Rothstein D M, Bertonis J M
Biogen Research Corporation, Cambridge, MA 02142.
Gene. 1987;61(1):41-50. doi: 10.1016/0378-1119(87)90363-5.
Transcription along the human tissue-plasminogen activator gene (tpa) cloned in Escherichia coli was studied by inserting the 4.5S RNA gene at various locations within tpa, and measuring the accumulation of 4.5S RNA. A six-fold decrease in transcription of 4.5S RNA was observed as the distance from the Ptrc promoter to the 4.5S RNA gene increased. Independent measurements indicated that the quantity of initiations from the Ptrc promoter could not account for the differences observed. Because the 4.5S RNA is stable, the decrease in transcription was assumed to be due to premature transcription-termination within the tpa gene. This polar effect could contribute to poor expression of tpa in E. coli.
通过将4.5S RNA基因插入人组织纤溶酶原激活剂基因(tpa)内的不同位置,并测量4.5S RNA的积累,研究了克隆于大肠杆菌中的该基因的转录情况。随着从Ptrc启动子到4.5S RNA基因的距离增加,观察到4.5S RNA的转录下降了6倍。独立测量表明,Ptrc启动子的起始数量无法解释所观察到的差异。由于4.5S RNA是稳定的,转录下降被认为是由于tpa基因内的过早转录终止所致。这种极性效应可能导致tpa在大肠杆菌中的表达不佳。