Blumenthal T
Proc Natl Acad Sci U S A. 1980 May;77(5):2601-5. doi: 10.1073/pnas.77.5.2601.
Qbeta replicase is notable for its high degree of template specificity. It has been shown to transcribe Qbeta RNA and synthetic polymers containing cytidylate. However, other natural RNAs are not transcribed unless Mn2+ ions are present. The enzyme initiates all RNA synthesis with GTP. In this report it is shown that Qbeta replicase can transcribe heterologous natural RNA species in the absence of Mn2+ if sufficient GTP is present. Each RNA tested requires a different GTP concentration for initiation. These results indicate that the site for the initiating nucleoside triphosphate on Qbeta replicase is strongly influenced by the template. It is proposed that the high degree of template specificity is a consequence of the fact that different templates induce initiation sites with varying affinities for GTP. Two lines of evidence support this idea. First, Mn2+ ions, which reduce template specificity, reduce the concentration of GTP required for initiation. Second, high ionic strength, which decreases transcription of all templates except Qbeta RNA, increases the GTP requirement. The possibility is considered that variable promoter or ribosome binding site strengths could result from a mechanism similar to that proposed here.
Qβ复制酶以其高度的模板特异性而闻名。已证明它能转录Qβ RNA和含有胞苷酸的合成聚合物。然而,除非存在锰离子,否则其他天然RNA不会被转录。该酶以鸟苷三磷酸(GTP)启动所有RNA合成。本报告表明,如果存在足够的GTP,Qβ复制酶在不存在锰离子的情况下可以转录异源天然RNA种类。每种测试的RNA起始都需要不同的GTP浓度。这些结果表明,Qβ复制酶上起始核苷三磷酸的位点受到模板的强烈影响。有人提出,高度的模板特异性是不同模板诱导对GTP具有不同亲和力的起始位点这一事实的结果。有两条证据支持这一观点。首先,降低模板特异性的锰离子会降低起始所需的GTP浓度。其次,高离子强度会降低除Qβ RNA外所有模板的转录,但会增加对GTP的需求。人们考虑了可变启动子或核糖体结合位点强度可能由类似于本文提出的机制导致的可能性。