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Cytoskeletal regulation by AUTS2 in neuronal migration and neuritogenesis.
- Source :
-
Cell reports [Cell Rep] 2014 Dec 24; Vol. 9 (6), pp. 2166-79. Date of Electronic Publication: 2014 Dec 18. - Publication Year :
- 2014
-
Abstract
- Mutations in the Autism susceptibility candidate 2 gene (AUTS2), whose protein is believed to act in neuronal cell nuclei, have been associated with multiple psychiatric illnesses, including autism spectrum disorders, intellectual disability, and schizophrenia. Here we show that cytoplasmic AUTS2 is involved in the regulation of the cytoskeleton and neural development. Immunohistochemistry and fractionation studies show that AUTS2 localizes not only in nuclei, but also in the cytoplasm, including in the growth cones in the developing brain. AUTS2 activates Rac1 to induce lamellipodia but downregulates Cdc42 to suppress filopodia. Our loss-of-function and rescue experiments show that a cytoplasmic AUTS2-Rac1 pathway is involved in cortical neuronal migration and neuritogenesis in the developing brain. These findings suggest that cytoplasmic AUTS2 acts as a regulator of Rho family GTPases to contribute to brain development and give insight into the pathology of human psychiatric disorders with AUTS2 mutations.<br /> (Copyright © 2014 The Authors. Published by Elsevier Inc. All rights reserved.)
- Subjects :
- Animals
Brain cytology
Brain growth & development
Brain metabolism
Cells, Cultured
Cytoskeletal Proteins
Humans
Mice
Mice, Inbred ICR
Neurons cytology
Neurons physiology
Neuropeptides metabolism
Nuclear Proteins genetics
Pseudopodia metabolism
Transcription Factors
cdc42 GTP-Binding Protein metabolism
rac1 GTP-Binding Protein metabolism
Actin Cytoskeleton metabolism
Cell Movement
Neurogenesis
Neurons metabolism
Nuclear Proteins metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 2211-1247
- Volume :
- 9
- Issue :
- 6
- Database :
- MEDLINE
- Journal :
- Cell reports
- Publication Type :
- Academic Journal
- Accession number :
- 25533347
- Full Text :
- https://doi.org/10.1016/j.celrep.2014.11.045