多个控制元件参与SV40晚期转录的起始。

D C Rio, R Tjian
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引用次数: 0

摘要

在猴病毒40 (SV40)控制区缺失的突变体在HeLa细胞的核提取物中检测了其指导晚期转录的能力。引物延伸分析显示,SV40晚期转录主要在体外两个位点启动,其中一个位点对应于核苷酸325上的主要体内起始位点,另一个位点位于核苷酸170上。一系列的5',3'和内部缺失被用来定义两个不同的控制元件,它们似乎相互独立地起作用,并且位于每个体外起始位点的上游。此外,起始位点325的转录也受到在一个调控区域内发现的富含gc序列(CCGCCC)的影响,该区域由两个21 bp的完美重复序列和位于主要起始位点上游250 bp的第三个退化重复序列组成。这6个上游GC块位于起始位点170的上游,也影响起始位点的转录。虽然已知这些21 bp重复序列是SV40早期启动子的重要组成部分,但我们的研究结果表明,它们也参与调节体外晚期转录水平。
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Multiple control elements involved in the initiation of SV40 late transcription.

Mutants with deletions in the control region of simian virus 40 (SV40) were tested for their ability to direct late transcription in a nuclear extract derived from HeLa cells. Primer extension analysis revealed that late SV40 transcription initiates predominantly at two sites in vitro, one of which corresponds to the major in vivo start site at nucleotide 325, while the other site is located at nucleotide 170. A series of 5',3', and internal deletions of the putative promoter region were used to define two distinct control elements that appear to function independently of each other and that are located upstream from each of the in vitro initiation sites. In addition, transcription from the initiation site at 325 is also influenced by GC-rich sequences (CCGCCC) found within a regulatory region that consists of two 21 bp perfect repeats and a third degenerate repeat located 250 bp upstream from the major late initiation site. These six upstream GC blocks, which lie directly upstream from the initiation site at 170, also affect transcription from this start site. Although these 21 bp repeats are known to be an important part of the SV40 early promoter, our findings suggest that they are also involved in modulating the levels of late transcription in vitro.

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