Laboratory of Plant Molecular Biology, The Rockefeller University, 1230 York Avenue, 10021, New York, NY, U.S.A..
Plant Mol Biol. 1987 Jan;8(1):23-35. doi: 10.1007/BF00016431.
We have introduced chimeric genes containing polyadenylation signals from a human gene and two animal virus genes into tobacco cells. We see, in all three cases, inefficient and 'aberrant' utilization of the foreign polyadenylation signals. We find that a chimeric gene carrying the polyadenylation site of the human growth hormone gene is polyadenylated at three sites in the vicinity of the site that is polyadenylated in human cells. A chimeric gene containing the polyadenylation site from the adenovirus 5 E1A gene is polyadenylated at a site 11 bases downstream from that reported in animal cells. A gene carrying the polyadenylation site from the SV40 early region is polyadenylated some 80 bases upstream from the site that is polyadenylated in animal cells. In all three cases, related mRNAs ending at flanking 'authentic' plant polyadenylation sites can be detected, indicating that the foreign polyadenylation signals are inefficiently utilized in tobacco cells.
我们已将含有人类基因和两种动物病毒基因的多聚腺苷酸化信号的嵌合基因导入烟草细胞。在这三种情况下,我们都观察到外源多聚腺苷酸化信号的利用效率低下和“异常”。我们发现,携带人类生长激素基因多聚腺苷酸化位点的嵌合基因在靠近人类细胞中多聚腺苷酸化位点的三个位点处进行多聚腺苷酸化。含有来自腺病毒 5 E1A 基因的多聚腺苷酸化位点的嵌合基因在距动物细胞报道的位点 11 个碱基下游的位点处进行多聚腺苷酸化。携带 SV40 早期区多聚腺苷酸化位点的基因在距动物细胞中多聚腺苷酸化位点上游约 80 个碱基的位点处进行多聚腺苷酸化。在所有三种情况下,都可以检测到末端位于侧翼“真实”植物多聚腺苷酸化位点的相关 mRNA,表明外源多聚腺苷酸化信号在烟草细胞中的利用效率低下。