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Assembly and functionality of the ribosome with tethered subunits

机译:带有束缚亚基的核糖体的组装和功能

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摘要

Ribo-T is an engineered ribosome whose small and large subunits are tethered together by linking 16S rRNA and 23S rRNA in a single molecule. Although Ribo-T can support cell proliferation in the absence of wild type ribosomes, Ribo-T cells grow slower than those with wild type ribosomes. Here, we show that cell growth defect is likely explained primarily by slow Ribo-T assembly rather than its imperfect functionality. Ribo-T maturation is stalled at a late assembly stage. Several post-transcriptional rRNA modifications and some ribosomal proteins are underrepresented in the accumulated assembly intermediates and rRNA ends are incompletely trimmed. Ribosome profiling of Ribo-T cells shows no defects in translation elongation but reveals somewhat higher occupancy by Ribo-T of the start codons and to a lesser extent stop codons, suggesting that subunit tethering mildly affects the initiation and termination stages of translation. Understanding limitations of Ribo-T system offers ways for its future development.
机译:Ribo-T是一种工程核糖体,其大小亚基通过将16S rRNA和23S rRNA连接在一个分子中而被束缚在一起。尽管在没有野生型核糖体的情况下,Ribo-T可以支持细胞增殖,但Ribo-T细胞的生长速度要比野生型核糖体的慢。在这里,我们表明细胞生长缺陷可能主要是由于Ribo-T组装缓慢而不是功能不完善所致。 Ribo-T的成熟在组装后期就停止了。转录后的一些rRNA修饰和一些核糖体蛋白在积累的组装中间体中含量不足,并且rRNA末端未完全修剪。 Ribo-T细胞的核糖体谱分析显示翻译延伸没有缺陷,但显示Ribo-T对起始密码子的占用率较高,而终止密码子的使用程度较小,这表明亚单位束缚会轻微影响翻译的起始和终止阶段。了解Ribo-T系统的局限性为其未来的发展提供了途径。

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