@article{67a4336e313e452194afd2a04da0b87b,
title = "Association between resting-state functional brain connectivity and gene expression is altered in autism spectrum disorder",
abstract = "Gene expression covaries with brain activity as measured by resting state functional magnetic resonance imaging (MRI). However, it is unclear how genomic differences driven by disease state can affect this relationship. Here, we integrate from the ABIDE I and II imaging cohorts with datasets of gene expression in brains of neurotypical individuals and individuals with autism spectrum disorder (ASD) with regionally matched brain activity measurements from fMRI datasets. We identify genes linked with brain activity whose association is disrupted in ASD. We identified a subset of genes that showed a differential developmental trajectory in individuals with ASD compared with controls. These genes are enriched in voltage-gated ion channels and inhibitory neurons, pointing to excitation-inhibition imbalance in ASD. We further assessed differences at the regional level showing that the primary visual cortex is the most affected region in ASD. Our results link disrupted brain expression patterns of individuals with ASD to brain activity and show developmental, cell type, and regional enrichment of activity linked genes.",
author = "Stefano Berto and Treacher, {Alex H.} and Emre Caglayan and Danni Luo and Haney, {Jillian R.} and Gandal, {Michael J.} and Geschwind, {Daniel H.} and Montillo, {Albert A.} and Genevieve Konopka",
note = "Funding Information: G.K. is a Jon Heighten Scholar in Autism Research and Townsend Distinguished Chair in Research on Autism Spectrum Disorders at UT Southwestern Medical Center. E.C. is a Neural Scientist Training Program Fellow in the Peter O{\textquoteright}Donnell Brain Institute at UT Southwestern. Data were generated as part of the PsychENCODE Consortium. Visit 10.7303/syn24240356 for a complete list of grants and PIs. Tissue specimens and/or data used in this research were obtained from the Autism BrainNet (formerly the Autism Tissue Program), which is sponsored by the Simons Foundation, and the University of Maryland Brain and Tissue Bank, which is a component of the NIH NeuroBiobank. We are grateful to the patients and families who participate in the tissue donation programs. Funding for this work was provided by grants to D.H.G. (NIMH R01MH110927, U01MH115746, P50-MH106438, and R01 MH-109912, R01 MH094714), grants to M.J.G. (SFARI Bridge to Independence Award, NIMH R01-MH121521, NIMH R01-MH123922, NICHD-P50-HD103557), and grants to J.R.H. (Achievement Rewards for College Scientists Foundation Los Angeles Founder Chapter, UCLA Neuroscience Interdepartmental Program). This work was also supported by the NIMH (MH102603, MH126481), NINDS (NS106447, NS115821), NHGRI (HG011641), the Simons Foundation (SFARI #573689), and the James S. McDonnell Foundation 21st Century Science Initiative in Understanding Human Cognition—Scholar Award (220020467) to G.K. Publisher Copyright: {\textcopyright} 2022, The Author(s).",
year = "2022",
month = dec,
doi = "10.1038/s41467-022-31053-5",
language = "English (US)",
volume = "13",
journal = "Nature Communications",
issn = "2041-1723",
publisher = "Nature Publishing Group",
number = "1",
}