Abstract

Autism spectrum disorder (ASD) is a complex neuropsychiatric disorder characterized by substantial heterogeneity. To identify the convergence of disease pathology on common pathways, it is essential to understand the correlations among ASD candidate genes and study shared molecular pathways between them. Investigating functional interactions between ASD candidate genes in different cell types of normal human brains may shed new light on the genetic heterogeneity of ASD. Here we apply cell type-specific gene network-based analysis to analyze human brain nucleus gene expression data and identify cell type-specific ASD-associated gene modules. ASD-associated modules specific to different cell types are relevant to different gene functions, for instance, the astrocytes-specific module is involved in functions of axon and neuron projection guidance, GABAergic interneuron-specific modules are involved in functions of postsynaptic membrane, extracellular matrix structural constituent, and ion transmembrane transporter activity. Our findings can promote the study of cell type heterogeneity of ASD, providing new insights into the pathogenesis of ASD. Our method has been shown to be effective in discovering cell type-specific disease-associated gene expression patterns and can be applied to other complex diseases.

Highlights

  • Autism spectrum disorder (ASD) is a complex neuropsychiatric disorder with substantial phenotypic and genetic heterogeneity, characterized by impairments in social interaction and communication, and repetitive and restricted behaviors

  • To identify the convergence of ASD pathology on common pathways, it is essential to understand the correlations among ASD candidate genes and study their shared molecular pathways

  • With the hypothesis that investigating functional relationships between ASD candidate genes in normal human brains may provide convergent mechanistic insight into the genetic heterogeneity of ASD, gene co-expression network was built based on normal human brain transcriptomic data sequenced by bulk RNA sequencing (Ben-David and Shifman, 2012; Mahfouz et al, 2015)

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Summary

Introduction

Autism spectrum disorder (ASD) is a complex neuropsychiatric disorder with substantial phenotypic and genetic heterogeneity, characterized by impairments in social interaction and communication, and repetitive and restricted behaviors. Since ASD is believed to result from functional aberrations within brains, it was hypothesized that investigating functional relationships between ASD candidate genes in normal human brains may provide convergent mechanistic insight into the genetic heterogeneity of ASD (Mahfouz et al, 2015). With this hypothesis, several studies constructed a gene co-expression network based on bulk transcriptomic data of normal human brains and mapped ASD candidate genes or/and cell type markers to the gene modules, whose functions were analyzed for identifying the pathways and. It is essential to construct gene networks in a cell type-specific way for identifying the vulnerable cell types and converged pathways among ASD candidate genes in different cells

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