Concomitant emergence of the antisense protein gene of HIV-1 and of the pandemic

Abstract : Recent experiments provide sound arguments in favor of the in vivo expression of the AntiSense Protein (ASP) of HIV-1. This putative protein is encoded on the antisense strand of the provirus genome and entirely overlapped by the env gene with reading frame −2. The existence of ASP was suggested in 1988, but is still controversial, and its function has yet to be determined. We used a large dataset of ∼23,000 HIV-1 and SIV sequences to study the origin, evolution, and conservation of the asp gene. We found that the ASP ORF is specific to group M of HIV-1, which is responsible for the human pandemic. Moreover, the correlation between the presence of asp and the prevalence of HIV-1 groups and M subtypes appeared to be statistically significant. We then looked for evidence of selection pressure acting on asp. Using computer simulations, we showed that the conservation of the ASP ORF in the group M could not be due to chance. Standard methods were ineffective in disentangling the two selection pressures imposed by both the Env and ASP proteins—an expected outcome with overlaps in frame −2. We thus developed a method based on careful evolutionary analysis of the presence/absence of stop codons, revealing that ASP does impose significant selection pressure. All of these results support the idea that asp is the 10th gene of HIV-1 group M and indicate a correlation with the spread of the pandemic.
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Proceedings of the National Academy of Sciences of the United States of America , National Academy of Sciences, 2016, 113 (41), pp.11537-11542. 〈10.1073/pnas.1605739113〉
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Soumis le : mardi 15 novembre 2016 - 12:28:36
Dernière modification le : jeudi 11 janvier 2018 - 06:28:16

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Elodie Cassan, Anne-Muriel Arigon Chifolleau, Jean-Michel Mesnard, Antoine Gross, Olivier Gascuel. Concomitant emergence of the antisense protein gene of HIV-1 and of the pandemic. Proceedings of the National Academy of Sciences of the United States of America , National Academy of Sciences, 2016, 113 (41), pp.11537-11542. 〈10.1073/pnas.1605739113〉. 〈lirmm-01397005〉

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