Schek N, Cooke C, Alwine J C
Department of Microbiology, School of Medicine, University of Pennsylvania, Philadelphia 19104-6142.
Mol Cell Biol. 1992 Dec;12(12):5386-93. doi: 10.1128/mcb.12.12.5386-5393.1992.
The polyadenylation signal for the late mRNAs of simian virus 40 is known to have sequence elements located both upstream and downstream of the AAUAAA which affect efficiency of utilization of the signal. The upstream efficiency element has been previously characterized by using deletion mutations and transfection analyses. Those studies suggested that the upstream element lies between 13 and 48 nucleotides upstream of the AAUAAA. We have utilized in vitro cleavage and polyadenylation reactions to further define the upstream element. 32P-labeled substrate RNAs were prepared by in vitro transcription from wild-type templates as well as from mutant templates having deletions and linker substitutions in the upstream region. Analysis of these substrates defined the upstream region as sequences between 13 and 51 nucleotides upstream of the AAUAAA, in good agreement with the in vivo results. Within this region, three core elements with the consensus sequence AUUUGURA were identified and were specifically mutated by linker substitution. These core elements were found to contain the active components of the upstream efficiency element. Using substrates with both single and double linker substitution mutations of core elements, we observed that the core elements function in a distance-dependent manner. In mutants containing only one core element, the effect on efficiency increases as the distance between the element and the AAUAAA decreases. In addition, when core elements are present in multiple copies, the effect is additive. The core element consensus sequence, which bears homology to the Sm protein complex-binding site in human U1 RNA, is also found within the upstream elements of the ground squirrel hepatitis B and cauliflower mosaic virus polyadenylation signals (R. Russnak, Nucleic Acids Res. 19:6449-6456, 1991; H. Sanfacon, P. Brodmann, and T. Hohn, Genes Dev. 5:141-149, 1991), suggesting functional conservation of this element between mammals and plants.
已知猿猴病毒40晚期mRNA的聚腺苷酸化信号在AAUAAA的上游和下游都有影响该信号利用效率的序列元件。上游效率元件先前已通过缺失突变和转染分析进行了表征。这些研究表明,上游元件位于AAUAAA上游13至48个核苷酸之间。我们利用体外切割和聚腺苷酸化反应进一步确定上游元件。通过从野生型模板以及在上游区域具有缺失和接头取代的突变模板进行体外转录来制备32P标记的底物RNA。对这些底物的分析将上游区域定义为AAUAAA上游13至51个核苷酸之间的序列,与体内结果高度一致。在该区域内,鉴定出了三个具有共有序列AUUUGURA的核心元件,并通过接头取代对其进行了特异性突变。发现这些核心元件包含上游效率元件的活性成分。使用具有核心元件单接头和双接头取代突变的底物,我们观察到核心元件以距离依赖性方式发挥作用。在仅包含一个核心元件的突变体中,随着该元件与AAUAAA之间距离的减小,对效率的影响增加。此外,当核心元件以多个拷贝存在时,其作用是累加的。核心元件共有序列与人U1 RNA中的Sm蛋白复合物结合位点具有同源性,在松鼠肝炎B病毒和花椰菜花叶病毒聚腺苷酸化信号的上游元件中也发现了该序列(R. Russnak,《核酸研究》19:6449 - 6456,1991;H. Sanfacon,P. Brodmann和T. Hohn,《基因与发育》5:141 - 149,1991),这表明该元件在哺乳动物和植物之间具有功能保守性。