Abstract

The incidence of neurodegenerative diseases in the developed world has risen over the last century, concomitant with an increase in average human lifespan. A major challenge is therefore to identify genes that control neuronal health and viability with a view to enhancing neuronal health during ageing and reducing the burden of neurodegeneration. Analysis of gene expression data has recently been used to infer gene functions for a range of tissues from co-expression networks. We have now applied this approach to transcriptomic datasets from the mammalian nervous system available in the public domain. We have defined the genes critical for influencing neuronal health and disease in different neurological cell types and brain regions. The functional contribution of genes in each co-expression cluster was validated using human disease and knockout mouse phenotypes, pathways and gene ontology term annotation. Additionally a number of poorly annotated genes were implicated by this approach in nervous system function. Exploiting gene expression data available in the public domain allowed us to validate key nervous system genes and, importantly, to identify additional genes with minimal functional annotation but with the same expression pattern. These genes are thus novel candidates for a role in neurological health and disease and could now be further investigated to confirm their function and regulation during ageing and neurodegeneration.

Highlights

  • The average lifespan of individuals in the developed world has increased dramatically over the last century, as deaths from trauma and infection have declined

  • We present an analysis of combined datasets of transcription in mouse tissues, revealing key genes and networks present in the mammalian nervous system, and review the literature concerning nervous system cell typespecific genetic markers

  • Gene expression patterns were clustered using the network analysis tool BioLayout Express3D to explore the relationships of the different cell and tissue types in the analysis [28]

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Summary

Introduction

The average lifespan of individuals in the developed world has increased dramatically over the last century, as deaths from trauma and infection have declined. The incidence of neurodegenerative diseases associated with ageing, including dementia, has risen concomitantly, bringing significant social and economic costs. Our understanding of genetic factors controlling nervous system form and function in health and disease is far from complete. The identification of genes that control neuronal health, and elucidation of core molecular interactions that could be exploited for the development of novel therapeutic interventions, remains a major challenge. A large proportion of genes in animals are involved in the development, differentiation, maintenance and functioning of the nervous system. In Drosophila, 11% of annotated and predicted genes showed a specific neurological phenotype upon knockdown [1] with 336 showing a strong phenotype and 2106 showing moderate to weak phenotypes

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