Ben-Asouli Y, Banai Y, Hauser H, Kaempfer R
Department of Molecular Virology, The Hebrew University-Hadassah Medical School, 91120 Jerusalem, Israel.
Nucleic Acids Res. 2000 Feb 15;28(4):1011-8. doi: 10.1093/nar/28.4.1011.
TAR, a 59 nt 5'-terminal hairpin in human immuno-deficiency virus 1 (HIV-1) mRNA, binds viral Tat and several cellular proteins. We report that eukaryotic translation initiation factor 2 (eIF2) recognizes TAR. TAR and the AUG initiation codon domain, located well downstream from TAR, both contribute to the affinity of HIV-1 mRNA for eIF2. The affinity of TAR for eIF2 was insensitive to lower stem mutations that modify sequence and structure or to sequence changes throughout the remainder that leave the TAR secondary structure intact. Hence, eIF2 recognizes structure rather than sequence in TAR. The affinity for eIF2 was severely reduced by a 3 nt change that converts the single A bulge into a 7 nt internal loop. T1 footprinting showed that eIF2 protects nucleotides in the loop as well as in the strand opposite the A bulge. Thus, eIF2 recognizes the TAR loop and lower part of the sub-apical stem. Though not contiguous, these regions are brought into proximity in TAR by a bend in the helical structure induced by the UCU bulge; binding of eIF2 opens up the bulge context and apical stem. The ability to bind eIF2 suggests a function for TAR in HIV-1 mRNA translation. Indeed, the 3 nt change that reduces the affinity of TAR for eIF2 impairs the ability of reporter mRNA to compete in translation. Interaction of TAR with eIF2 thus allows HIV-1 mRNA to compete more effectively during protein synthesis.
TAR是人类免疫缺陷病毒1(HIV-1)mRNA中一个59个核苷酸的5'末端发夹结构,它能结合病毒反式激活因子(Tat)和几种细胞蛋白。我们报告真核生物翻译起始因子2(eIF2)能识别TAR。TAR以及位于TAR下游较远位置的AUG起始密码子结构域,都对HIV-1 mRNA与eIF2的亲和力有贡献。TAR对eIF2的亲和力对改变序列和结构的下游茎部突变或对其余部分不改变TAR二级结构的序列变化不敏感。因此,eIF2识别的是TAR的结构而非序列。将单个A凸起转变为7个核苷酸的内部环的3个核苷酸变化会严重降低对eIF2的亲和力。T1足迹法显示eIF2保护环内以及与A凸起相对链上的核苷酸。因此,eIF2识别TAR环和近顶端茎的下部。尽管这些区域不相邻,但在TAR中,由UCU凸起诱导的螺旋结构弯曲使它们靠近;eIF2的结合会打开凸起区域和顶端茎。结合eIF2的能力表明TAR在HIV-1 mRNA翻译中具有功能。事实上,降低TAR对eIF2亲和力的3个核苷酸变化会损害报告基因mRNA在翻译中的竞争能力。TAR与eIF2的相互作用因此使HIV-1 mRNA在蛋白质合成过程中能更有效地竞争。