive research evaluating the localization and basal expression profiles of Ube3a in mouse models, the molecular mechanisms whereby Ube3a deficiency results in AS are enigmatic. Using in vitro and in vivo systems we show dramatic changes in the expression of Ube3a following synaptic activation. In primary neuronal culture, neuronal depolarization was found to increase both nuclear and cytoplasmic Ube3a levels. Analogous up-regulation in maternal and paternal Ube3a expression was observed in Ube3a-YFP reporter mice following fear conditioning. Absence of Ube3a led to deficits in the activity-dependent increases in ERK1/2 phosphorylation, which may contribute to reported deficits in synaptic plasticity and cognitive function in AS mice. Taken together, our findings provide novel insight into the regulation of Ube3a by synaptic activity and its potential role in kinase regulation.
Subject(s)
Angelman Syndrome/physiopathology , Brain/physiopathology , Neurons/physiology , Ubiquitin-Protein Ligases/metabolism , Angelman Syndrome/enzymology , Animals , Cell Nucleus/metabolism , Cells, Cultured , Conditioning, Psychological , Cytoplasm/metabolism , Fear/physiology , Female , In Vitro Techniques , MAP Kinase Signaling System/physiology , Male , Membrane Potentials , Mice , Mice, Inbred C57BL , Mice, Transgenic , Parents , Synaptic Transmission , Ubiquitin-Protein Ligases/geneticsABSTRACT
Angelman syndrome (AS) is a neurogenetic disorder caused by loss of maternal UBE3A expression or mutation-induced dysfunction of its protein product, the E3 ubiquitin-protein ligase, UBE3A. In humans and rodents, UBE3A/Ube3a transcript is maternally imprinted in several brain regions, but the distribution of native UBE3A/Ube3a(1) protein expression has not been comprehensively examined. To address this, we systematically evaluated Ube3a expression in the brain and peripheral tissues of wild-type (WT) and Ube3a maternal knockout mice (AS mice). Immunoblot and immunohistochemical analyses revealed a marked loss of Ube3a protein in hippocampus, hypothalamus, olfactory bulb, cerebral cortex, striatum, thalamus, midbrain, and cerebellum in AS mice relative to WT littermates. Also, Ube3a expression in heart and liver of AS mice showed greater than the predicted 50% reduction relative to WT mice. Co-localization studies showed Ube3a expression to be primarily neuronal in all brain regions and present in GABAergic interneurons as well as principal neurons. These findings suggest that neuronal function throughout the brain is compromised in AS.
