Kern F G, Bovi P D, Basilico C
Department of Pathology, New York University School of Medicine, New York 10016.
J Virol. 1987 Dec;61(12):4055-9. doi: 10.1128/JVI.61.12.4055-4059.1987.
In cells transformed by polyomavirus, the viral genome is integrated into the host DNA, and in the absence of excision, viral gene expression is limited to the early region. We report here that the ability of a unique transformed rat cell line, designated SS1A, to produce readily detectable levels of late mRNAs is due to rearrangements of the integrated viral sequences. The structure of the SS1A insertion, resulting from amplification and deletion events, allows for the formation of a primary late transcript that can subsequently be spliced to generate a reiterated leader attached to the body of the late mRNA coding sequences. The presence of transcripts containing such a leader was confirmed by sequencing the 5' end of cDNA copies of late mRNAs isolated from a library constructed with SS1A mRNA. These results suggest that a reiterated leader sequence is necessary to stabilize late mRNA.
在多瘤病毒转化的细胞中,病毒基因组整合到宿主DNA中,并且在没有切除的情况下,病毒基因表达仅限于早期区域。我们在此报告,一种独特的转化大鼠细胞系(命名为SS1A)能够产生易于检测到的晚期mRNA水平,这是由于整合的病毒序列发生了重排。由扩增和缺失事件导致的SS1A插入结构允许形成初级晚期转录本,随后该转录本可以被剪接以产生连接到晚期mRNA编码序列主体的重复前导序列。通过对从用SS1A mRNA构建的文库中分离的晚期mRNA的cDNA拷贝的5'末端进行测序,证实了含有这种前导序列的转录本的存在。这些结果表明,重复的前导序列对于稳定晚期mRNA是必要的。