Tat IRES modulator of tat mRNA (TIM-TAM): A conserved RNA structure that controls Tat expression and acts as a switch for HIV productive and latent infection

Georges Khoury, Charlene MacKenzie, Lilia Ayadi, Sharon R. Lewin, Christiane Branlant, Damian F.J. Purcell

Research output: Contribution to journalArticlepeer-review

11 Scopus citations

Abstract

Tat protein is essential to fully activate HIV transcription and processing of viral mRNA, and therefore determines virus expression in productive replication and the establishment and maintenance of latent infection. Here, we used thermodynamic and structure analyses to define a highly conserved sequence-structure in tat mRNA that functions as Tat IRES modulator of tat mRNA (TIM-TAM). By impeding cap-dependent ribosome progression during authentic spliced tat mRNA translation, TIM-TAM stable structure impacts on timing and level of Tat protein hence controlling HIV production and infectivity along with promoting latency. TIM-TAM also adopts a conformation that mediates Tat internal ribosome entry site (IRES)-dependent translation during the early phases of infection before provirus integration. Our results document the critical role of TIM-TAM in Tat expression to facilitate virus reactivation from latency, with implications for HIV treatment and drug development.

Original languageEnglish
Pages (from-to)2643-2660
Number of pages18
JournalNucleic Acids Research
Volume48
Issue number5
DOIs
StatePublished - 18 Mar 2020
Externally publishedYes

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