Differential Toxicity of Nuclear RNA Foci versus Dipeptide Repeat Proteins in a Drosophila Model of C9ORF72 FTD/ALS
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Authors
Tran, HeleneAlmeida, Sandra
Moore, Jill
Gendron, Tania F.
Chalasani, UmaDevi
Lu, Yubing
Du, Xing
Nickerson, Jeffrey A.
Petrucelli, Leonard
Weng, Zhiping
Gao, Fen-Biao
UMass Chan Affiliations
Program in Bioinformatics and Integrative BiologyDepartment of Cell and Developmental Biology
Department of Neurology
Document Type
Journal ArticlePublication Date
2015-09-23Keywords
Amyotrophic Lateral SclerosisAnimals
Animals, Genetically Modified
Dipeptides
*Disease Models, Animal
Drosophila
Drosophila Proteins
Frontotemporal Dementia
Humans
Proteins
RNA, Nuclear
ALS
C9ORF72
DPR
Drosophila
FTD
RNA foci
Ran translation
repeats
Bioinformatics
Cell Biology
Computational Biology
Computational Neuroscience
Molecular and Cellular Neuroscience
Nervous System Diseases
Neurology
Metadata
Show full item recordAbstract
Dipeptide repeat (DPR) proteins are toxic in various models of FTD/ALS with GGGGCC (G4C2) repeat expansion. However, it is unclear whether nuclear G4C2 RNA foci also induce neurotoxicity. Here, we describe a Drosophila model expressing 160 G4C2 repeats (160R) flanked by human intronic and exonic sequences. Spliced intronic 160R formed nuclear G4C2 sense RNA foci in glia and neurons about ten times more abundantly than in human neurons; however, they had little effect on global RNA processing and neuronal survival. In contrast, highly toxic 36R in the context of poly(A)(+) mRNA were exported to the cytoplasm, where DPR proteins were produced at >100-fold higher level than in 160R flies. Moreover, the modest toxicity of intronic 160R expressed at higher temperature correlated with increased DPR production, but not RNA foci. Thus, nuclear RNA foci are neutral intermediates or possibly neuroprotective through preventing G4C2 RNA export and subsequent DPR production.Source
Neuron. 2015 Sep 23;87(6):1207-14. doi: 10.1016/j.neuron.2015.09.015. Link to article on publisher's siteDOI
10.1016/j.neuron.2015.09.015Permanent Link to this Item
http://hdl.handle.net/20.500.14038/25931PubMed ID
26402604Related Resources
Link to Article in PubMedae974a485f413a2113503eed53cd6c53
10.1016/j.neuron.2015.09.015