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Association between resting-state functional brain connectivity and gene expression is altered in autism spectrum disorder

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...

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Autores principales: Berto, Stefano, Treacher, Alex H., Caglayan, Emre, Luo, Danni, Haney, Jillian R., Gandal, Michael J., Geschwind, Daniel H., Montillo, Albert A., Konopka, Genevieve
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9184501/
https://www.ncbi.nlm.nih.gov/pubmed/35680911
http://dx.doi.org/10.1038/s41467-022-31053-5
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author Berto, Stefano
Treacher, Alex H.
Caglayan, Emre
Luo, Danni
Haney, Jillian R.
Gandal, Michael J.
Geschwind, Daniel H.
Montillo, Albert A.
Konopka, Genevieve
author_facet Berto, Stefano
Treacher, Alex H.
Caglayan, Emre
Luo, Danni
Haney, Jillian R.
Gandal, Michael J.
Geschwind, Daniel H.
Montillo, Albert A.
Konopka, Genevieve
author_sort Berto, Stefano
collection PubMed
description 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.
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spelling pubmed-91845012022-06-11 Association between resting-state functional brain connectivity and gene expression is altered in autism spectrum disorder Berto, Stefano Treacher, Alex H. Caglayan, Emre Luo, Danni Haney, Jillian R. Gandal, Michael J. Geschwind, Daniel H. Montillo, Albert A. Konopka, Genevieve Nat Commun Article 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. Nature Publishing Group UK 2022-06-09 /pmc/articles/PMC9184501/ /pubmed/35680911 http://dx.doi.org/10.1038/s41467-022-31053-5 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Berto, Stefano
Treacher, Alex H.
Caglayan, Emre
Luo, Danni
Haney, Jillian R.
Gandal, Michael J.
Geschwind, Daniel H.
Montillo, Albert A.
Konopka, Genevieve
Association between resting-state functional brain connectivity and gene expression is altered in autism spectrum disorder
title Association between resting-state functional brain connectivity and gene expression is altered in autism spectrum disorder
title_full Association between resting-state functional brain connectivity and gene expression is altered in autism spectrum disorder
title_fullStr Association between resting-state functional brain connectivity and gene expression is altered in autism spectrum disorder
title_full_unstemmed Association between resting-state functional brain connectivity and gene expression is altered in autism spectrum disorder
title_short Association between resting-state functional brain connectivity and gene expression is altered in autism spectrum disorder
title_sort association between resting-state functional brain connectivity and gene expression is altered in autism spectrum disorder
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9184501/
https://www.ncbi.nlm.nih.gov/pubmed/35680911
http://dx.doi.org/10.1038/s41467-022-31053-5
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