Arrand J R, Rymo L
J Virol. 1982 Feb;41(2):376-89. doi: 10.1128/JVI.41.2.376-389.1982.
Cytoplasmic RNA prepared from five lymphoid cell lines and a Burkitt lymphoma biopsy was radioactively labeled in vitro and hybridized to cloned EcoRI restriction endonuclease fragments of B95-8 Epstein-Barr virus DNA. The results confirmed that the most abundant cytoplasmic RNA species in such cells is specified by a small region of the genome defined by the EcoRI J fragment. Detailed mapping experiments precisely localized these transcripts within the sequence of the rightmost one-third of the EcoRI J fragment. DNA sequencing suggested that this region of the Epstein-Barr virus genome is unable to code for protein. The major early transcripts consisted of two non-polyadenylated RNA species, each about 170 nucleotides in length. They were both transcribed off the same strand of the DNA and showed significant sequence homology with each other. The coding sequences of the two small RNAs contained potential intragenic control regions for RNA polymerase III.
从五个淋巴样细胞系和一份伯基特淋巴瘤活检组织制备的细胞质RNA在体外进行放射性标记,并与B95 - 8爱泼斯坦-巴尔病毒DNA的克隆EcoRI限制性内切酶片段杂交。结果证实,此类细胞中最丰富的细胞质RNA种类由EcoRI J片段定义的基因组小区域所指定。详细的图谱实验将这些转录本精确地定位在EcoRI J片段最右侧三分之一的序列内。DNA测序表明,爱泼斯坦-巴尔病毒基因组的该区域无法编码蛋白质。主要的早期转录本由两种非多聚腺苷酸化的RNA种类组成,每种长度约为170个核苷酸。它们都从DNA的同一条链转录而来,并且彼此显示出显著的序列同源性。这两种小RNA的编码序列包含RNA聚合酶III的潜在基因内控制区域。