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Peripheral gene interactions define interpretable clusters of core ASD genes in a network-based investigation of the omnigenic theory

According to the recently proposed omnigenic theory, all expressed genes in a relevant tissue are contributing directly or indirectly to the manifestation of complex disorders such as autism. Thus, holistic approaches can be complementary in studying genetics of these complex disorders to focusing o...

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Autores principales: Fóthi, Ábel, Pintér, Csaba, Pollner, Péter, Lőrincz, András
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9365765/
https://www.ncbi.nlm.nih.gov/pubmed/35948596
http://dx.doi.org/10.1038/s41540-022-00240-x
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author Fóthi, Ábel
Pintér, Csaba
Pollner, Péter
Lőrincz, András
author_facet Fóthi, Ábel
Pintér, Csaba
Pollner, Péter
Lőrincz, András
author_sort Fóthi, Ábel
collection PubMed
description According to the recently proposed omnigenic theory, all expressed genes in a relevant tissue are contributing directly or indirectly to the manifestation of complex disorders such as autism. Thus, holistic approaches can be complementary in studying genetics of these complex disorders to focusing on a limited number of candidate genes. Gene interaction networks can be used for holistic studies of the omnigenic nature of autism. We used Louvain clustering on tissue-specific gene interaction networks and their subgraphs exclusively containing autism-related genes to study the effects of peripheral gene interactions. We observed that the autism gene clusters are significantly weaker connected to each other and the peripheral genes in non-neuronal tissues than in brain-related tissues. The biological functions of the brain clusters correlated well with previous findings on autism, such as synaptic signaling, regulation of DNA methylation, or regulation of lymphocyte activation, however, on the other tissues they did not enrich as significantly. Furthermore, ASD subjects with disruptive mutations in specific gene clusters show phenotypical differences compared to other disruptive variants carrying ASD individuals. Our results strengthen the omnigenic theory and can advance our understanding of the genetic background of autism.
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spelling pubmed-93657652022-08-12 Peripheral gene interactions define interpretable clusters of core ASD genes in a network-based investigation of the omnigenic theory Fóthi, Ábel Pintér, Csaba Pollner, Péter Lőrincz, András NPJ Syst Biol Appl Article According to the recently proposed omnigenic theory, all expressed genes in a relevant tissue are contributing directly or indirectly to the manifestation of complex disorders such as autism. Thus, holistic approaches can be complementary in studying genetics of these complex disorders to focusing on a limited number of candidate genes. Gene interaction networks can be used for holistic studies of the omnigenic nature of autism. We used Louvain clustering on tissue-specific gene interaction networks and their subgraphs exclusively containing autism-related genes to study the effects of peripheral gene interactions. We observed that the autism gene clusters are significantly weaker connected to each other and the peripheral genes in non-neuronal tissues than in brain-related tissues. The biological functions of the brain clusters correlated well with previous findings on autism, such as synaptic signaling, regulation of DNA methylation, or regulation of lymphocyte activation, however, on the other tissues they did not enrich as significantly. Furthermore, ASD subjects with disruptive mutations in specific gene clusters show phenotypical differences compared to other disruptive variants carrying ASD individuals. Our results strengthen the omnigenic theory and can advance our understanding of the genetic background of autism. Nature Publishing Group UK 2022-08-10 /pmc/articles/PMC9365765/ /pubmed/35948596 http://dx.doi.org/10.1038/s41540-022-00240-x 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
Fóthi, Ábel
Pintér, Csaba
Pollner, Péter
Lőrincz, András
Peripheral gene interactions define interpretable clusters of core ASD genes in a network-based investigation of the omnigenic theory
title Peripheral gene interactions define interpretable clusters of core ASD genes in a network-based investigation of the omnigenic theory
title_full Peripheral gene interactions define interpretable clusters of core ASD genes in a network-based investigation of the omnigenic theory
title_fullStr Peripheral gene interactions define interpretable clusters of core ASD genes in a network-based investigation of the omnigenic theory
title_full_unstemmed Peripheral gene interactions define interpretable clusters of core ASD genes in a network-based investigation of the omnigenic theory
title_short Peripheral gene interactions define interpretable clusters of core ASD genes in a network-based investigation of the omnigenic theory
title_sort peripheral gene interactions define interpretable clusters of core asd genes in a network-based investigation of the omnigenic theory
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9365765/
https://www.ncbi.nlm.nih.gov/pubmed/35948596
http://dx.doi.org/10.1038/s41540-022-00240-x
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