Sample J, Liebowitz D, Kieff E
Department of Medicine, Harvard Medical School, Boston, Massachusetts 02115.
J Virol. 1989 Feb;63(2):933-7. doi: 10.1128/JVI.63.2.933-937.1989.
The structures of the 2.3- and 2.0-kilobase Epstein-Barr virus (EBV) mRNAs, partially encoded within the EcoRI J fragment DNA of the viral genome, were determined by analysis of their cDNAs. Both mRNAs are transcribed across the fused terminal repeats of the EBV episome and consist of nine exons. The mRNAs are transcribed from different promoters and have a unique 5' exon from the U5 region of the genome but eight common exons from the U1 region. One principal open reading frame is present in each mRNA and is predicted to encode 54,000- and 40,000-dalton integral membrane proteins. This result was confirmed by in vitro translation of RNAs in the presence of canine pancreatic microsomes. The 2.3-kilobase mRNA is not expressed in Raji cells, owing to the deletion of the 5' regulatory and coding region of this gene, whereas neither mRNA is expressed in Namalwa cells, owing to inactivation as a result of integration of the EBV genome via the terminal repeats. Since these mRNAs are readily detected in largely latently infected cells and do not increase in abundance with EBV replication, these putative latent-infection membrane proteins are tentatively designated LMP-2A and LMP-2B, respectively.
通过对其互补DNA(cDNA)的分析,确定了部分由病毒基因组的EcoRI J片段DNA编码的2.3千碱基和2.0千碱基爱泼斯坦-巴尔病毒(EBV)信使核糖核酸(mRNA)的结构。这两种mRNA均转录跨越EBV附加体的融合末端重复序列,由九个外显子组成。这些mRNA从不同的启动子转录而来,有一个来自基因组U5区域的独特5'外显子,但有八个来自U1区域的共同外显子。每个mRNA中都存在一个主要的开放阅读框,预计可编码54,000道尔顿和40,000道尔顿的整合膜蛋白。在犬胰腺微粒体存在的情况下对RNA进行体外翻译,证实了这一结果。2.3千碱基的mRNA在Raji细胞中不表达,这是由于该基因5'调控和编码区域的缺失,而两种mRNA在Namalwa细胞中均不表达,这是由于EBV基因组通过末端重复序列整合而失活所致。由于这些mRNA在大量潜伏感染的细胞中很容易被检测到,并且其丰度不会随着EBV复制而增加,因此这些假定的潜伏感染膜蛋白分别被暂定为LMP-2A和LMP-2B。