The long-term objective of this project is to compare and contrast the defects in neuronal mRNA expression and circuit functions produced by altered Ube3a gene dosage that may underlie the behavioral phenotypes of Autism Spectrum Disorder (ASD) with maternal 15q11-13 duplication and Angelman's Syndrome (AS). Cells from 15q11-13 ASD and AS patients have excess and deficient E3 ubiquitin ligase, Ube3a, respectively. Ube3a is the sole gene expressed selectively from the maternal allele in brain. The majority of children who inherit 15q11-13 duplications from their mothers develop ASD and the more copies inherited, the more severe the impairment. Recently, we established that increasing Ube3a gene dosage alone reconstitutes the triad of autism-related behavioral deficits in mice. Angelman's Syndrome (AS), by contrast, results when children inherit maternal Ube3a gene mutations. Importantly, Ube3a also acts as a nuclear receptor co-activator regulating gene expression independent of ligase activity. Thus we hypothesized that excess Ube3a (15q dup model) acts in the nucleus to perturb the normal expression of specific neuronal genes and encoded proteins to alter circuit function and thereby generate autism-related behavioral deficits. The logical corollary is that deficiencies of nuclear Ube3a may alter gene expression to change circuit function and produce Angelman-related behavioral deficits through the same, but opposite mechanisms. Because the brain's circuitries are designed for quantitative assessment of sensory information and quantitative motor responses, it is likely that many molecules controlling circuit functions can cause graded changes in behavior when their quantities are altered. We propose Ube3a do so through a dose-dependent regulation of neuronal gene expression. Such molecular quantity variations likely underlie the intrinsic heterogeneity of behavioral disorders like ASD.
The specific aims of this R01 grant follow: (1 and 2) determine if Ube3a gene dosage causes ASD (excess Ube3a) and AS (deficient Ube3a) related behavioral deficits through its actions within the nucleus;(3) identify the cortical neuron mRNAs quantitatively regulated by excesses or deficiencies of Ube3a;and (4) identify the cortical circui dysfunctions quantitatively induced by excesses and deficiencies of Ube3a. Our methods include a novel nuclear-targeted Ube3a transgene, a neuron cell-type specific expression of Ube3a, genome wide analysis of transcripts, and identification of consensus Ube3a-gene promoter binding sites. Slice electrophysiology and neuronal morphology will examine the effects of global and cell-type specific changes and nuclear targeted changes of Ube3a gene dosage on cortical circuit function in living brain slices. This analysis will facilitate our effors to bridge from genes to circuits to behavior in the two contrasting human neurological diseases. The project promotes the agency's mission to further a deeper understanding of the neuronal cells, circuits, and genes involved in ASD and AS via genetic models. The novel molecular insights and genetic tools will facilitate development of treatments for these life-long behavioral disabilities.

Public Health Relevance

Autism spectrum disorder (ASD) is a heterogeneous group of related behavioral disorders, characterized by deficits in three core domains: communication and social interaction, and repetitive behaviors. This project seeks to learn how Ube3a, a gene within the most common genetic copy number variant found in human autism (maternal 15q11-13 duplication) affects the expression of other genes and their proteins to alter brain circuit functions underlying these behavioral disturbances. These proteins will become therapeutic targets to treat the disease.

National Institute of Health (NIH)
National Institute of Neurological Disorders and Stroke (NINDS)
Research Project (R01)
Project #
Application #
Study Section
Pathophysiological Basis of Mental Disorders and Addictions Study Section (PMDA)
Program Officer
Mamounas, Laura
Project Start
Project End
Budget Start
Budget End
Support Year
Fiscal Year
Total Cost
Indirect Cost
Beth Israel Deaconess Medical Center
United States
Zip Code
Stoppel, David C; Anderson, Matthew P (2017) Hypersociability in the Angelman syndrome mouse model. Exp Neurol 293:137-143
Krishnan, Vaishnav; Stoppel, David C; Nong, Yi et al. (2017) Autism gene Ube3a and seizures impair sociability by repressing VTA Cbln1. Nature 543:507-512
Wang, Huiyun; Zhang, Xuexin; Xue, Li et al. (2016) Low-Voltage-Activated CaV3.1 Calcium Channels Shape T Helper Cell Cytokine Profiles. Immunity 44:782-94
VanderHorst, Veronique G; Samardzic, Tamara; Saper, Clifford B et al. (2015) ?-Synuclein pathology accumulates in sacral spinal visceral sensory pathways. Ann Neurol 78:142-9
Kasten, Michael R; Anderson, Matthew P (2015) Self-regulation of adult thalamocortical neurons. J Neurophysiol 114:323-31
Khoury, Michael N; Alsop, David C; Agnihotri, Shruti P et al. (2014) Hyperintense cortical signal on magnetic resonance imaging reflects focal leukocortical encephalitis and seizure risk in progressive multifocal leukoencephalopathy. Ann Neurol 75:659-69
Boillot, Morgane; Huneau, Clément; Marsan, Elise et al. (2014) Glutamatergic neuron-targeted loss of LGI1 epilepsy gene results in seizures. Brain 137:2984-96
Smith, Stephen E P; Xu, Lin; Kasten, Michael R et al. (2012) Mutant LGI1 inhibits seizure-induced trafficking of Kv4.2 potassium channels. J Neurochem 120:611-21
Zhou, Yu-Dong; Zhang, Dawei; Ozkaynak, Ekim et al. (2012) Epilepsy gene LGI1 regulates postnatal developmental remodeling of retinogeniculate synapses. J Neurosci 32:903-10
Smith, Stephen E P; Elliott, Robin M; Anderson, Matthew P (2012) Maternal immune activation increases neonatal mouse cortex thickness and cell density. J Neuroimmune Pharmacol 7:529-32

Showing the most recent 10 out of 11 publications