Abstract
BackgroundIt has been reported that several brain diseases can be treated as transnosological manner implicating possible common molecular basis under those diseases. However, molecular level commonality among those brain diseases has been largely unexplored. Gene expression analyses of human brain have been used to find genes associated with brain diseases but most of those studies were restricted either to an individual disease or to a couple of diseases. In addition, identifying significant genes in such brain diseases mostly failed when it used typical methods depending on differentially expressed genes.ResultsIn this study, we used a correlation-based biclustering approach to find coexpressed gene sets in five neurodegenerative diseases and three psychiatric disorders. By using biclustering analysis, we could efficiently and fairly identified various gene sets expressed specifically in both single and multiple brain diseases. We could find 4,307 gene sets correlatively expressed in multiple brain diseases and 3,409 gene sets exclusively specified in individual brain diseases. The function enrichment analysis of those gene sets showed many new possible functional bases as well as neurological processes that are common or specific for those eight diseases.ConclusionsThis study introduces possible common molecular bases for several brain diseases, which open the opportunity to clarify the transnosological perspective assumed in brain diseases. It also showed the advantages of correlation-based biclustering analysis and accompanying function enrichment analysis for gene expression data in this type of investigation.
Highlights
It has been reported that several brain diseases can be treated as transnosological manner implicating possible common molecular basis under those diseases
This study introduces possible common molecular bases for several brain diseases, which open the opportunity to clarify the transnosological perspective assumed in brain diseases
Identification of brain disease-specific coexpressed gene sets We aimed to identify coexpressed gene sets either in brain diseases or in normal to find molecular mechanisms potentially associated with brain diseases
Summary
It has been reported that several brain diseases can be treated as transnosological manner implicating possible common molecular basis under those diseases. Most of the previous studies focused on identifying differentially expressed genes under various neurodegenerative diseases such as Alzheimer’s disease [9,10,11] Though they suggested sets of individual molecular players associated with brain disease etiology, it has been recommended to investigate system-level transcriptomic changes by identifying gene sets that show coexpression under either brain disease or normal condition in order to get more comprehensive understanding on highly complex brain diseases [8,12]. Those previous approaches were, restricted to individual brain diseases so that identification of molecular basis common to multiple brain diseases was difficult. Both integrative approach and biclustering analysis showed its utility in studies of other transcriptome data for complex diseases such as cancers [13,14] but there have not been applied to investigate brain transcriptome data
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