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Temporal regulation of HTLV-2 expression in infected cell lines and patients: evidence for distinct expression kinetics with nuclear accumulation of APH-2 mRNA

Authors :
Bender Cecilia
Rende Francesca
Cotena Alessia
Righi Paola
Ronzi Paola
Cavallari Ilaria
Casoli Claudio
Ciminale Vincenzo
Bertazzoni Umberto
Source :
Retrovirology, Vol 9, Iss 1, p 74 (2012)
Publication Year :
2012
Publisher :
BMC, 2012.

Abstract

Abstract Background Human T-cell leukemia virus types 1 and 2 (HTLV-1 and HTLV-2) are delta retroviruses with similar genetic organization. Although both viruses immortalize T-cells in vitro, they exhibit distinct pathogenic potential in vivo. To search for possible differences in its expression strategy with respect to HTLV-1, we investigated the pattern of HTLV-2 expression in infected cell lines and peripheral blood mononuclear cells (PBMCs) from infected patients using splice site-specific quantitative RT-PCR. Findings A novel alternative splice acceptor site for exon 2 was identified; its usage in env transcripts was found to be subtype-specific. Time-course analysis revealed a two-phase expression kinetics in an infected cell line and in PBMCs of two of the three patients examined; this pattern was reminiscent of HTLV-1. In addition, the minus-strand APH2 transcript was mainly detected in the nucleus, a feature that was similar to its HTLV-1 orthologue HBZ. In contrast to HTLV-1, expression of the mRNA encoding the main regulatory proteins Tax and Rex and that of the mRNAs encoding the p28 and truncated Rex inhibitors is skewed towards p28/truncated Rex inhibitors in HTLV-2. Conclusion Our data suggest a general converging pattern of expression of HTLV-2 and HTLV-1 and highlight peculiar differences in the expression of regulatory proteins that might influence the pathobiology of these viruses.

Details

Language :
English
ISSN :
17424690
Volume :
9
Issue :
1
Database :
Directory of Open Access Journals
Journal :
Retrovirology
Publication Type :
Academic Journal
Accession number :
edsdoj.f1c4d64df8284140b962887150e8b722
Document Type :
article
Full Text :
https://doi.org/10.1186/1742-4690-9-74