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JUN and PDGFRA as Crucial Candidate Genes for Childhood Autism Spectrum Disorder

Autism spectrum disorder (ASD) is a complex neurodevelopmental disorder, characterized by marked genetic heterogeneity. In this study, two independent microarray datasets of cerebellum of ASD were integrative analyzed by NetworkAnalyst to screen candidate crucial genes. NetworkAnalyst identified two...

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Autores principales: Li, Heli, Wang, Xinyuan, Hu, Cong, Li, Hao, Xu, Zhuoshuo, Lei, Ping, Luo, Xiaoping, Hao, Yan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9152672/
https://www.ncbi.nlm.nih.gov/pubmed/35655651
http://dx.doi.org/10.3389/fninf.2022.800079
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author Li, Heli
Wang, Xinyuan
Hu, Cong
Li, Hao
Xu, Zhuoshuo
Lei, Ping
Luo, Xiaoping
Hao, Yan
author_facet Li, Heli
Wang, Xinyuan
Hu, Cong
Li, Hao
Xu, Zhuoshuo
Lei, Ping
Luo, Xiaoping
Hao, Yan
author_sort Li, Heli
collection PubMed
description Autism spectrum disorder (ASD) is a complex neurodevelopmental disorder, characterized by marked genetic heterogeneity. In this study, two independent microarray datasets of cerebellum of ASD were integrative analyzed by NetworkAnalyst to screen candidate crucial genes. NetworkAnalyst identified two up-regulated genes, Jun proto-oncogene (JUN) and platelet derived growth factor receptor alpha (PDGFRA), as the most crucial genes in cerebellum of ASD patients. Based on KEGG pathway database, genes associated with JUN in the cerebellum highlight the pathways of Th17 cell differentiation and Th1 and Th2 cell differentiation. Genes associated with PDGFRA in the cerebellum were found enriched in pathways in EGFR tyrosine kinase inhibitor resistance and Rap1 signaling pathway. Analyzing all differentially expressed genes (DEGs) from the two datasets, Gene Set Enrichment Analysis (GSEA) brought out IL17 signaling pathway, which is related to the expression of JUN and PDGFRA. The ImmuCellAI found the elevated expression of JUN and PDGFRA correlating with increased Th17 and monocytes suggests JUN and PDGFRA may regulate Th17 cell activation and monocytes infiltrating. Mice model of maternal immune activation demonstrated that JUN and PDGFRA are up-regulated and related to the ASD-like behaviors that provide insights into the molecular mechanisms underlying the altered IL17 signaling pathway in ASD and may enable novel therapeutic strategies.
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spelling pubmed-91526722022-06-01 JUN and PDGFRA as Crucial Candidate Genes for Childhood Autism Spectrum Disorder Li, Heli Wang, Xinyuan Hu, Cong Li, Hao Xu, Zhuoshuo Lei, Ping Luo, Xiaoping Hao, Yan Front Neuroinform Neuroscience Autism spectrum disorder (ASD) is a complex neurodevelopmental disorder, characterized by marked genetic heterogeneity. In this study, two independent microarray datasets of cerebellum of ASD were integrative analyzed by NetworkAnalyst to screen candidate crucial genes. NetworkAnalyst identified two up-regulated genes, Jun proto-oncogene (JUN) and platelet derived growth factor receptor alpha (PDGFRA), as the most crucial genes in cerebellum of ASD patients. Based on KEGG pathway database, genes associated with JUN in the cerebellum highlight the pathways of Th17 cell differentiation and Th1 and Th2 cell differentiation. Genes associated with PDGFRA in the cerebellum were found enriched in pathways in EGFR tyrosine kinase inhibitor resistance and Rap1 signaling pathway. Analyzing all differentially expressed genes (DEGs) from the two datasets, Gene Set Enrichment Analysis (GSEA) brought out IL17 signaling pathway, which is related to the expression of JUN and PDGFRA. The ImmuCellAI found the elevated expression of JUN and PDGFRA correlating with increased Th17 and monocytes suggests JUN and PDGFRA may regulate Th17 cell activation and monocytes infiltrating. Mice model of maternal immune activation demonstrated that JUN and PDGFRA are up-regulated and related to the ASD-like behaviors that provide insights into the molecular mechanisms underlying the altered IL17 signaling pathway in ASD and may enable novel therapeutic strategies. Frontiers Media S.A. 2022-05-16 /pmc/articles/PMC9152672/ /pubmed/35655651 http://dx.doi.org/10.3389/fninf.2022.800079 Text en Copyright © 2022 Li, Wang, Hu, Li, Xu, Lei, Luo and Hao. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Li, Heli
Wang, Xinyuan
Hu, Cong
Li, Hao
Xu, Zhuoshuo
Lei, Ping
Luo, Xiaoping
Hao, Yan
JUN and PDGFRA as Crucial Candidate Genes for Childhood Autism Spectrum Disorder
title JUN and PDGFRA as Crucial Candidate Genes for Childhood Autism Spectrum Disorder
title_full JUN and PDGFRA as Crucial Candidate Genes for Childhood Autism Spectrum Disorder
title_fullStr JUN and PDGFRA as Crucial Candidate Genes for Childhood Autism Spectrum Disorder
title_full_unstemmed JUN and PDGFRA as Crucial Candidate Genes for Childhood Autism Spectrum Disorder
title_short JUN and PDGFRA as Crucial Candidate Genes for Childhood Autism Spectrum Disorder
title_sort jun and pdgfra as crucial candidate genes for childhood autism spectrum disorder
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9152672/
https://www.ncbi.nlm.nih.gov/pubmed/35655651
http://dx.doi.org/10.3389/fninf.2022.800079
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