Incorrect dosage of IQSEC2, a known intellectual disability and epilepsy gene, disrupts dendritic spine morphogenesis
| Autor: | Susan J Hinze, Shervi Lie, Matilda R. Jackson, Simon C. Barry, Lachlan A. Jolly, Robert J. Harvey, Cheryl Shoubridge, Michael Field |
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| Rok vydání: | 2017 |
| Předmět: |
Male
0301 basic medicine Dendritic spine Dendritic Spines Neurogenesis Dendritic spine morphogenesis Nerve Tissue Proteins Biology Hippocampus Small hairpin RNA Mice 03 medical and health sciences Cellular and Molecular Neuroscience 0302 clinical medicine Intellectual Disability medicine Animals Guanine Nucleotide Exchange Factors RNA Small Interfering Axon Biological Psychiatry Mice Knockout Neurons Gene knockdown Epilepsy Dendrites Phenotype Cell biology Psychiatry and Mental health 030104 developmental biology medicine.anatomical_structure Mutation Knockout mouse Female Original Article Neuroscience 030217 neurology & neurosurgery |
| Zdroj: | Translational Psychiatry |
| ISSN: | 2158-3188 |
| DOI: | 10.1038/tp.2017.81 |
| Popis: | There is considerable genetic and phenotypic heterogeneity associated with intellectual disability (ID), specific learning disabilities, attention-deficit hyperactivity disorder, autism and epilepsy. The intelligence quotient (IQ) motif and SEC7 domain containing protein 2 gene (IQSEC2) is located on the X-chromosome and harbors mutations that contribute to non-syndromic ID with and without early-onset seizure phenotypes in both sexes. Although IQ and Sec7 domain mutations lead to partial loss of IQSEC2 enzymatic activity, the in vivo pathogenesis resulting from these mutations is not known. Here we reveal that IQSEC2 has a key role in dendritic spine morphology. Partial loss-of-function mutations were modeled using a lentiviral short hairpin RNA (shRNA) approach, which achieved a 57% knockdown of Iqsec2 expression in primary hippocampal cell cultures from mice. Investigating gross morphological parameters after 8 days of in vitro culture (8DIV) identified a 32% reduction in primary axon length, in contrast to a 27% and 31% increase in the number and complexity of dendrites protruding from the cell body, respectively. This increase in dendritic complexity and spread was carried through dendritic spine development, with a 34% increase in the number of protrusions per dendritic segment compared with controls at 15DIV. Although the number of dendritic spines had normalized by 21DIV, a reduction was noted in the number of immature spines. In contrast, when modeling increased dosage, overexpression of wild-type IQSEC2 led to neurons with shorter axons that were more compact and displayed simpler dendritic branching. Disturbances to dendritic morphology due to knockdown of Iqsec2 were recapitulated in neurons from Iqsec2 knockout mice generated in our laboratory using CRISPR/Cas9 technology. These observations provide evidence of dosage sensitivity for IQSEC2, which normally escapes X-inactivation in females, and links these disturbances in expression to alterations in the morphology of developing neurons. |
| Databáze: | OpenAIRE |
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