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Placeholder factors in ribosome biogenesis: please pave my way

机译:核糖体生物发生中的占位因子:请铺平道路

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摘要

The synthesis of cytoplasmic eukaryotic ribosomes is an extraordinarily energy-demanding cellular activity that occurs progressively from the nucleolus to the cytoplasm. In the nucleolus, precursor rRNAs associate with a myriad of trans-acting factors and some ribosomal proteins to form pre-ribosomal particles. These factors include snoRNPs, nucleases, ATPases, GTPases, RNA helicases, and a vast list of proteins with no predicted enzymatic activity. Their coordinate activity orchestrates in a spatiotemporal manner the modification and processing of precursor rRNAs, the rearrangement reactions required for the formation of productive RNA folding intermediates, the ordered assembly of the ribosomal proteins, and the export of pre-ribosomal particles to the cytoplasm; thus, providing speed, directionality and accuracy to the overall process of formation of translation-competent ribosomes. Here, we review a particular class of trans-acting factors known as "placeholders". Placeholder factors temporarily bind selected ribosomal sites until these have achieved a structural context that is appropriate for exchanging the placeholder with another site-specific binding factor. By this strategy, placeholders sterically prevent premature recruitment of subsequently binding factors, premature formation of structures, avoid possible folding traps, and act as molecular clocks that supervise the correct progression of pre-ribosomal particles into functional ribosomal subunits. We summarize the current understanding of those factors that delay the assembly of distinct ribosomal proteins or subsequently bind key sites in pre-ribosomal particles. We also discuss recurrent examples of RNA-protein and protein-protein mimicry between rRNAs and/or factors, which have clear functional implications for the ribosome biogenesis pathway.
机译:细胞质真核生物核糖体的合成是一种非常耗能的细胞活性,从核仁到细胞质逐渐发生。在核仁中,前体rRNA与无数反式作用因子和一些核糖体蛋白结合形成核糖体前颗粒。这些因素包括snoRNP,核酸酶,ATPase,GTPase,RNA解旋酶和大量蛋白质,这些蛋白质没有预期的酶促活性。它们的协调活性以时空方式协调前体rRNA的修饰和加工,形成有效的RNA折叠中间体所需的重排反应,核糖体蛋白的有序组装以及核糖体前颗粒向细胞质的输出;因此,为能翻译的核糖体形成的整个过程提供了速度,方向性和准确性。在这里,我们回顾一类特殊的交易因素,称为“占位符”。占位因子暂时结合选定的核糖体位点,直到它们达到了适合与其他位点特异性结合因子交换占位符的结构背景为止。通过这种策略,占位符在空间上阻止了随后结合因子的过早募集,结构的过早形成,避免了可能的折叠陷阱,并充当了监督前核糖体颗粒向功能性核糖体亚基正确发育的分子钟。我们总结了目前对延迟独特核糖体蛋白装配或随后结合核糖体前颗粒中关键位点的那些因素的理解。我们还讨论了rRNA和/或因子之间RNA-蛋白质和蛋白质-蛋白质模仿的重复实例,这些实例对核糖体生物发生途径具有明显的功能含义。

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