Whitton J L, Clements J B
Nucleic Acids Res. 1984 Feb 24;12(4):2061-79. doi: 10.1093/nar/12.4.2061.
We have determined the structure of the 5' portion of herpes simplex virus type 2 (HSF-2) immediate-early (IE) mRNA-3 and have obtained the DNA sequence specifying the N terminus of its encoded polypeptide, Vmw182, its untranslated leader and the intergenic region between IEmRNAs-3 & 4/5. Comparison of the HSV-2 intergenic sequences with the HSV-1 equivalent region identifies several conserved regions: (1) an AT-rich element with core consensus TAATGARAT which is likely to be the 'activator' sequence through which coordinate induction of the IE gene family is mediated. (2) GC-rich and GA-rich tracts, found in a wide variety of eukaryotic promoters, which vary in position and orientation between HSV-2 and HSV-1 and which represent modulators of transcription. (3) TATA homologies present 15-25 base pairs (bp) upstream of mRNA 5' termini. (4) a 137bp direct repeat in HSV-2 which contains sequence almost identical to the HSV-1 replication origin.
我们已经确定了单纯疱疹病毒2型(HSV-2)立即早期(IE)mRNA-3 5'端的结构,并获得了指定其编码多肽Vmw182的N端、其非翻译前导序列以及IEmRNAs-3与4/5之间基因间隔区的DNA序列。将HSV-2基因间隔序列与HSV-1的等效区域进行比较,确定了几个保守区域:(1)一个富含AT的元件,其核心共有序列为TAATGARAT,它可能是介导IE基因家族协同诱导的“激活子”序列。(2)富含GC和富含GA的片段,存在于多种真核启动子中,在HSV-2和HSV-1之间的位置和方向不同,它们代表转录调节因子。(3)在mRNA 5'端上游15-25个碱基对(bp)处存在TATA同源序列。(4)HSV-2中的一个137bp直接重复序列,其包含与HSV-1复制起点几乎相同的序列。