A minimal uORF within the HIV-1 vpu leader allows efficient translation initiation at the downstream env AUG

被引:38
作者
Krummheuer, Jorg
Johnson, Adam T.
Hauber, Ilona
Kammler, Susanne
Anderson, Jenny L.
Hauber, Joachim
Purcell, Damian F. J.
Schaal, Heiner
机构
[1] Univ Dusseldorf, Inst Virol, D-40225 Dusseldorf, Germany
[2] Univ Melbourne, Dept Microbiol & Immunol, Parkville, Vic 3010, Australia
[3] Heinrich Pette Inst Expt Virol & Immunol, D-20251 Hamburg, Germany
基金
英国医学研究理事会;
关键词
HIV; polycistronic mRNA; downstream translation; non-linear scanning; uORF;
D O I
10.1016/j.virol.2007.01.022
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The HIV-1 Vpu and Env proteins are translated from 16 alternatively spliced bicistronic mRNA isoforms. Translation of HIV-1 mRNAs generally follows the ribosome scanning mechanism. However, by using subgenomic env expression vectors, we found that translation of glycoprotein from polycistronic mRNAs was inconsistent with leaky scanning. Instead a conserved minimal upstream open reading frame (uORF) consisting only of a start and stop codon that overlaps with the vpu start site, appears to augment access to the em, start codon downstream. Mutating the translational start and stop codons of this uORF resulted in up to fivefold reduction in Env expression. Removing the vpu uORF and increasing the strength of the authentic vpu initiation sequence abolished Env expression from subgenomic constructs and replication of HIV-1, whereas an identical increase in the strength of the minimal uORF initiation site did not alter Env expression. (C) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:261 / 271
页数:11
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