Ma C, Simons R W
Molecular Biology Institute, University of California, Los Angeles 90024.
EMBO J. 1990 Apr;9(4):1267-74. doi: 10.1002/j.1460-2075.1990.tb08235.x.
Transposase (tnp) expression from insertion sequence IS10 is controlled, in part, by an antisense RNA, RNA-OUT, which pairs to the translation initiation region of the tnp mRNA, RNA-IN. Genetic experiments suggest that control occurs post-transcriptionally. Here, we present evidence that bears on the control mechanism. Specific ribosome binding at the tnp translation initiation site is demonstrated in vitro. Two mutations that alter tnp translation in vivo are shown to have corresponding effects in vitro. Most importantly, RNA-OUT/RNA-IN pairing is shown to block ribosome binding. In conjunction with the work described in the accompanying paper, we propose that inhibition of ribosome binding also occurs in vivo, and that it is sufficient to account for control. Implications for translational control in analogous systems are discussed.
插入序列IS10的转座酶(tnp)表达部分受反义RNA即RNA-OUT的控制,RNA-OUT与tnp mRNA(RNA-IN)的翻译起始区域配对。遗传学实验表明这种控制发生在转录后。在此,我们提供了与控制机制相关的证据。体外实验证明了在tnp翻译起始位点存在特异性核糖体结合。体内改变tnp翻译的两个突变在体外显示出相应的效应。最重要的是,RNA-OUT/RNA-IN配对可阻断核糖体结合。结合随附论文中描述的工作,我们提出核糖体结合抑制在体内也会发生,并且这足以解释这种控制。文中还讨论了类似系统中翻译控制的意义。