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Functional dissection of human targets for KSHV-encoded miRNAs using network analysis
Kaposi’s sarcoma-associated herpesvirus (KSHV) is the etiological agent of Kaposi’s sarcoma, primary effusion lymphoma and multicentric Castleman’s disease, etc. In this study, we firstly systematically constructed the KSHV-encoded miRNA-regulated co-expressed protein-protein interaction network (Ce...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5466626/ https://www.ncbi.nlm.nih.gov/pubmed/28600495 http://dx.doi.org/10.1038/s41598-017-03462-w |
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author | Wang, Yu Lin, Yun Guo, Yanzhi Pu, Xuemei Li, Menglong |
author_facet | Wang, Yu Lin, Yun Guo, Yanzhi Pu, Xuemei Li, Menglong |
author_sort | Wang, Yu |
collection | PubMed |
description | Kaposi’s sarcoma-associated herpesvirus (KSHV) is the etiological agent of Kaposi’s sarcoma, primary effusion lymphoma and multicentric Castleman’s disease, etc. In this study, we firstly systematically constructed the KSHV-encoded miRNA-regulated co-expressed protein-protein interaction network (CePPIN), which display the biological knowledge regarding the mechanism of miRNA-regulated KSHV pathogenesis. Then, we investigated the topological parameters for the proteins in CePPIN, especially for those miRNA targets and we found that cellular target genes of KSHV-encoded miRNAs tend to be hubs and bottlenecks in the network. Then the GO and KEGG pathway analysis suggests that miRNA targets are involved in various cellular processes mostly related to immune regulate and cell cycle. Enrichment analysis was also performed to identify the six important functional modules which are proven to be highly related to KSHV pathogenesis. Finally, difference analysis of common targets and specific targets shows that two kinds of targets are different in terms of both topological properties and enriched functions, thus we can extrapolate that the functions of KSHV-encoded miRNAs can be also classified into two generic groups, one can act as functional mimics of some oncogenic human miRNAs which contribute to tumorigenesis and the other can contribute to maintaining viral survival. |
format | Online Article Text |
id | pubmed-5466626 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-54666262017-06-14 Functional dissection of human targets for KSHV-encoded miRNAs using network analysis Wang, Yu Lin, Yun Guo, Yanzhi Pu, Xuemei Li, Menglong Sci Rep Article Kaposi’s sarcoma-associated herpesvirus (KSHV) is the etiological agent of Kaposi’s sarcoma, primary effusion lymphoma and multicentric Castleman’s disease, etc. In this study, we firstly systematically constructed the KSHV-encoded miRNA-regulated co-expressed protein-protein interaction network (CePPIN), which display the biological knowledge regarding the mechanism of miRNA-regulated KSHV pathogenesis. Then, we investigated the topological parameters for the proteins in CePPIN, especially for those miRNA targets and we found that cellular target genes of KSHV-encoded miRNAs tend to be hubs and bottlenecks in the network. Then the GO and KEGG pathway analysis suggests that miRNA targets are involved in various cellular processes mostly related to immune regulate and cell cycle. Enrichment analysis was also performed to identify the six important functional modules which are proven to be highly related to KSHV pathogenesis. Finally, difference analysis of common targets and specific targets shows that two kinds of targets are different in terms of both topological properties and enriched functions, thus we can extrapolate that the functions of KSHV-encoded miRNAs can be also classified into two generic groups, one can act as functional mimics of some oncogenic human miRNAs which contribute to tumorigenesis and the other can contribute to maintaining viral survival. Nature Publishing Group UK 2017-06-09 /pmc/articles/PMC5466626/ /pubmed/28600495 http://dx.doi.org/10.1038/s41598-017-03462-w Text en © The Author(s) 2017 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/. |
spellingShingle | Article Wang, Yu Lin, Yun Guo, Yanzhi Pu, Xuemei Li, Menglong Functional dissection of human targets for KSHV-encoded miRNAs using network analysis |
title | Functional dissection of human targets for KSHV-encoded miRNAs using network analysis |
title_full | Functional dissection of human targets for KSHV-encoded miRNAs using network analysis |
title_fullStr | Functional dissection of human targets for KSHV-encoded miRNAs using network analysis |
title_full_unstemmed | Functional dissection of human targets for KSHV-encoded miRNAs using network analysis |
title_short | Functional dissection of human targets for KSHV-encoded miRNAs using network analysis |
title_sort | functional dissection of human targets for kshv-encoded mirnas using network analysis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5466626/ https://www.ncbi.nlm.nih.gov/pubmed/28600495 http://dx.doi.org/10.1038/s41598-017-03462-w |
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