Chang P J, Chang Y S, Liu S T
Graduate Institute of Microbiology and Immunology, National Yang-Ming University, Shih-Pai, Taipei 112, Taiwan.
J Virol. 1998 Jun;72(6):5128-36. doi: 10.1128/JVI.72.6.5128-5136.1998.
The BZLF1 gene of Epstein-Barr virus (EBV), which encodes a transcription factor, Zta, is transcribed into monocistronic and bicistronic mRNAs from two different promoters during the immediate-early stage of the EBV lytic cycle. It is generally accepted that the Zta protein translated from the monocistronic mRNA profoundly influences the activation of the EBV lytic cycle. In this study, we constructed a plasmid, pCMV-RZLUC, which can transcribe a bicistronic mRNA consisting of BRLF1 and a BZLF1-luc fusion gene under latent conditions. P3HR1 cells transfected with this plasmid produce a luciferase activity which is approximately 17-fold higher than the activity exhibited by pRZLUC, a plasmid incapable of transcribing the bicistronic mRNA. Genetic analyses indicated that mutations in BRLF1 not only can decrease the translation of the fusion gene from the bicistronic mRNA but can also be complemented by a functional BRLF1 gene in cis. This observation implies that the product of BRLF1, Rta, is involved in the translation of the downstream gene. Results presented herein also demonstrate that these mutations cannot be complemented in trans with a plasmid overexpressing Rta, suggesting that the amount of Rta in the vicinity of the intercistronic region may be crucial for the translation. Furthermore, our results correspond to those of previous investigations indicating that the Zta protein can be translated from the bicistronic mRNA and that, similar to the translation of bicistronic ZLUC, mutations in BRLF1 also hinder the translation of Zta from the BRLF1-BZLF1 bicistronic mRNA. Translation of Zta from the bicistronic mRNA may play an essential role in the activation of the EBV lytic cycle.
爱泼斯坦-巴尔病毒(EBV)的BZLF1基因编码一种转录因子Zta,在EBV裂解周期的即刻早期阶段,该基因从两个不同的启动子转录为单顺反子和双顺反子mRNA。人们普遍认为,从单顺反子mRNA翻译而来的Zta蛋白对EBV裂解周期的激活有深远影响。在本研究中,我们构建了一个质粒pCMV-RZLUC,它能在潜伏条件下转录由BRLF1和BZLF1-荧光素酶融合基因组成的双顺反子mRNA。用该质粒转染的P3HR1细胞产生的荧光素酶活性比不能转录双顺反子mRNA的质粒pRZLUC所表现出的活性高约17倍。遗传学分析表明,BRLF1中的突变不仅会降低双顺反子mRNA中融合基因的翻译,而且在顺式中可被功能性BRLF1基因互补。这一观察结果表明,BRLF1的产物Rta参与下游基因的翻译。本文给出的结果还表明,这些突变不能被过表达Rta的质粒反式互补,这表明顺反子间区域附近的Rta量可能对翻译至关重要。此外,我们的结果与先前的研究结果一致,先前的研究表明Zta蛋白可从双顺反子mRNA翻译而来,并且与双顺反子ZLUC的翻译类似,BRLF1中的突变也会阻碍Zta从BRLF1-BZLF1双顺反子mRNA的翻译。从双顺反子mRNA翻译Zta可能在EBV裂解周期的激活中起重要作用。