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The biological context of HIV-1 host interactions reveals subtle insights into a system hijack
BACKGROUND: In order to replicate, HIV, like all viruses, needs to invade a host cell and hijack it for its own use, a process that involves multiple protein interactions between virus and host. The HIV-1, Human Protein Interaction Database available at NCBI's website captures this information...
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2010
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2897785/ https://www.ncbi.nlm.nih.gov/pubmed/20529270 http://dx.doi.org/10.1186/1752-0509-4-80 |
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author | Dickerson, Jonathan E Pinney, John W Robertson, David L |
author_facet | Dickerson, Jonathan E Pinney, John W Robertson, David L |
author_sort | Dickerson, Jonathan E |
collection | PubMed |
description | BACKGROUND: In order to replicate, HIV, like all viruses, needs to invade a host cell and hijack it for its own use, a process that involves multiple protein interactions between virus and host. The HIV-1, Human Protein Interaction Database available at NCBI's website captures this information from the primary literature, containing over 2,500 unique interactions. We investigate the general properties and biological context of these interactions and, thus, explore the molecular specificity of the HIV-host perturbation. In particular, we investigate (i) whether HIV preferentially interacts with highly connected and 'central' proteins, (ii) known phenotypic properties of host proteins inferred from essentiality and disease-association data, and (iii) biological context (molecular function, processes and location) of the host proteins to identify attributes most strongly associated with specific HIV interactions. RESULTS: After correcting for ascertainment bias in the literature, we demonstrate a significantly greater propensity for HIV to interact with highly connected and central host proteins. Unexpectedly, we find there are no associations between HIV interaction and inferred essentiality. Similarly, we find a tendency for HIV not to interact with proteins encoded by genes associated with disease. Crucially, we find that functional categories over-represented in HIV-host interactions are innately enriched for highly connected and central proteins in the host system. CONCLUSIONS: Our results imply that HIV's propensity to interact with highly connected and central proteins is a consequence of interactions with particular cellular functions, rather than being a direct effect of network topological properties. The lack of a propensity for interactions with phenotypically essential proteins suggests a selective pressure to minimise virulence in retroviral evolution. Thus, the specificity of HIV-host interactions is complex, and only superficially explained by network properties. |
format | Text |
id | pubmed-2897785 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-28977852010-07-07 The biological context of HIV-1 host interactions reveals subtle insights into a system hijack Dickerson, Jonathan E Pinney, John W Robertson, David L BMC Syst Biol Research article BACKGROUND: In order to replicate, HIV, like all viruses, needs to invade a host cell and hijack it for its own use, a process that involves multiple protein interactions between virus and host. The HIV-1, Human Protein Interaction Database available at NCBI's website captures this information from the primary literature, containing over 2,500 unique interactions. We investigate the general properties and biological context of these interactions and, thus, explore the molecular specificity of the HIV-host perturbation. In particular, we investigate (i) whether HIV preferentially interacts with highly connected and 'central' proteins, (ii) known phenotypic properties of host proteins inferred from essentiality and disease-association data, and (iii) biological context (molecular function, processes and location) of the host proteins to identify attributes most strongly associated with specific HIV interactions. RESULTS: After correcting for ascertainment bias in the literature, we demonstrate a significantly greater propensity for HIV to interact with highly connected and central host proteins. Unexpectedly, we find there are no associations between HIV interaction and inferred essentiality. Similarly, we find a tendency for HIV not to interact with proteins encoded by genes associated with disease. Crucially, we find that functional categories over-represented in HIV-host interactions are innately enriched for highly connected and central proteins in the host system. CONCLUSIONS: Our results imply that HIV's propensity to interact with highly connected and central proteins is a consequence of interactions with particular cellular functions, rather than being a direct effect of network topological properties. The lack of a propensity for interactions with phenotypically essential proteins suggests a selective pressure to minimise virulence in retroviral evolution. Thus, the specificity of HIV-host interactions is complex, and only superficially explained by network properties. BioMed Central 2010-06-07 /pmc/articles/PMC2897785/ /pubmed/20529270 http://dx.doi.org/10.1186/1752-0509-4-80 Text en Copyright ©2010 Dickerson 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 Dickerson, Jonathan E Pinney, John W Robertson, David L The biological context of HIV-1 host interactions reveals subtle insights into a system hijack |
title | The biological context of HIV-1 host interactions reveals subtle insights into a system hijack |
title_full | The biological context of HIV-1 host interactions reveals subtle insights into a system hijack |
title_fullStr | The biological context of HIV-1 host interactions reveals subtle insights into a system hijack |
title_full_unstemmed | The biological context of HIV-1 host interactions reveals subtle insights into a system hijack |
title_short | The biological context of HIV-1 host interactions reveals subtle insights into a system hijack |
title_sort | biological context of hiv-1 host interactions reveals subtle insights into a system hijack |
topic | Research article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2897785/ https://www.ncbi.nlm.nih.gov/pubmed/20529270 http://dx.doi.org/10.1186/1752-0509-4-80 |
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