| Literature DB >> 16916646 |
Susana T Valente1, Stephen P Goff.
Abstract
Cellular proteins are now appreciated as critically involved in all steps of the human immunodeficiency virus type 1 (HIV-1) life cycle, and disrupting host functions essential for virus replication may provide novel antiviral approaches. Selection from a human complementary DNA (cDNA) library for clones able to induce resistance to infection by recombinant HIV-1 genomes resulted in the identification of a gene fragment that potently restricts HIV-1 activity. The active cDNA encodes an N-terminal fragment of the heterogeneous nuclear ribonuclear protein U (hnRNP U). The gene fragment specifically targets the 3' long terminal repeat (3'LTR) in the viral mRNA and blocks the cytoplasmic accumulation of HIV-1 mRNAs. The results suggest that HIV-1 requires machinery for the nuclear export of viral mRNAs that can be specifically blocked by an interfering gene.Entities:
Mesh:
Substances:
Year: 2006 PMID: 16916646 DOI: 10.1016/j.molcel.2006.07.021
Source DB: PubMed Journal: Mol Cell ISSN: 1097-2765 Impact factor: 17.970