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Characterization the regulation of herpesvirus miRNAs from the view of human protein interaction network
BACKGROUND: miRNAs are a class of non-coding RNA molecules that play crucial roles in the regulation of virus-host interactions. The ever-increasing data of known viral miRNAs and human protein interaction network (PIN) has made it possible to study the targeting characteristics of viral miRNAs in t...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3125315/ https://www.ncbi.nlm.nih.gov/pubmed/21668952 http://dx.doi.org/10.1186/1752-0509-5-93 |
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author | Li, Zhenpeng Li, Fei Ni, Ming Li, Peng Bo, Xiaochen Wang, Shengqi |
author_facet | Li, Zhenpeng Li, Fei Ni, Ming Li, Peng Bo, Xiaochen Wang, Shengqi |
author_sort | Li, Zhenpeng |
collection | PubMed |
description | BACKGROUND: miRNAs are a class of non-coding RNA molecules that play crucial roles in the regulation of virus-host interactions. The ever-increasing data of known viral miRNAs and human protein interaction network (PIN) has made it possible to study the targeting characteristics of viral miRNAs in the context of these networks. RESULTS: We performed topological analysis to explore the targeting propensities of herpesvirus miRNAs from the view of human PIN and found that (1) herpesvirus miRNAs significantly target more hubs, moreover, compared with non-hubs (non-bottlenecks), hubs (bottlenecks) are targeted by much more virus miRNAs and virus types. (2) There are significant differences in the degree and betweenness centrality between common and specific targets, specifically we observed a significant positive correlation between virus types targeting these nodes and the proportion of hubs, and (3) K-core and ER analysis determined that common targets are closer to the global PIN center. Compared with random conditions, the giant connected component (GCC) and the density of the sub-network formed by common targets have significantly higher values, indicating the module characteristic of these targets. CONCLUSIONS: Herpesvirus miRNAs preferentially target hubs and bottlenecks. There are significant differences between common and specific targets. Moreover, common targets are more intensely connected and occupy the central part of the network. These results will help unravel the complex mechanism of herpesvirus-host interactions and may provide insight into the development of novel anti-herpesvirus drugs. |
format | Online Article Text |
id | pubmed-3125315 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-31253152011-06-29 Characterization the regulation of herpesvirus miRNAs from the view of human protein interaction network Li, Zhenpeng Li, Fei Ni, Ming Li, Peng Bo, Xiaochen Wang, Shengqi BMC Syst Biol Research Article BACKGROUND: miRNAs are a class of non-coding RNA molecules that play crucial roles in the regulation of virus-host interactions. The ever-increasing data of known viral miRNAs and human protein interaction network (PIN) has made it possible to study the targeting characteristics of viral miRNAs in the context of these networks. RESULTS: We performed topological analysis to explore the targeting propensities of herpesvirus miRNAs from the view of human PIN and found that (1) herpesvirus miRNAs significantly target more hubs, moreover, compared with non-hubs (non-bottlenecks), hubs (bottlenecks) are targeted by much more virus miRNAs and virus types. (2) There are significant differences in the degree and betweenness centrality between common and specific targets, specifically we observed a significant positive correlation between virus types targeting these nodes and the proportion of hubs, and (3) K-core and ER analysis determined that common targets are closer to the global PIN center. Compared with random conditions, the giant connected component (GCC) and the density of the sub-network formed by common targets have significantly higher values, indicating the module characteristic of these targets. CONCLUSIONS: Herpesvirus miRNAs preferentially target hubs and bottlenecks. There are significant differences between common and specific targets. Moreover, common targets are more intensely connected and occupy the central part of the network. These results will help unravel the complex mechanism of herpesvirus-host interactions and may provide insight into the development of novel anti-herpesvirus drugs. BioMed Central 2011-06-13 /pmc/articles/PMC3125315/ /pubmed/21668952 http://dx.doi.org/10.1186/1752-0509-5-93 Text en Copyright ©2011 Li et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Li, Zhenpeng Li, Fei Ni, Ming Li, Peng Bo, Xiaochen Wang, Shengqi Characterization the regulation of herpesvirus miRNAs from the view of human protein interaction network |
title | Characterization the regulation of herpesvirus miRNAs from the view of human protein interaction network |
title_full | Characterization the regulation of herpesvirus miRNAs from the view of human protein interaction network |
title_fullStr | Characterization the regulation of herpesvirus miRNAs from the view of human protein interaction network |
title_full_unstemmed | Characterization the regulation of herpesvirus miRNAs from the view of human protein interaction network |
title_short | Characterization the regulation of herpesvirus miRNAs from the view of human protein interaction network |
title_sort | characterization the regulation of herpesvirus mirnas from the view of human protein interaction network |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3125315/ https://www.ncbi.nlm.nih.gov/pubmed/21668952 http://dx.doi.org/10.1186/1752-0509-5-93 |
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