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Integrative Analyses Identify KCNJ15 as a Candidate Gene in Patients with Epilepsy
INTRODUCTION: Although there is accumulating evidence that genetic factors play a vital role in the pathogenesis of epilepsy, few epilepsy-associated genes have been identified. Additionally, the role of KCNJ15 in epilepsy has not been evaluated so far. METHODS: Here, we performed differentially exp...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Healthcare
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9588107/ https://www.ncbi.nlm.nih.gov/pubmed/36168094 http://dx.doi.org/10.1007/s40120-022-00407-y |
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author | Wang, Shitao Li, Zongyou Ding, Xiangqian Zhao, Zongyou Zhang, Mengen Xu, Hui Lu, Jinghong Dai, Lili |
author_facet | Wang, Shitao Li, Zongyou Ding, Xiangqian Zhao, Zongyou Zhang, Mengen Xu, Hui Lu, Jinghong Dai, Lili |
author_sort | Wang, Shitao |
collection | PubMed |
description | INTRODUCTION: Although there is accumulating evidence that genetic factors play a vital role in the pathogenesis of epilepsy, few epilepsy-associated genes have been identified. Additionally, the role of KCNJ15 in epilepsy has not been evaluated so far. METHODS: Here, we performed differentially expressed gene analysis, expression quantitative trait loci analysis, gene co-expression analysis, and protein–protein interaction analysis to evaluate the role of KCNJ15 in epilepsy. RESULTS: Analysis of gene expression and expression quantitative trait loci data revealed that KCNJ15 was significantly downregulated in patients with epilepsy (adjusted P = 0.0146 and log(2) Fold change = − 1.0025), and an epilepsy-associated polymorphism (rs2833098) was linked to altered KCNJ15 expression level in human temporal lobe brain tissue (P = 0.0036). Gene co-expression analysis revealed that KCNJ15 was co-expressed with genes that have been reported to be associated with epilepsy in human brain tissue. Furthermore, protein–protein interaction analysis revealed strong supportive evidence for the role of KCNJ15 in epilepsy. CONCLUSION: Our results show that KCNJ15 may be a candidate target for epilepsy. Functional analysis of KCNJ15 may provide novel insights for epilepsy treatment. |
format | Online Article Text |
id | pubmed-9588107 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer Healthcare |
record_format | MEDLINE/PubMed |
spelling | pubmed-95881072022-11-29 Integrative Analyses Identify KCNJ15 as a Candidate Gene in Patients with Epilepsy Wang, Shitao Li, Zongyou Ding, Xiangqian Zhao, Zongyou Zhang, Mengen Xu, Hui Lu, Jinghong Dai, Lili Neurol Ther Original Research INTRODUCTION: Although there is accumulating evidence that genetic factors play a vital role in the pathogenesis of epilepsy, few epilepsy-associated genes have been identified. Additionally, the role of KCNJ15 in epilepsy has not been evaluated so far. METHODS: Here, we performed differentially expressed gene analysis, expression quantitative trait loci analysis, gene co-expression analysis, and protein–protein interaction analysis to evaluate the role of KCNJ15 in epilepsy. RESULTS: Analysis of gene expression and expression quantitative trait loci data revealed that KCNJ15 was significantly downregulated in patients with epilepsy (adjusted P = 0.0146 and log(2) Fold change = − 1.0025), and an epilepsy-associated polymorphism (rs2833098) was linked to altered KCNJ15 expression level in human temporal lobe brain tissue (P = 0.0036). Gene co-expression analysis revealed that KCNJ15 was co-expressed with genes that have been reported to be associated with epilepsy in human brain tissue. Furthermore, protein–protein interaction analysis revealed strong supportive evidence for the role of KCNJ15 in epilepsy. CONCLUSION: Our results show that KCNJ15 may be a candidate target for epilepsy. Functional analysis of KCNJ15 may provide novel insights for epilepsy treatment. Springer Healthcare 2022-09-28 /pmc/articles/PMC9588107/ /pubmed/36168094 http://dx.doi.org/10.1007/s40120-022-00407-y Text en © The Author(s) 2022 https://creativecommons.org/licenses/by-nc/4.0/Open AccessThis article is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License, which permits any non-commercial 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) . |
spellingShingle | Original Research Wang, Shitao Li, Zongyou Ding, Xiangqian Zhao, Zongyou Zhang, Mengen Xu, Hui Lu, Jinghong Dai, Lili Integrative Analyses Identify KCNJ15 as a Candidate Gene in Patients with Epilepsy |
title | Integrative Analyses Identify KCNJ15 as a Candidate Gene in Patients with Epilepsy |
title_full | Integrative Analyses Identify KCNJ15 as a Candidate Gene in Patients with Epilepsy |
title_fullStr | Integrative Analyses Identify KCNJ15 as a Candidate Gene in Patients with Epilepsy |
title_full_unstemmed | Integrative Analyses Identify KCNJ15 as a Candidate Gene in Patients with Epilepsy |
title_short | Integrative Analyses Identify KCNJ15 as a Candidate Gene in Patients with Epilepsy |
title_sort | integrative analyses identify kcnj15 as a candidate gene in patients with epilepsy |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9588107/ https://www.ncbi.nlm.nih.gov/pubmed/36168094 http://dx.doi.org/10.1007/s40120-022-00407-y |
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