Htlv-1 rex: The courier of viral messages making use of the host vehicle

Abstract

The humanT-cell leukemia virus type 1 (HTLV-1) is a retrovirus causing an aggressiveT-cell malignancy, adult T-cell leukemia (ATL). Although HTLV-1 has a compact RNA genome, it has evolved elaborate mechanisms to maximize its coding potential.The structural proteins Gag, Pro, and Pol are encoded in the unspliced form of viral mRNA, whereas the Env pro- tein is encoded in singly spliced viral mRNA. Regulatory and accessory proteins, such as Tax, Rex, p30II, p12, and p13, are translated only from fully spliced mRNA. For effective viral replication, translation from all forms of HTLV-1 transcripts has to be achieved in concert, although unspliced mRNA are extremely unstable in mammalian cells. It has been well recognized that HTLV-1 Rex enhances the stability of unspliced and singly spliced HTLV-1 mRNA by promoting nuclear export and thereby removing them from the splicing site. Rex sp′ ecifically binds to the highly structured Rex responsive element (RxRE) located at the 3 end of all HTLV-1 mRNA. Rex then binds to the cellular nuclear exporter, CRM1, via its nuclear export signal domain and the Rex-viral transcript complex is selectively exported from the nucleus to the cytoplasm for effective translation of the viral proteins. Yet, the mechanisms by which Rex inhibits the cellular splicing machinery and utilizes the cellular pathways beneficial to viral survival in the host cell have not been fully explored. Further- more, physiological impacts of Rex against homeostasis of the host cell via interactions with numerous cellular proteins have been largely left uninvestigated. In this review, we focus on the biological importance of HTLV-1 Rex in the HTLV-1 life cycle by following the historical path in the literature concerning this viral post-transcriptional regulator from its discoverytothisday. Inaddition, forfuturestudies, wediscussrecentlydiscoveredaspects of HTLV-1 Rex as a post-transcriptional regulator and its use in host cellular pathways. © 2012 Nakano and Watanabe.