Sriram S, Gopinathan K P
Department of Microbiology and Cell Biology, Indian Institute of Science, Bangalore, 560 012, India.
Virology. 1998 Nov 10;251(1):108-22. doi: 10.1006/viro.1998.9404.
Several late gene expression factors (Lefs) have been implicated in fostering high levels of transcription from the very late gene promoters of polyhedrin and p10 from baculoviruses. We cloned and characterized from Bombyx mori nuclear polyhedrosis virus a late gene expression factor (Bmlef2) that encodes a 209-amino-acid protein harboring a Cys-rich C-terminal domain. The temporal transcription profiles of lef2 revealed a 1.2-kb transcript in both delayed early and late periods after virus infection. Transcription start site mapping identified the presence of an aphidicolin-sensitive late transcript arising from a TAAG motif located at -352 nucleotides and an aphidicolin-insensitive early transcript originating from a TTGT motif located 35 nucleotides downstream to a TATA box at -312 nucleotides, with respect to the +1 ATG of lef2. BmLef2 trans-activated very late gene expression from both polyhedrin and p10 promoters in transient expression assays. Internal deletion of the Cys-rich domain from the C-terminal region abolished the transcriptional activation. Inactivation of Lef2 synthesis by antisense lef2 transcripts drastically reduced the very late gene transcription but showed little effect on the expression from immediate early promoter. Decrease in viral DNA synthesis and a reduction in virus titer were observed only when antisense lef2 was expressed under the immediate early (ie-1) promoter. Furthermore, the antisense experiments suggested that lef2 plays a direct role in very late gene transcription.
几种晚期基因表达因子(Lefs)与促进杆状病毒多角体蛋白和p10极晚期基因启动子的高水平转录有关。我们从家蚕核型多角体病毒中克隆并鉴定了一种晚期基因表达因子(Bmlef2),它编码一种含有富含半胱氨酸的C末端结构域的209个氨基酸的蛋白质。lef2的瞬时转录谱显示,在病毒感染后的延迟早期和晚期均有一个1.2 kb的转录本。转录起始位点定位表明,存在一个由位于-352个核苷酸处的TAAG基序产生的对放线菌素D敏感的晚期转录本,以及一个由位于lef2的+1 ATG上游312个核苷酸处的TATA框下游35个核苷酸处的TTGT基序产生的对放线菌素D不敏感的早期转录本。在瞬时表达试验中,BmLef2反式激活了多角体蛋白和p10启动子的极晚期基因表达。从C末端区域内部删除富含半胱氨酸的结构域消除了转录激活。反义lef2转录本使Lef2合成失活,极大地降低了极晚期基因转录,但对立即早期启动子驱动的表达影响很小。仅当反义lef2在立即早期(ie-1)启动子控制下表达时,才观察到病毒DNA合成减少和病毒滴度降低。此外,反义实验表明lef2在极晚期基因转录中起直接作用。