Department of Biochemistry and Molecular Biology, UMDNJ-New Jersey Medical School, and the Graduate School of Biomedical Sciences, Newark, NJ, USA.
RNA Biol. 2012 Oct;9(10):1255-65. doi: 10.4161/rna.21957. Epub 2012 Oct 1.
Polyadenylation is a 3' mRNA processing event that contributes to gene expression by affecting stability, export and translation of mRNA. Human polyadenylation signals (PAS) have core and auxiliary elements that bind polyadenylation factors upstream and downstream of the cleavage site. The majority of mRNAs do not have optimal upstream and downstream core elements and therefore auxiliary elements can aid in polyadenylation efficiency. Auxiliary elements have previously been identified and studied in a small number of mRNAs. We previously used a global approach to examine auxiliary elements to identify overrepresented motifs by a bioinformatic survey. This predicted information was used to direct our in vivo validation studies, all of which were accomplished using both a tandem in vivo polyadenylation assay and using reporter protein assays measured as luciferase activity. Novel auxiliary elements were placed in a test polyadenylation signal. An in vivo polyadenylation assay was used to determine the strength of the polyadenylation signal. All but one of the novel auxiliary elements enhanced the test polyadenylation signal. Effects of these novel auxiliary elements were also measured by a luciferase assay when placed in the 3' UTR of a firefly luciferase reporter. Two novel downstream auxiliary elements and all of the novel upstream auxiliary elements showed an increase in reporter protein levels. Many well known auxiliary polyadenylation elements have been found to occur in multiple sets. However, in our study, multiple copies of novel auxiliary elements brought reporter protein levels as well as polyadenylation choice back to wild type levels. Structural features of these novel auxiliary elements may also affect the role of auxiliary elements. A MS2 structure placed upstream of the polyadenylation signal can affect polyadenylation in both the positive and negative direction. A large change in RNA structure by using novel complementary auxiliary element also decreased polyadenylation choice and reporter protein levels. Therefore, we conclude that RNA structure has an important role in polyadenylation efficiency.
多聚腺苷酸化是一种 3' mRNA 加工事件,通过影响 mRNA 的稳定性、输出和翻译来促进基因表达。人类多聚腺苷酸化信号 (PAS) 具有核心和辅助元件,这些元件在切割位点的上下游结合多聚腺苷酸化因子。大多数 mRNA 没有最佳的上游和下游核心元件,因此辅助元件可以帮助提高多聚腺苷酸化效率。辅助元件已在少数 mRNA 中被鉴定和研究。我们之前使用全局方法检查辅助元件,通过生物信息学调查识别代表性基序。这些预测信息用于指导我们的体内验证研究,所有这些研究都是使用串联体内多聚腺苷酸化测定和报告蛋白测定(以荧光素酶活性衡量)完成的。将新的辅助元件放置在测试多聚腺苷酸化信号中。使用体内多聚腺苷酸化测定来确定多聚腺苷酸化信号的强度。除一个外,所有新的辅助元件都增强了测试多聚腺苷酸化信号。当将这些新的辅助元件放置在萤火虫荧光素酶报告基因的 3'UTR 中时,通过荧光素酶测定也测量了它们的作用。两个新的下游辅助元件和所有新的上游辅助元件都显示出报告蛋白水平的增加。许多众所周知的辅助多聚腺苷酸化元件已被发现存在于多组中。然而,在我们的研究中,新的辅助元件的多个副本使报告蛋白水平和多聚腺苷酸化选择恢复到野生型水平。这些新的辅助元件的结构特征也可能影响辅助元件的作用。MS2 结构放置在多聚腺苷酸化信号的上游可以影响正向和负向的多聚腺苷酸化。使用新的互补辅助元件的 RNA 结构的大变化也降低了多聚腺苷酸化选择和报告蛋白水平。因此,我们得出结论,RNA 结构在多聚腺苷酸化效率中起着重要作用。