Wong E M, Polisky B
Cell. 1985 Oct;42(3):959-66. doi: 10.1016/0092-8674(85)90292-2.
Replication of the ColE1 plasmid is regulated by the interaction of its primer RNA with a small countertranscript (RNA I) that acts as a repressor of functional primer formation. The interaction is dependent on the specific conformations of the complementary RNA molecules. Early in its synthesis, primer adopts an "anti-RNA I" configuration. As transcription proceeds, it is preempted by formation of an alternative domain designated stem-loop IV. This conformational transition has a significant effect on the rate of association of RNA I with the primer in vitro. Nascent primer in the "anti-RNA I" conformation (135 nucleotides) interacts with RNA I 6-fold faster than primer in the stem-loop IV conformation (241 nucleotides), and 35-fold faster than a 567 nucleotide primer precursor. We propose that a conformation-dependent "window of susceptibility" of primer to RNA I exists during primer transcription, and that altered conformations play a role in modulating the rate of functional primer formation.
ColE1质粒的复制受其引物RNA与一种小反式转录本(RNA I)相互作用的调控,RNA I作为功能性引物形成的阻遏物。这种相互作用取决于互补RNA分子的特定构象。在引物合成早期,引物采用“抗RNA I”构象。随着转录的进行,它会被一个称为茎环IV的替代结构域的形成所取代。这种构象转变对RNA I与引物在体外的结合速率有显著影响。处于“抗RNA I”构象的新生引物(135个核苷酸)与RNA I相互作用的速度比处于茎环IV构象的引物(241个核苷酸)快6倍,比567个核苷酸的引物前体快35倍。我们提出,在引物转录过程中存在引物对RNA I的构象依赖性“敏感窗口”,并且改变的构象在调节功能性引物形成的速率中起作用。