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Potential role of genomic imprinted genes and brain developmental related genes in autism

BACKGROUND: Autism is a complex disease involving both environmental and genetic factors. Recent efforts have implicated the correlation of genomic imprinting and brain development in autism, however the pathogenesis of autism is not completely clear. Here, we used bioinformatic tools to provide a c...

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Autores principales: Li, Jian, Lin, Xue, Wang, Mingya, Hu, Yunyun, Xue, Kaiyu, Gu, Shuanglin, Lv, Li, Huang, Saijun, Xie, Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7099798/
https://www.ncbi.nlm.nih.gov/pubmed/32216802
http://dx.doi.org/10.1186/s12920-020-0693-2
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author Li, Jian
Lin, Xue
Wang, Mingya
Hu, Yunyun
Xue, Kaiyu
Gu, Shuanglin
Lv, Li
Huang, Saijun
Xie, Wei
author_facet Li, Jian
Lin, Xue
Wang, Mingya
Hu, Yunyun
Xue, Kaiyu
Gu, Shuanglin
Lv, Li
Huang, Saijun
Xie, Wei
author_sort Li, Jian
collection PubMed
description BACKGROUND: Autism is a complex disease involving both environmental and genetic factors. Recent efforts have implicated the correlation of genomic imprinting and brain development in autism, however the pathogenesis of autism is not completely clear. Here, we used bioinformatic tools to provide a comprehensive analysis of the autism-related genes, genomic imprinted genes and the spatially and temporally differentially expressed genes of human brain, aiming to explore the relationship between autism, brain development and genomic imprinting. METHODS: This study analyzed the distribution correlation between autism-related genes and imprinted genes on chromosomes using sliding windows and statistical methods. The normal brains’ gene expression microarray data were reanalyzed to construct a spatio-temporal coordinate system of gene expression during brain development. Finally, we intersected the autism-related genes, imprinted genes and brain spatio-temporally differentially expressed genes for further analysis to find the major biological processes that these genes involved. RESULTS: We found a positive correlation between the autism-related genes’ and imprinted genes’ distribution on chromosomes. Through the analysis of the normal brain microarray data, we constructed a spatio-temporal coordinate system of gene expression during human brain development, and obtained 13 genes that are differentially expressed in the process of brain development, which are both autism-related genes and imprinted genes. Furthermore, enrichment analysis illustrated that these genes are mainly involved in the biological processes, such as gamma-aminobutyric acid signaling pathway, neuron recognition, learning or memory, and regulation of synaptic transmission. Bioinformatic analysis implied that imprinted genes regulate the development and behavior of the brain. And its own mutation or changes in the epigenetic modification state of the imprinted control region could lead to some diseases, indicating that imprinted genes and brain development play an important role in diagnosis and prognosis of autism. CONCLUSION: This study systematically correlates brain development and genomic imprinting with autism, which provides a new perspective for the study of genetic mechanisms of autism, and selected the potential candidate biomarkers for early diagnosis of autism in clinic.
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spelling pubmed-70997982020-03-30 Potential role of genomic imprinted genes and brain developmental related genes in autism Li, Jian Lin, Xue Wang, Mingya Hu, Yunyun Xue, Kaiyu Gu, Shuanglin Lv, Li Huang, Saijun Xie, Wei BMC Med Genomics Research Article BACKGROUND: Autism is a complex disease involving both environmental and genetic factors. Recent efforts have implicated the correlation of genomic imprinting and brain development in autism, however the pathogenesis of autism is not completely clear. Here, we used bioinformatic tools to provide a comprehensive analysis of the autism-related genes, genomic imprinted genes and the spatially and temporally differentially expressed genes of human brain, aiming to explore the relationship between autism, brain development and genomic imprinting. METHODS: This study analyzed the distribution correlation between autism-related genes and imprinted genes on chromosomes using sliding windows and statistical methods. The normal brains’ gene expression microarray data were reanalyzed to construct a spatio-temporal coordinate system of gene expression during brain development. Finally, we intersected the autism-related genes, imprinted genes and brain spatio-temporally differentially expressed genes for further analysis to find the major biological processes that these genes involved. RESULTS: We found a positive correlation between the autism-related genes’ and imprinted genes’ distribution on chromosomes. Through the analysis of the normal brain microarray data, we constructed a spatio-temporal coordinate system of gene expression during human brain development, and obtained 13 genes that are differentially expressed in the process of brain development, which are both autism-related genes and imprinted genes. Furthermore, enrichment analysis illustrated that these genes are mainly involved in the biological processes, such as gamma-aminobutyric acid signaling pathway, neuron recognition, learning or memory, and regulation of synaptic transmission. Bioinformatic analysis implied that imprinted genes regulate the development and behavior of the brain. And its own mutation or changes in the epigenetic modification state of the imprinted control region could lead to some diseases, indicating that imprinted genes and brain development play an important role in diagnosis and prognosis of autism. CONCLUSION: This study systematically correlates brain development and genomic imprinting with autism, which provides a new perspective for the study of genetic mechanisms of autism, and selected the potential candidate biomarkers for early diagnosis of autism in clinic. BioMed Central 2020-03-26 /pmc/articles/PMC7099798/ /pubmed/32216802 http://dx.doi.org/10.1186/s12920-020-0693-2 Text en © The Author(s). 2020 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Li, Jian
Lin, Xue
Wang, Mingya
Hu, Yunyun
Xue, Kaiyu
Gu, Shuanglin
Lv, Li
Huang, Saijun
Xie, Wei
Potential role of genomic imprinted genes and brain developmental related genes in autism
title Potential role of genomic imprinted genes and brain developmental related genes in autism
title_full Potential role of genomic imprinted genes and brain developmental related genes in autism
title_fullStr Potential role of genomic imprinted genes and brain developmental related genes in autism
title_full_unstemmed Potential role of genomic imprinted genes and brain developmental related genes in autism
title_short Potential role of genomic imprinted genes and brain developmental related genes in autism
title_sort potential role of genomic imprinted genes and brain developmental related genes in autism
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7099798/
https://www.ncbi.nlm.nih.gov/pubmed/32216802
http://dx.doi.org/10.1186/s12920-020-0693-2
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