Network-based prediction and analysis of HIV dependency factors.

HIV Dependency Factors (HDFs) are a class of human proteins that are essential for HIV replication, but are not lethal to the host cell when silenced. Three previous genome-wide RNAi experiments identified HDF sets with little overlap. We combine data from these three studies with a human protein in...

Full description

Bibliographic Details
Main Authors: T M Murali, Matthew D Dyer, David Badger, Brett M Tyler, Michael G Katze
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2011-09-01
Series:PLoS Computational Biology
Online Access:http://europepmc.org/articles/PMC3178628?pdf=render
id doaj-6cd5fa3b0b5145fdbede7699a15f5ccf
record_format Article
spelling doaj-6cd5fa3b0b5145fdbede7699a15f5ccf2020-11-25T02:20:15ZengPublic Library of Science (PLoS)PLoS Computational Biology1553-734X1553-73582011-09-0179e100216410.1371/journal.pcbi.1002164Network-based prediction and analysis of HIV dependency factors.T M MuraliMatthew D DyerDavid BadgerBrett M TylerMichael G KatzeHIV Dependency Factors (HDFs) are a class of human proteins that are essential for HIV replication, but are not lethal to the host cell when silenced. Three previous genome-wide RNAi experiments identified HDF sets with little overlap. We combine data from these three studies with a human protein interaction network to predict new HDFs, using an intuitive algorithm called SinkSource and four other algorithms published in the literature. Our algorithm achieves high precision and recall upon cross validation, as do the other methods. A number of HDFs that we predict are known to interact with HIV proteins. They belong to multiple protein complexes and biological processes that are known to be manipulated by HIV. We also demonstrate that many predicted HDF genes show significantly different programs of expression in early response to SIV infection in two non-human primate species that differ in AIDS progression. Our results suggest that many HDFs are yet to be discovered and that they have potential value as prognostic markers to determine pathological outcome and the likelihood of AIDS development. More generally, if multiple genome-wide gene-level studies have been performed at independent labs to study the same biological system or phenomenon, our methodology is applicable to interpret these studies simultaneously in the context of molecular interaction networks and to ask if they reinforce or contradict each other.http://europepmc.org/articles/PMC3178628?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author T M Murali
Matthew D Dyer
David Badger
Brett M Tyler
Michael G Katze
spellingShingle T M Murali
Matthew D Dyer
David Badger
Brett M Tyler
Michael G Katze
Network-based prediction and analysis of HIV dependency factors.
PLoS Computational Biology
author_facet T M Murali
Matthew D Dyer
David Badger
Brett M Tyler
Michael G Katze
author_sort T M Murali
title Network-based prediction and analysis of HIV dependency factors.
title_short Network-based prediction and analysis of HIV dependency factors.
title_full Network-based prediction and analysis of HIV dependency factors.
title_fullStr Network-based prediction and analysis of HIV dependency factors.
title_full_unstemmed Network-based prediction and analysis of HIV dependency factors.
title_sort network-based prediction and analysis of hiv dependency factors.
publisher Public Library of Science (PLoS)
series PLoS Computational Biology
issn 1553-734X
1553-7358
publishDate 2011-09-01
description HIV Dependency Factors (HDFs) are a class of human proteins that are essential for HIV replication, but are not lethal to the host cell when silenced. Three previous genome-wide RNAi experiments identified HDF sets with little overlap. We combine data from these three studies with a human protein interaction network to predict new HDFs, using an intuitive algorithm called SinkSource and four other algorithms published in the literature. Our algorithm achieves high precision and recall upon cross validation, as do the other methods. A number of HDFs that we predict are known to interact with HIV proteins. They belong to multiple protein complexes and biological processes that are known to be manipulated by HIV. We also demonstrate that many predicted HDF genes show significantly different programs of expression in early response to SIV infection in two non-human primate species that differ in AIDS progression. Our results suggest that many HDFs are yet to be discovered and that they have potential value as prognostic markers to determine pathological outcome and the likelihood of AIDS development. More generally, if multiple genome-wide gene-level studies have been performed at independent labs to study the same biological system or phenomenon, our methodology is applicable to interpret these studies simultaneously in the context of molecular interaction networks and to ask if they reinforce or contradict each other.
url http://europepmc.org/articles/PMC3178628?pdf=render
work_keys_str_mv AT tmmurali networkbasedpredictionandanalysisofhivdependencyfactors
AT matthewddyer networkbasedpredictionandanalysisofhivdependencyfactors
AT davidbadger networkbasedpredictionandanalysisofhivdependencyfactors
AT brettmtyler networkbasedpredictionandanalysisofhivdependencyfactors
AT michaelgkatze networkbasedpredictionandanalysisofhivdependencyfactors
_version_ 1724872627806273536