Integrative Functional Genomic Analyses Implicate Specific Molecular Pathways and Circuits in Autism
Author(s) -
Neelroop Parikshak,
Rui Luo,
Alice Zhang,
Hyejung Won,
Jennifer K. Lowe,
Vijayendran Chandran,
Steve Horvath,
Daniel H. Geschwind
Publication year - 2013
Publication title -
cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 26.304
H-Index - 776
eISSN - 1097-4172
pISSN - 0092-8674
DOI - 10.1016/j.cell.2013.10.031
Subject(s) - biology , autism spectrum disorder , autism , gene , phenotype , genetics , glutamatergic , neuroscience , gene regulatory network , transcription factor , computational biology , gene expression , psychology , developmental psychology , glutamate receptor , receptor
Genetic studies have identified dozens of autism spectrum disorder (ASD) susceptibility genes, raising two critical questions: (1) do these genetic loci converge on specific biological processes, and (2) where does the phenotypic specificity of ASD arise, given its genetic overlap with intellectual disability (ID)? To address this, we mapped ASD and ID risk genes onto coexpression networks representing developmental trajectories and transcriptional profiles representing fetal and adult cortical laminae. ASD genes tightly coalesce in modules that implicate distinct biological functions during human cortical development, including early transcriptional regulation and synaptic development. Bioinformatic analyses suggest that translational regulation by FMRP and transcriptional coregulation by common transcription factors connect these processes. At a circuit level, ASD genes are enriched in superficial cortical layers and glutamatergic projection neurons. Furthermore, we show that the patterns of ASD and ID risk genes are distinct, providing a biological framework for further investigating the pathophysiology of ASD.
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