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C9ORF72 expression and cellular localization over mouse development

Citation

Atkinson, RA and Fernandez-Martos, CM and Atkin, J and Vickers, JC and King, AE, C9ORF72 expression and cellular localization over mouse development, Acta neuropathologica communications, 3 Article 59. ISSN 2051-5960 (2015) [Refereed Article]


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Copyright Statement

Copyright 2015 Atkinson et al. Licensed under Creative Commons Attribution 4.0 International (CC BY 4.0) http://creativecommons.org/licenses/by/4.0/

DOI: doi:10.1186/s40478-015-0238-7

Abstract

INTRODUCTION: A majority of familial frontotemporal lobar dementia and amyotrophic lateral sclerosis cases are associated with a large repeat expansion in a non-coding region of the C9ORF72 gene. Currently, little is known about the normal function and the expression pattern of the C9ORF72 protein. The aims of this study were to characterize the expression pattern and cellular localization of the three reported mouse isoforms of C9orf72, over a developmental time-course in primary cultured cortical neurons and brain tissue from C57BL/6 mice.

RESULTS: We demonstrated that the different isoforms of C9ORF72 at the mRNA and protein level undergo alterations in expression during development and into adulthood. Cellular fractionation and immunofluorescence demonstrated that levels of nuclear and cytoplasmic expression of isoforms changed significantly over the time course. Additionally, immunofluorescence studies showed C9ORF72 labeling as puncta throughout neurons, extending beyond the microtubule cytoskeleton into actin-rich structures such as filopodia and growth cones. Finally, synaptosome preparations demonstrated the presence of C9ORF72 isoform 1 in synaptic-rich fractions from adult mouse brain.

CONCLUSION: In summary, the presence of C9ORF72 as puncta and within synaptic-rich fractions may indicate involvement at the synapse and differential expression of isoforms in nuclei and cytoplasm may suggest distinct roles for the isoforms. Determining the physiological role of C9ORF72 protein may help to determine the role it plays in disease.

Item Details

Item Type:Refereed Article
Keywords:Frontotemporal dementia, C9ORF72, ALS
Research Division:Medical and Health Sciences
Research Group:Neurosciences
Research Field:Cellular Nervous System
Objective Division:Health
Objective Group:Clinical Health (Organs, Diseases and Abnormal Conditions)
Objective Field:Nervous System and Disorders
Author:Atkinson, RA (Mrs Rachel Atkinson)
Author:Fernandez-Martos, CM (Dr Carmen Fernandez-Martos)
Author:Vickers, JC (Professor James Vickers)
Author:King, AE (Associate Professor Anna King)
ID Code:105372
Year Published:2015
Web of Science® Times Cited:7
Deposited By:Wicking Dementia Research and Education Centre
Deposited On:2015-12-22
Last Modified:2017-11-06
Downloads:84 View Download Statistics

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