Chiou H C, Dabrowski C, Alwine J C
Department of Microbiology, School of Medicine, University of Pennsylvania, Philadelphia 19104-6148.
J Virol. 1991 Dec;65(12):6677-85. doi: 10.1128/JVI.65.12.6677-6685.1991.
We have examined the contribution of 5' leader sequences to expression directed by the simian virus 40 (SV40) late promoter. These studies showed that addition of sequences which contain the late leader 3' splice site to the late promoter led to an increase in the accumulation of mRNA expressed by the promoter. No other sequences within the leader region, between SV40 positions 334 and 560, exhibited a substantial influence on mRNA accumulation. The increase was due, at least in part, to the creation of a spliceable mRNA transcript, since mutation of either the 5' or 3' splice site could attenuate the effect. However, sequences at or near the 3' splice site appeared to play a more important role than did the 5' splice site in bringing about this increase. In many instances, mutation of the 3' splice site also led to the accumulation of extended transcripts, whereas mutation of the 5' splice site did not produce this result in any instance. Analysis of these extended transcripts showed that they retained sequences normally lost upon cleavage and polyadenylation. This finding suggested that mutation of the 3' splice site sequence led to decreases in the efficiency of polyadenylation. We propose that the SV40 late leader sequences positively contribute to expression of the viral late genes by increasing mRNA accumulation via multiple mechanisms, including the enhancement of pre-mRNA polyadenylation efficiency.
我们研究了5'前导序列对猿猴病毒40(SV40)晚期启动子指导的基因表达的贡献。这些研究表明,将包含晚期前导序列3'剪接位点的序列添加到晚期启动子上,会导致该启动子所表达的mRNA积累增加。在SV40的334至560位之间的前导区域内,没有其他序列对mRNA积累表现出实质性影响。这种增加至少部分归因于可剪接的mRNA转录本的产生,因为5'或3'剪接位点的突变均可减弱这种效应。然而,在实现这种增加方面,3'剪接位点处或其附近的序列似乎比5'剪接位点发挥着更重要的作用。在许多情况下,3'剪接位点的突变还导致了延伸转录本的积累,而5'剪接位点的突变在任何情况下都不会产生这种结果。对这些延伸转录本的分析表明,它们保留了在切割和聚腺苷酸化时通常会丢失的序列。这一发现表明,3'剪接位点序列的突变导致聚腺苷酸化效率降低。我们提出,SV40晚期前导序列通过多种机制增加mRNA积累,包括提高前体mRNA聚腺苷酸化效率,从而对病毒晚期基因的表达产生积极贡献。