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Research Article

Mechanism of translation of monocistronic and multicistronic human immunodeficiency virus type 1 mRNAs.

S Schwartz, B K Felber, G N Pavlakis
S Schwartz
Human Retrovirus Section, National Cancer Institute-Frederick Cancer Research and Development Center, Maryland 21702-1201.
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B K Felber
Human Retrovirus Section, National Cancer Institute-Frederick Cancer Research and Development Center, Maryland 21702-1201.
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G N Pavlakis
Human Retrovirus Section, National Cancer Institute-Frederick Cancer Research and Development Center, Maryland 21702-1201.
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DOI: 10.1128/MCB.12.1.207
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ABSTRACT

We have used a panel of cDNA clones expressing wild-type and mutant human immunodeficiency virus type 1 (HIV-1) mRNAs to study translation of these mRNAs in eucaryotic cells. The tat open reading frame (ORF) has a strong signal for translation initiation, while rev and vpu ORFs have weaker signals. The expression of downstream ORFs is inhibited in mRNAs that contain the tat ORF as the first ORF. In contrast, downstream ORFs are expressed efficiently from mRNAs that have rev or vpu as the first ORF. All env mRNAs contain the upstream vpu ORF. Expression of HIV-1 Env protein requires a weak vpu AUG, which allows leaky scanning to occur, thereby allowing ribosomes access to the downstream env ORF. We concluded that HIV-1 mRNAs are translated by the scanning mechanism and that expression of more than one protein from each mRNA was caused by leaky scanning at the first AUG of the mRNA.

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Mechanism of translation of monocistronic and multicistronic human immunodeficiency virus type 1 mRNAs.
S Schwartz, B K Felber, G N Pavlakis
Molecular and Cellular Biology Jan 1992, 12 (1) 207-219; DOI: 10.1128/MCB.12.1.207

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Mechanism of translation of monocistronic and multicistronic human immunodeficiency virus type 1 mRNAs.
S Schwartz, B K Felber, G N Pavlakis
Molecular and Cellular Biology Jan 1992, 12 (1) 207-219; DOI: 10.1128/MCB.12.1.207
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