Penn C R, Mahy B W
Virus Res. 1984 Jan;1(1):1-13. doi: 10.1016/0168-1702(84)90030-3.
Analogues of the mRNA 5'-terminal methyl cap structure were found to stimulate the influenza virion RNA-dependent RNA polymerase. The single nucleotide analogue m7GMP was incorporated into RNA during transcription in vitro, and the stimulatory effect was not additive with the primer ApG, suggesting that m7GMP stimulates the virion polymerase by priming virus-specific mRNA synthesis, as has been shown for ApG. By contrast, stimulation by m7G(5')ppp(5')m6AM2-O was additive with that by ApG, and we could not demonstrate incorporation of the similar analogue m7G(5')ppp(5')Am2-O into RNA during transcription. We propose that these dinucleotide cap analogues stimulate the virion polymerase by allosteric modulation, independent of priming. This stimulation can be abolished by mutation, without loss of other activities associated with the cap-dependent endonuclease.
人们发现,信使核糖核酸(mRNA)5'-末端甲基化帽结构的类似物能刺激流感病毒粒子的核糖核酸依赖的核糖核酸聚合酶。单核苷酸类似物m7GMP在体外转录过程中被掺入RNA,其刺激作用与引物ApG不存在相加效应,这表明m7GMP如同ApG那样,通过引发病毒特异性mRNA合成来刺激病毒粒子聚合酶。相比之下,m7G(5')ppp(5')m6AM2-O的刺激作用与ApG的刺激作用存在相加效应,而且我们无法证明在转录过程中类似物m7G(5')ppp(5')Am2-O能掺入RNA。我们提出,这些二核苷酸帽类似物通过变构调节来刺激病毒粒子聚合酶,而与引发作用无关。这种刺激作用可通过突变消除,同时不会丧失与帽依赖性核酸内切酶相关的其他活性。