Journal article
DnaJ-1 and karyopherin alpha 3 suppress degeneration in a new Drosophila model of Spinocerebellar Ataxia Type 6
Human molecular genetics, Vol.24(15), pp.4385-4396
08/01/2015
DOI: 10.1093/hmg/ddv174
PMCID: PMC4492400
PMID: 25954029
Abstract
Spinocerebellar ataxia type 6 (SCA6) belongs to the family of CAG/polyglutamine (polyQ)-dependent neurodegenerative disorders. SCA6 is caused by abnormal expansion in a CAG trinucleotide repeat within exon 47 of CACNA1A, a bicistronic gene that encodes alpha 1A, a P/Q-type calcium channel subunit and a C-terminal protein, termed alpha 1ACT. Expansion of the CAG/polyQ region of CACNA1A occurs within alpha 1ACT and leads to ataxia. There are few animal models of SCA6. Here, we describe the generation and characterization of the first Drosophila melanogaster models of SCA6, which express the entire human alpha 1ACT protein with a normal or expanded polyQ. The polyQ-expanded version of alpha 1ACT recapitulates the progressively degenerative nature of SCA6 when expressed in various fly tissues and the presence of densely staining aggregates. Additional studies identify the co-chaperone DnaJ-1 as a potential therapeutic target for SCA6. Expression of DnaJ-1 potently suppresses alpha 1ACT-dependent degeneration and lethality, concomitant with decreased aggregation and reduced nuclear localization of the pathogenic protein. Mutating the nuclear importer karyopherin alpha 3 also leads to reduced toxicity from pathogenic alpha 1ACT. Little is known about the steps leading to degeneration in SCA6 and the means to protect neurons in this disease are lacking. Invertebrate animal models of SCA6 can expand our understanding of molecular sequelae related to degeneration in this disorder and lead to the rapid identification of cellular components that can be targeted to treat it.
Details
- Title: Subtitle
- DnaJ-1 and karyopherin alpha 3 suppress degeneration in a new Drosophila model of Spinocerebellar Ataxia Type 6
- Creators
- Wei-Ling Tsou - Wayne State UniversityRyan R. Hosking - Wayne State UniversityAaron A. Burr - Cancer Genetics (United States)Joanna R. Sutton - Wayne State UniversityMichelle Ouyang - Wayne State UniversityXiaofei Du - University of ChicagoChristopher M. Gomez - University of ChicagoSokol V. Todi - Wayne State University
- Resource Type
- Journal article
- Publication Details
- Human molecular genetics, Vol.24(15), pp.4385-4396
- DOI
- 10.1093/hmg/ddv174
- PMID
- 25954029
- PMCID
- PMC4492400
- NLM abbreviation
- Hum Mol Genet
- ISSN
- 0964-6906
- eISSN
- 1460-2083
- Publisher
- Oxford Univ Press
- Number of pages
- 12
- Grant note
- R01GM084947 / NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES; United States Department of Health & Human Services; National Institutes of Health (NIH) - USA; NIH National Institute of General Medical Sciences (NIGMS) T32HD007505 / EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH & HUMAN DEVELOPMENT; United States Department of Health & Human Services; National Institutes of Health (NIH) - USA; NIH Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD) R01NS33202; R01NS086778 / NINDS; United States Department of Health & Human Services; National Institutes of Health (NIH) - USA; NIH National Institute of Neurological Disorders & Stroke (NINDS) P40OD018537 / OFFICE OF THE DIRECTOR, NATIONAL INSTITUTES OF HEALTH; United States Department of Health & Human Services; National Institutes of Health (NIH) - USA R01NS086778 / NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE; United States Department of Health & Human Services; National Institutes of Health (NIH) - USA; NIH National Institute of Neurological Disorders & Stroke (NINDS)
- Language
- English
- Date published
- 08/01/2015
- Academic Unit
- Radiology
- Record Identifier
- 9984697736402771
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