Author/Authors :
Xianyang Fang، نويسنده , , Jinbu Wang، نويسنده , , Ina P. O’Carroll، نويسنده , , Michelle Mitchell، نويسنده , , Xiaobing Zuo، نويسنده , , Yi Wang، نويسنده , , Ping Yu، نويسنده , , Yu Liu، نويسنده , , Jason W. Rausch، نويسنده , , Marzena A. Dyba، نويسنده , , J?rgen Kjems، نويسنده , , Charles D. Schwieters، نويسنده , , Soenke Seifert، نويسنده , , Randall E. Winans، نويسنده , , Norman R. Watts، نويسنده , , Stephen J. Stahl، نويسنده , , Paul T. Wingfield، نويسنده , , R. Andrew Byrd، نويسنده , , Stuart F.J. Le Grice، نويسنده , , Alan Rein، نويسنده , , et al.، نويسنده ,
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.
