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Purα as a cellular co‐factor of Rev/RRE‐mediated expression of HIV‐1 intron‐containing mRNA
Author(s) -
Kaminski Rafal,
Darbinian Nune,
Sawaya Bassel E.,
Slonina Dorota,
Amini Shohreh,
Johnson Edward M.,
Rappaport Jay,
Khalili Kamel,
Darbinyan Armine
Publication year - 2007
Publication title -
journal of cellular biochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.028
H-Index - 165
eISSN - 1097-4644
pISSN - 0730-2312
DOI - 10.1002/jcb.21503
Subject(s) - rna , cytoplasm , nucleic acid , intron , rna binding protein , messenger rna , microbiology and biotechnology , biology , rna splicing , gene expression , chemistry , gene , genetics
To ensure successful replication, HIV‐1 has developed a Rev‐mediated RNA transport system that promotes the export of unspliced genomic RNA from nuclei to cytoplasm. This process requires the Rev responsive element (RRE) that is positioned in the viral transcript encoding Env protein, as well as in unspliced and singly spliced viral transcripts. We identified Purα, a single‐stranded nucleic acid binding protein as a cellular partner for Rev that augments the appearance of unspliced viral RNAs in the cytoplasm. A decrease in the level of Purα expression by siRNA diminishes the level of Rev‐dependent expression of viral RNA. Through its nucleic acid binding domain, Purα exhibits the ability to interact with the multimerization and RBD domains of Rev. Similar to Rev, Purα associates with RRE and in the presence of Rev forms a complex with slower electrophoretic mobility than those from Rev:RRE and Purα:RRE. The interaction of Purα with RRE occurs in the cytoplasm where enhanced association of Rev with RRE is observed. Our data indicate that the partnership of Purα with Rev is beneficial for Rev‐mediated expression of the HIV‐1 genome. J. Cell. Biochem. 103: 1231–1245, 2008. © 2007 Wiley‐Liss, Inc.