Background Although the disease causing gene huntingtin has been known for some time, the exact cause of neuronal cell death during Huntington's disease (HD) remains unknown. One potential mechanism contributing to the massive loss of neurons in HD brains might be the unfolded protein response (UPR) which is activated by accumulation of misfolded proteins in the endoplasmic reticulum (ER). As an adaptive response, UPR upregulates transcription of chaperones, temporarily attenuating new translation and activates protein degradation via the proteasome. However, at high levels of ER stress, UPR signalling can contribute to neuronal apoptosis.
Aims Our primary aims include (a) construction of the UPR signalling network, (b) curation and bioinformatical identification of UPR target genes and finally (c) examination of HD gene expression data sets for UPR transcriptional signatures and differential regulation of UPR pathways.
Methods The UPR signalling pathway is reconstructed based on literature review and using the Unified Interactome (UniHI) database. Lists of UPR target genes detected by previous experiments or as predicted by computational analysis are compiled. This allows us to perform enrichment analysis for differential HD gene expression and to assess whether UPR expression signatures are prominent during HD pathogenesis.
Results The canonical UPR pathway is complemented with additional protein interaction data allowing us to assess its embedding into the cellular context and to identify potential modifiers as well as novel drug targets.
Conclusions The indepth systems biology analysis can give us valuable insights about the involvement of the UPR in HD.
- systems biology
- unfolded protein response (UPR)
- endoplasmic reticulum (ER) stress
- neuronal cell death
- neuronal cell loss
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