Abstract

BackgroundMouse has been extensively used as a tool for investigating the onset and development of human neurological disorders. As a first step to construct a transgenic mouse model of human brain lesions, it is of fundamental importance to clarify the similarity and divergence of genetic background between non-diseased human and mouse brain tissues.MethodsWe systematically compared, based on large scale integrated microarray data, the transcriptomes of three anatomically distinct brain regions; prefrontal cortex (PFC), hippocampus (HIP) and striatum (STR), across human and mouse. The widely used DAVID web server was used to decipher the biological functions of the highly expressed genes that were identified using a previously reported approach. Venn analysis was used to depict the overlapping ratios of the notably enriched biological process (BP) terms (one-tailed Fisher’s exact test and Benjamini correction; adjusted p < 0.01) between two brain tissues. GOSemSim, an R package, was selected to perform GO semantic similarity analysis. Next, we adjusted signal intensities of orthologous genes by the total signals in all samples within species, and used one minus Pearson’s correlation coefficient to assess the expression distance. Hierarchical clustering and principal component analysis (PCA) were selected for expression pattern analysis. Lineage specific expressed orthologous genes were identified by comparison of the most extreme sub-datasets across species and further verified using reverse transcription PCR (RT-PCR) and quantitative real-time PCR (qRT-PCR).ResultsWe found that the number of the significantly enriched BP terms of the highly expressed genes in human brain regions is larger than that in mouse corresponding brain regions. The mainly involved BP terms in human brain tissues associated with protein-membrane targeting and selenium metabolism are species-specific. The overlapping ratios of all the significantly enriched BP terms between any two brain tissues across species are lower than that within species, but the pairwise semantic similarities are very high between any two brain tissues from either human or mouse. Hierarchical clustering analysis shows the biological functions of the highly expressed genes in brain tissues are more consistent within species than interspecies; whereas it shows the expression patterns of orthologous genes are evidently conserved between human and mouse equivalent brain tissues. In addition, we identified four orthologous genes (COX5B, WIF1, SLC4A10 and PLA2G7) that are species-specific, which have been widely studied and confirmed to be closely linked with neuro- physiological and pathological functions.ConclusionOur study highlights the similarities and divergences in gene function and expression between human and mouse corresponding brain regions, including PFC, HIP and STR.

Highlights

  • Neurological disorders have become serious threatens to human health and quality of life, especially in the low-to-middle-income countries [1,2]

  • We found that the number of the significantly enriched biological process (BP) terms of the highly expressed genes in human brain regions is larger than that in mouse corresponding brain regions

  • Cross-Species Analysis of Brain Transcriptomes mainly involved BP terms in human brain tissues associated with protein-membrane targeting and selenium metabolism are species-specific

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Summary

Introduction

Neurological disorders have become serious threatens to human health and quality of life, especially in the low-to-middle-income countries [1,2]. To relieve this global burden, it is of fundamental importance to design an optimal animal model to explore the underlying mechanisms of such diseases with enigmatic pathogenesis. The successful application of numerous mouse models established to study genetic risk genes involved in neurological disorders indicates deeper biological similarities between human and mouse brains. Some studies have demonstrated an divergent expression pattern of orthologous genes [7,8,9], whereas some other investigations have showed that gene expression in analogous tissues (e.g., human and mouse comparable brain tissues) is highly conserved [10,11,12]. As a first step to construct a transgenic mouse model of human brain lesions, it is of fundamental importance to clarify the similarity and divergence of genetic background between non-diseased human and mouse brain tissues

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