Frolov I, Schlesinger S
Department of Molecular Microbiology, Washington University, School of Medicine, St. Louis, Missouri 63110-1093, USA.
J Virol. 1996 Feb;70(2):1182-90. doi: 10.1128/JVI.70.2.1182-1190.1996.
Alphaviruses, particularly Sinbis virus and Semliki Forest virus, are proving to be useful vectors for the expression of heterologous genes. In infected cells, these self-replicating vectors (replicons) transcribe a subgenomic mRNA that codes for a heterologous protein instead of the structural proteins. We reported recently that translation of the reporter gene lacZ is enhanced 10-fold when the coding sequences of this gene are fused downstream of and in frame with the 5' half of the capsid gene (I. Frolov and S. Schlesinger, J. Virol. 68:8111-8117, 1994). The enhancing sequences, located downstream of the AUG codon that initiates translation of the capsid protein, have a predicted hairpin structure. We have mutated this region by making changes in the codons which do not affect the protein sequence but should destabilize the putative hairpin structure. These changes caused a decrease in the accumulation of the capsid-beta-galactosidase fusion protein. When these alterations were inserted into the capsid gene in the context of the intact Sindbis virus genome, they led to a decrease in the rate of virus formation but did not affect the final yield. We also altered the original sequence to one that has 12 contiguous G.C base pairs and should form a stable hairpin. The new sequence was essentially as effective as the original had been in enhancement of translation and in the rate of virus formation. The position of the predicted hairpin structure is important for its function; an insertion of 9 nucleotides or a deletion of 9 nucleotides decreased the level of translation. The insertion of a hairpin structure at a particular location downstream of the initiating AUG appears to be a way that alphaviruses have evolved to enhance translation of their mRNA, and, as a consequence, they produce high levels of the structural proteins which are needed for virus assembly. This high level of translation requires an intracellular environment in which host cell protein synthesis is inhibited.
甲病毒,尤其是辛德毕斯病毒和塞姆利基森林病毒,正被证明是用于表达异源基因的有用载体。在受感染的细胞中,这些自我复制载体(复制子)转录一种亚基因组mRNA,该mRNA编码一种异源蛋白而非结构蛋白。我们最近报道,当报告基因lacZ的编码序列与衣壳基因5'端的一半在下游融合且读框相同时,该基因的翻译增强了10倍(I. 弗罗洛夫和S. 施莱辛格,《病毒学杂志》68:8111 - 8117,1994)。增强序列位于启动衣壳蛋白翻译的AUG密码子下游,具有预测的发夹结构。我们通过改变密码子对该区域进行了突变,这些改变不影响蛋白质序列,但应会破坏假定的发夹结构的稳定性。这些变化导致衣壳 - β - 半乳糖苷酶融合蛋白的积累减少。当这些改变在完整的辛德毕斯病毒基因组背景下插入衣壳基因时,它们导致病毒形成速率降低,但不影响最终产量。我们还将原始序列改变为具有12个连续G.C碱基对且应形成稳定发夹的序列。新序列在增强翻译和病毒形成速率方面基本上与原始序列一样有效。预测的发夹结构的位置对其功能很重要;插入9个核苷酸或缺失9个核苷酸会降低翻译水平。在起始AUG下游的特定位置插入发夹结构似乎是甲病毒进化出的增强其mRNA翻译的一种方式,因此,它们产生高水平的病毒组装所需的结构蛋白。这种高水平的翻译需要宿主细胞蛋白质合成受到抑制的细胞内环境。