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Series GSE42910 Query DataSets for GSE42910
Status Public on Apr 05, 2013
Title Distinct roles for Toll and autophagy pathways in double-stranded RNA toxicity in a Drosophila model of expanded repeat neurodegenerative diseases
Organism Drosophila melanogaster
Experiment type Expression profiling by array
Summary Dominantly inherited expanded repeat neurodegenerative diseases are typically caused by the expansion of existing variable copy number tandem repeat sequences in otherwise unrelated genes. Repeats located in translated regions encode polyglutamine that is thought to be the toxic agent, however in several instances the expanded repeat is in an untranslated region, necessitating multiple pathogenic pathways or an alternative common toxic agent. As numerous clinical features are shared by several of these diseases, and expanded repeat RNA is a common intermediary, RNA has been proposed as a common pathogenic agent. Various forms of repeat RNA are toxic in animal models, by multiple distinct pathways. In Drosophila, repeat-containing double-stranded RNA (rCAG.rCUG~100) toxicity is dependent on Dicer processing evident with the presence of single-stranded rCAG7, which have been detected in affected HD brains. Microarray analysis of Drosophila rCAG.rCUG~100 repeat RNA toxicity revealed perturbation of several pathways including innate immunity. Recent reports of elevated circulating cytokines prior to clinical onset, and age-dependent increased inflammatory signaling and microglia activation in the brain, suggest that immune activation precedes neuronal toxicity. Since the Toll pathway is activated by certain forms of RNA, we assessed the role of this pathway in RNA toxicity. We find that rCAG.rCUG~100 activates Toll signaling and that RNA toxicity is dependent on this pathway. The sensitivity of RNA toxicity to autophagy further implicates innate immune activation. Expression of rCAG.rCUG~100 was therefore directed in glial cells and found to be sufficient to cause neuronal dysfunction. Non-autonomous toxicity due to expanded repeat-containing double-stranded RNA mediated activation of innate immunity is therefore proposed as a candidate pathway for this group of human genetic diseases.
 
Overall design The heads from newly eclosed male Drosophila were used for RNA extraction and profiling on Affymetrix Drosophile Genome 2.0 microarrays. Nine samples were analysed, representing control and experimental lines. Two independent lines of rCAG.rCUG~100 double-stranded RNA were analysed in triplicate. These were compared to 4xUAS control analysed in triplicate. All transgenes were expressed using the elavII-GAL4 pan-neuronal driver. Candidates were selected from the pool of transcripts which showed a 'present' call in all samples. T-tests were performed on raw values to determine samples that showed a significant difference with a P-value < 0.05.
 
Contributor(s) Samaraweera SE, Price GR, Venter DJ, Richards RI
Citation(s) 23525903
Submission date Dec 13, 2012
Last update date May 04, 2018
Contact name Gareth Price
E-mail(s) [email protected]
Phone 61413289611
Organization name Queensland Facility for Advanced Bioinformatics
Street address Carmody Road
City Brisbane
State/province Queensland
ZIP/Postal code 4072
Country Australia
 
Platforms (1)
GPL1322 [Drosophila_2] Affymetrix Drosophila Genome 2.0 Array
Samples (9)
GSM1053259 Drosophila heads_elavII>4xUAS, triplicate repeat 1
GSM1053260 Drosophila heads_elavII>4xUAS, triplicate repeat 2
GSM1053261 Drosophila heads_elavII>4xUAS, triplicate repeat 3
Relations
BioProject PRJNA183854

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE42910_RAW.tar 19.6 Mb (http)(custom) TAR (of CEL, CHP)
GSE42910_t-test_and_log-ratio_data.txt.gz 4.7 Mb (ftp)(http) TXT
Processed data provided as supplementary file
Processed data included within Sample table
Processed data are available on Series record

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