| Autor: |
Buck CB; Program in Cellular and Molecular Medicine, Cellular and Molecular Biology, Baltimore, Maryland 21205, USA., Shen X, Egan MA, Pierson TC, Walker CM, Siliciano RF |
| Jazyk: |
angličtina |
| Zdroj: |
Journal of virology [J Virol] 2001 Jan; Vol. 75 (1), pp. 181-91. |
| DOI: |
10.1128/JVI.75.1.181-191.2001 |
| Abstrakt: |
Several retroviruses have recently been shown to promote translation of their gag gene products by internal ribosome entry. In this report, we show that mRNAs containing the human immunodeficiency virus type 1 (HIV-1) gag open reading frame (ORF) exhibit internal ribosome entry site (IRES) activity that can promote translational initiation of Pr55(gag). Remarkably, this IRES activity is driven by sequences within the gag ORF itself and is not dependent on the native gag 5'-untranslated region (UTR). This cap-independent mechanism for Pr55(gag) translation may help explain the high levels of translation of this protein in the face of major RNA structural barriers to scanning ribosomes found in the gag 5' UTR. The gag IRES activity described here also drives translation of a novel 40-kDa Gag isoform through translational initiation at an internal AUG codon found near the amino terminus of the Pr55(gag) capsid domain. Our findings suggest that this low-abundance Gag isoform may be important for wild-type replication of HIV-1 in cultured cells. The activities of the HIV-1 gag IRES may be an important feature of the HIV-1 life cycle and could serve as a novel target for antiretroviral therapeutic strategies. |
| Databáze: |
MEDLINE |
| Externí odkaz: |
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