首页> 美国卫生研究院文献>Nucleic Acids Research >In polycistronic Qβ RNA single-strandedness at one ribosome binding site directly affects translational initiations at a distal upstream cistron
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In polycistronic Qβ RNA single-strandedness at one ribosome binding site directly affects translational initiations at a distal upstream cistron

机译:在多顺反子QβRNA中一个核糖体结合位点的单链直接影响远端顺反子在上游的翻译起始

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摘要

In Qβ RNA, sequestering the coat gene ribosome binding site in a putatively strong hairpin stem structure eliminated synthesis of coat protein and activated protein synthesis from the much weaker maturation gene initiation site, located 1300 nucleotides upstream. As the stability of a hairpin stem comprising the coat gene Shine–Dalgarno site was incrementally increased, there was a corresponding increase in translation of maturation protein. The effect of the downstream coat gene ribosome binding sequence on maturation gene expression appeared to have occurred only in cis and did not require an AUG start codon or initiation of coat protein synthesis. In all cases, no structural reorganization was predicted to occur within Qβ RNA. Our results suggest that protein synthesis from a relatively weak translational initiation site is greatly influenced by the presence or absence of a stronger ribosome binding site located elsewhere on the same RNA molecule. The data are consistent with a mechanism in which multiple ribosome binding sites compete in cis for translational initiations as a means of regulating protein synthesis on a polycistronic messenger RNA.
机译:在QβRNA中,将外壳基因的核糖体结合位点隔离在假定较强的发夹茎结构中,从而消除了外壳蛋白的合成,并从位于上游1300个核苷酸处的弱得多的成熟基因起始位点激活了蛋白质的合成。随着包含外壳基因Shine-Dalgarno位点的发夹茎的稳定性逐渐增加,成熟蛋白的翻译也相应增加。下游外壳基因核糖体结合序列对成熟基因表达的影响似乎仅在顺式中发生,并且不需要AUG起始密码子或外壳蛋白合成的起始。在所有情况下,预计在QβRNA中不会发生结构重组。我们的结果表明,来自相对弱的翻译起始位点的蛋白质合成受存在或不存在位于同一RNA分子其他位置的更强核糖体结合位点的极大影响。数据与其中多个核糖体结合位点在顺式竞争翻译起始的机制是一致的,该机制是调节多顺反子信使RNA上蛋白质合成的手段。

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