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    Differential Toxicity of Nuclear RNA Foci versus Dipeptide Repeat Proteins in a Drosophila Model of C9ORF72 FTD/ALS

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    Authors
    Tran, Helene
    Almeida, Sandra
    Moore, Jill
    Gendron, Tania F.
    Chalasani, UmaDevi
    Lu, Yubing
    Du, Xing
    Nickerson, Jeffrey A.
    Petrucelli, Leonard
    Weng, Zhiping
    Gao, Fen-Biao
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    UMass Chan Affiliations
    Program in Bioinformatics and Integrative Biology
    Department of Cell and Developmental Biology
    Department of Neurology
    Document Type
    Journal Article
    Publication Date
    2015-09-23
    Keywords
    Amyotrophic Lateral Sclerosis
    Animals
    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
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    Link to Full Text
    http://dx.doi.org/10.1016/j.neuron.2015.09.015
    Abstract
    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 site
    DOI
    10.1016/j.neuron.2015.09.015
    Permanent Link to this Item
    http://hdl.handle.net/20.500.14038/25931
    PubMed ID
    26402604
    Related Resources
    Link to Article in PubMed
    ae974a485f413a2113503eed53cd6c53
    10.1016/j.neuron.2015.09.015
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