Integrative Functional Genomic Analyses Implicate Specific Molecular Pathways and Circuits in Autism

被引:757
作者
Parikshak, Neelroop N. [1 ,2 ]
Luo, Rui [3 ,4 ]
Zhang, Alice [2 ]
Won, Hyejung [1 ]
Lowe, Jennifer K. [1 ,4 ]
Chandran, Vijayendran [5 ]
Horvath, Steve [3 ,6 ]
Geschwind, Daniel H. [1 ,2 ,3 ,4 ,5 ]
机构
[1] Univ Calif Los Angeles, David Geffen Sch Med, Semel Inst, Program Neurobehav Genet, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, Interdept Program Neurosci, Los Angeles, CA 90095 USA
[3] Univ Calif Los Angeles, David Geffen Sch Med, Dept Human Genet, Los Angeles, CA 90095 USA
[4] Univ Calif Los Angeles, David Geffen Sch Med, Semel Inst, Ctr Autism Treatment & Res, Los Angeles, CA 90095 USA
[5] Univ Calif Los Angeles, David Geffen Sch Med, Dept Neurol, Program Neurogenet, Los Angeles, CA 90095 USA
[6] Univ Calif Los Angeles, Dept Biostat, Los Angeles, CA 90095 USA
关键词
COMMON GENETIC-VARIANTS; DE-NOVO MUTATIONS; TRANSCRIPTIONAL REGULATION; INTELLECTUAL DISABILITY; BRAIN-DEVELOPMENT; MESSENGER-RNAS; SPECTRUM; NETWORK; COEXPRESSION; PATTERNS;
D O I
10.1016/j.cell.2013.10.031
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:1008 / 1021
页数:14
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