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Bioinformatic analysis of microRNA expression in Huntington's disease
Huntington's disease (HD) is an inherited, progressive neurodegenerative disease caused by a CAG expansion in the Huntingtin (HTT) gene and various dysfunctions of biological processes in HD have been proposed. Although monogenic, the exact pathogenesis of HD currently remains unclear. To ident...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6102687/ https://www.ncbi.nlm.nih.gov/pubmed/30015953 http://dx.doi.org/10.3892/mmr.2018.9238 |
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author | Dong, Xiaoyu Cong, Shuyan |
author_facet | Dong, Xiaoyu Cong, Shuyan |
author_sort | Dong, Xiaoyu |
collection | PubMed |
description | Huntington's disease (HD) is an inherited, progressive neurodegenerative disease caused by a CAG expansion in the Huntingtin (HTT) gene and various dysfunctions of biological processes in HD have been proposed. Although monogenic, the exact pathogenesis of HD currently remains unclear. To identify the synergistic microRNA (miRNA) pattern in HD, the miRNA expression profile dataset GSE64977 and the gene expression profile dataset GSE64810 were downloaded. Programming software R was used to identify differentially expressed genes (DEGs) and differentially expressed miRNAs (DEMs). Target genes of DEMs were predicted using the TargetScan database. Gene ontology (GO) function of DEGs was generated using the FunRich and a miRNA-mRNA interaction network was constructed using Cytoscape software. In total, 1,612 DEGs and 10 DEMs were identified. GO terms mainly included inflammatory response and immune response in DEGs. A total of 745 target genes were predicted from the DEMs and 33 overlaps were identified between these target genes and DEGs. The miRNA network demonstrated that hsa-miR-4488, hsa-miR-196a-5p, and hsa-miR-549a had a high degree and may be involved with the pathogenesis and potential therapeutic targets of HD. |
format | Online Article Text |
id | pubmed-6102687 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-61026872018-08-23 Bioinformatic analysis of microRNA expression in Huntington's disease Dong, Xiaoyu Cong, Shuyan Mol Med Rep Articles Huntington's disease (HD) is an inherited, progressive neurodegenerative disease caused by a CAG expansion in the Huntingtin (HTT) gene and various dysfunctions of biological processes in HD have been proposed. Although monogenic, the exact pathogenesis of HD currently remains unclear. To identify the synergistic microRNA (miRNA) pattern in HD, the miRNA expression profile dataset GSE64977 and the gene expression profile dataset GSE64810 were downloaded. Programming software R was used to identify differentially expressed genes (DEGs) and differentially expressed miRNAs (DEMs). Target genes of DEMs were predicted using the TargetScan database. Gene ontology (GO) function of DEGs was generated using the FunRich and a miRNA-mRNA interaction network was constructed using Cytoscape software. In total, 1,612 DEGs and 10 DEMs were identified. GO terms mainly included inflammatory response and immune response in DEGs. A total of 745 target genes were predicted from the DEMs and 33 overlaps were identified between these target genes and DEGs. The miRNA network demonstrated that hsa-miR-4488, hsa-miR-196a-5p, and hsa-miR-549a had a high degree and may be involved with the pathogenesis and potential therapeutic targets of HD. D.A. Spandidos 2018-09 2018-06-29 /pmc/articles/PMC6102687/ /pubmed/30015953 http://dx.doi.org/10.3892/mmr.2018.9238 Text en Copyright: © Dong et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made. |
spellingShingle | Articles Dong, Xiaoyu Cong, Shuyan Bioinformatic analysis of microRNA expression in Huntington's disease |
title | Bioinformatic analysis of microRNA expression in Huntington's disease |
title_full | Bioinformatic analysis of microRNA expression in Huntington's disease |
title_fullStr | Bioinformatic analysis of microRNA expression in Huntington's disease |
title_full_unstemmed | Bioinformatic analysis of microRNA expression in Huntington's disease |
title_short | Bioinformatic analysis of microRNA expression in Huntington's disease |
title_sort | bioinformatic analysis of microrna expression in huntington's disease |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6102687/ https://www.ncbi.nlm.nih.gov/pubmed/30015953 http://dx.doi.org/10.3892/mmr.2018.9238 |
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