Matvienko N N, Zheleznaya L A, Chernyshova E E, Matvienko N I
Branch of Shemyakin-Ovchinnikov, Russian Academy of Sciences, Pushchino, Moscow Region, Russia.
Biochemistry (Mosc). 1997 Oct;62(10):1124-7.
The restriction-modification genes of the EcoRII system have been cloned into plasmids under control of phage-specific promoters T7 and SP6. The transcription was induced by cell infection with the recombinant M13 phages with the corresponding genes of phage RNA-polymerases under control of the Plac-promoter in the presence of IPTG. The induction yields significant amounts of EcoRII DNA-methylase for both phage-specific promoters. In both cases no increase in EcoRII endonuclease expression could be achieved. We hypothesize that the expression of the endonuclease gene is regulated on the translational level.
EcoRII系统的限制-修饰基因已被克隆到受噬菌体特异性启动子T7和SP6控制的质粒中。转录是通过在IPTG存在的情况下,用携带噬菌体RNA聚合酶相应基因且受Plac启动子控制的重组M13噬菌体感染细胞来诱导的。对于这两种噬菌体特异性启动子,诱导都产生了大量的EcoRII DNA甲基化酶。在这两种情况下,EcoRII内切核酸酶的表达都无法增加。我们推测内切核酸酶基因的表达是在翻译水平上受到调控的。