| Literature DB >> 10860744 |
O K Haffar1, S Popov, L Dubrovsky, I Agostini, H Tang, T Pushkarsky, S G Nadler, M Bukrinsky.
Abstract
Replication of HIV-1 in non-dividing and slowly proliferating cell populations depends on active import of the viral pre-integration complex (PIC) into the cell nucleus. While it is commonly accepted that this process is mediated by an interaction between the HIV-1 PIC and the cellular nuclear import machinery, controversial results have been reported concerning the mechanisms of this interaction. Here, we demonstrate that a recently identified nuclear localization signal within the HIV-1 matrix protein (MA), MA NLS-2, together with previously described MA NLS-1, mediates nuclear import of the HIV-1 PIC. Inactivation of both MA NLSs precluded nuclear translocation of MA and rendered the virus defective in nuclear import and replication in non-dividing macrophage cultures, even when functional Vpr and integrase (IN), two more viral proteins implicated in HIV-1 nuclear import, were present. Taken together, these results indicate that Vpr does not function as an independent nuclear import factor and demonstrate that HIV-1 MA, by virtue of its two nuclear localization signals, regulates HIV-1 nuclear import. Copyright 2000 Academic Press.Entities:
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Year: 2000 PMID: 10860744 DOI: 10.1006/jmbi.2000.3768
Source DB: PubMed Journal: J Mol Biol ISSN: 0022-2836 Impact factor: 5.469