Majerciak Vladimir, Zheng Zhi-Ming
Tumor Virus RNA Biology Section, Gene Regulation and Chromosome Biology Laboratory, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Frederick, 21702 MD, USA.
Tumor Virus RNA Biology Section, Gene Regulation and Chromosome Biology Laboratory, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Frederick, 21702 MD, USA.
Virology. 2016 Jan 15;488:81-7. doi: 10.1016/j.virol.2015.10.031. Epub 2015 Nov 21.
In lytically infected B cells Kaposi sarcoma-associated herpesvirus (KSHV) ORF57 gene encodes two RNA isoforms by alternative splicing of its pre-mRNA, which contains a small, constitutive intron in its 5' half and a large, suboptimal intron in its 3's half. The RNA1 isoform encodes full-length ORF57 and is a major isoform derived from splicing of the constitutive small intron, but retaining the suboptimal large intron as the coding region. A small fraction (<5%) of ORF57 RNA undergoes double splicing to produce a smaller non-coding RNA2 due to lack of a translational termination codon. Both RNAs are cleaved and polyadenylated at the same cleavage site CS83636. The insertion of ORF57 RNA1 into a restriction cutting site in certain mammalian expression vectors activates splicing of the subopitmal intron and produces a truncated ORF57 protein.
在被裂解感染的B细胞中,卡波西肉瘤相关疱疹病毒(KSHV)的ORF57基因通过其前体mRNA的可变剪接编码两种RNA异构体,该前体mRNA在其5'端一半含有一个小的组成型内含子,在其3'端一半含有一个大的、次优的内含子。RNA1异构体编码全长ORF57,是源自组成型小内含子剪接的主要异构体,但保留次优大内含子作为编码区。由于缺乏翻译终止密码子,一小部分(<5%)的ORF57 RNA会进行双重剪接以产生较小的非编码RNA2。两种RNA都在相同的切割位点CS83636处被切割并聚腺苷酸化。将ORF57 RNA1插入某些哺乳动物表达载体中的限制性切割位点会激活次优内含子的剪接并产生截短的ORF57蛋白。