Mapping of positive selection sites in the HIV-1 genome in the context of RNA and protein structural constraints
<p>Abstract</p> <p>Background</p> <p>The HIV-1 genome is subject to pressures that target the virus resulting in escape and adaptation. On the other hand, there is a requirement for sequence conservation because of functional and structural constraints. Mapping the site...
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doaj-dd6802326fba496a80e4401c398998842020-11-25T00:52:16ZengBMCRetrovirology1742-46902011-11-01818710.1186/1742-4690-8-87Mapping of positive selection sites in the HIV-1 genome in the context of RNA and protein structural constraintsSnoeck JokeFellay JacquesBartha IstvánDouek Daniel CTelenti Amalio<p>Abstract</p> <p>Background</p> <p>The HIV-1 genome is subject to pressures that target the virus resulting in escape and adaptation. On the other hand, there is a requirement for sequence conservation because of functional and structural constraints. Mapping the sites of selective pressure and conservation on the viral genome generates a reference for understanding the limits to viral escape, and can serve as a template for the discovery of sites of genetic conflict with known or unknown host proteins.</p> <p>Results</p> <p>To build a thorough evolutionary, functional and structural map of the HIV-1 genome, complete subtype B sequences were obtained from the Los Alamos database. We mapped sites under positive selective pressure, amino acid conservation, protein and RNA structure, overlapping coding frames, CD8 T cell, CD4 T cell and antibody epitopes, and sites enriched in AG and AA dinucleotide motives. Globally, 33% of amino acid positions were found to be variable and 12% of the genome was under positive selection. Because interrelated constraining and diversifying forces shape the viral genome, we included the variables from both classes of pressure in a multivariate model to predict conservation or positive selection: structured RNA and α-helix domains independently predicted conservation while CD4 T cell and antibody epitopes were associated with positive selection.</p> <p>Conclusions</p> <p>The global map of the viral genome contains positive selected sites that are not in canonical CD8 T cell, CD4 T cell or antibody epitopes; thus, it identifies a class of residues that may be targeted by other host selective pressures. Overall, RNA structure represents the strongest determinant of HIV-1 conservation. These data can inform the combined analysis of host and viral genetic information.</p> http://www.retrovirology.com/content/8/1/87HIVevolutionpositive selectionRNA structure |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Snoeck Joke Fellay Jacques Bartha István Douek Daniel C Telenti Amalio |
spellingShingle |
Snoeck Joke Fellay Jacques Bartha István Douek Daniel C Telenti Amalio Mapping of positive selection sites in the HIV-1 genome in the context of RNA and protein structural constraints Retrovirology HIV evolution positive selection RNA structure |
author_facet |
Snoeck Joke Fellay Jacques Bartha István Douek Daniel C Telenti Amalio |
author_sort |
Snoeck Joke |
title |
Mapping of positive selection sites in the HIV-1 genome in the context of RNA and protein structural constraints |
title_short |
Mapping of positive selection sites in the HIV-1 genome in the context of RNA and protein structural constraints |
title_full |
Mapping of positive selection sites in the HIV-1 genome in the context of RNA and protein structural constraints |
title_fullStr |
Mapping of positive selection sites in the HIV-1 genome in the context of RNA and protein structural constraints |
title_full_unstemmed |
Mapping of positive selection sites in the HIV-1 genome in the context of RNA and protein structural constraints |
title_sort |
mapping of positive selection sites in the hiv-1 genome in the context of rna and protein structural constraints |
publisher |
BMC |
series |
Retrovirology |
issn |
1742-4690 |
publishDate |
2011-11-01 |
description |
<p>Abstract</p> <p>Background</p> <p>The HIV-1 genome is subject to pressures that target the virus resulting in escape and adaptation. On the other hand, there is a requirement for sequence conservation because of functional and structural constraints. Mapping the sites of selective pressure and conservation on the viral genome generates a reference for understanding the limits to viral escape, and can serve as a template for the discovery of sites of genetic conflict with known or unknown host proteins.</p> <p>Results</p> <p>To build a thorough evolutionary, functional and structural map of the HIV-1 genome, complete subtype B sequences were obtained from the Los Alamos database. We mapped sites under positive selective pressure, amino acid conservation, protein and RNA structure, overlapping coding frames, CD8 T cell, CD4 T cell and antibody epitopes, and sites enriched in AG and AA dinucleotide motives. Globally, 33% of amino acid positions were found to be variable and 12% of the genome was under positive selection. Because interrelated constraining and diversifying forces shape the viral genome, we included the variables from both classes of pressure in a multivariate model to predict conservation or positive selection: structured RNA and α-helix domains independently predicted conservation while CD4 T cell and antibody epitopes were associated with positive selection.</p> <p>Conclusions</p> <p>The global map of the viral genome contains positive selected sites that are not in canonical CD8 T cell, CD4 T cell or antibody epitopes; thus, it identifies a class of residues that may be targeted by other host selective pressures. Overall, RNA structure represents the strongest determinant of HIV-1 conservation. These data can inform the combined analysis of host and viral genetic information.</p> |
topic |
HIV evolution positive selection RNA structure |
url |
http://www.retrovirology.com/content/8/1/87 |
work_keys_str_mv |
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