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

被引:153
|
作者
Tran, Helene [1 ]
Almeida, Sandra [1 ]
Moore, Jill [2 ]
Gendron, Tania F. [3 ]
Chalasani, UmaDevi [1 ]
Lu, Yubing [1 ]
Du, Xing [1 ]
Nickerson, Jeffrey A. [4 ]
Petrucelli, Leonard [3 ]
Weng, Zhiping [2 ]
Gao, Fen-Biao [1 ]
机构
[1] Univ Massachusetts, Sch Med, Dept Neurol, Worcester, MA 01605 USA
[2] Univ Massachusetts, Sch Med, Program Bioinformat & Integrat Biol, Worcester, MA 01605 USA
[3] Mayo Clin Florida, Dept Neurosci, Jacksonville, FL 32224 USA
[4] Univ Massachusetts, Sch Med, Dept Cell & Dev Biol, Worcester, MA 01605 USA
基金
美国国家卫生研究院;
关键词
HEXANUCLEOTIDE REPEAT; FRONTOTEMPORAL DEMENTIA; ANTISENSE TRANSCRIPTS; GGGGCC REPEAT; TRANSLATION; EXPANSION; ALS; C9FTD/ALS; POLY(GA); LEAD;
D O I
10.1016/j.neuron.2015.09.015
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Dipeptide repeat (DPR) proteins are toxic in various models of FTD/ALS with GGGGCC (G(4)C(2)) repeat expansion. However, it is unclear whether nuclear G(4)C(2) RNA foci also induce neurotoxicity. Here, we describe a Drosophila model expressing 160 G(4)C(2) repeats (160R) flanked by human intronic and exonic sequences. Spliced intronic 160R formed nuclear G(4)C(2) 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 G(4)C(2) RNA export and subsequent DPR production.
引用
收藏
页码:1207 / 1214
页数:8
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