Literature DB >> 24243017

An unusual topological structure of the HIV-1 Rev response element.

Xianyang Fang1, Jinbu Wang, Ina P O'Carroll, Michelle Mitchell, Xiaobing Zuo, Yi Wang, Ping Yu, Yu Liu, Jason W Rausch, Marzena A Dyba, Jørgen Kjems, Charles D Schwieters, Soenke Seifert, Randall E Winans, Norman R Watts, Stephen J Stahl, Paul T Wingfield, R Andrew Byrd, Stuart F J Le Grice, Alan Rein, Yun-Xing Wang.   

Abstract

Nuclear export of unspliced and singly spliced viral mRNA is a critical step in the HIV life cycle. The structural basis by which the virus selects its own mRNA among more abundant host cellular RNAs for export has been a mystery for more than 25 years. Here, we describe an unusual topological structure that the virus uses to recognize its own mRNA. The viral Rev response element (RRE) adopts an "A"-like structure in which the two legs constitute two tracks of binding sites for the viral Rev protein and position the two primary known Rev-binding sites ~55 Å apart, matching the distance between the two RNA-binding motifs in the Rev dimer. Both the legs of the "A" and the separation between them are required for optimal RRE function. This structure accounts for the specificity of Rev for the RRE and thus the specific recognition of the viral RNA.
Copyright © 2013 Elsevier Inc. All rights reserved.

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Year:  2013        PMID: 24243017      PMCID: PMC3918456          DOI: 10.1016/j.cell.2013.10.008

Source DB:  PubMed          Journal:  Cell        ISSN: 0092-8674            Impact factor:   41.582


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