Abstract
Human immunodeficiency virus type 1 (HIV-1), like other lentiviruses, can infect non-dividing cells. The lentiviruses are most likely to have evolved a nuclear import strategy to import HIV-1 cDNA and viral protein complex through the nuclear pore complex (NPC) formed by nucleoporin proteins (Nup). In this study, we found that synthesis of integrated and 2LTR but not full-length form of HIV-1 cDNA was clearly impaired in culture via transduction of vesicular stomatitis virus matrix protein (VSV M), an inhibitor protein, through binding to the phenylalanine-glycine (FG) repeat region of Nup98. The impairment of synthesis of integrated and 2LTR DNA with VSV M was restored by ectopic overexpression of Nup98. A series of experiments using Nup98-depleted NPC by the small interfering RNA (siRNA) technique showed specific impairment of NPC structure and some functions, including nuclear import of HIV-1 cDNA. Our results suggest that Nup98 on the NPC specifically participates in the nuclear entry of HIV-1 cDNA following HIV-1 entry.
Original language | English |
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Pages (from-to) | 715-724 |
Number of pages | 10 |
Journal | Microbes and Infection |
Volume | 6 |
Issue number | 8 |
DOIs | |
Publication status | Published - 2004 Jul |
Externally published | Yes |
Keywords
- HIV-1
- NPC
- Nuclear import
- Nucleoporin
ASJC Scopus subject areas
- Microbiology
- Immunology
- Infectious Diseases