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RNA 折叠和 RNA 解旋酶在核糖体生物发生中的功能。

RNA folding and functions of RNA helicases in ribosome biogenesis.

机构信息

Biochemistry Center, Heidelberg University, Im Neuenheimer Feld 328, Heidelberg, Germany.

BioTechMed-Graz, Graz, Austria.

出版信息

RNA Biol. 2022 Jan;19(1):781-810. doi: 10.1080/15476286.2022.2079890.

DOI:10.1080/15476286.2022.2079890
PMID:35678541
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9196750/
Abstract

Eukaryotic ribosome biogenesis involves the synthesis of ribosomal RNA (rRNA) and its stepwise folding into the unique structure present in mature ribosomes. rRNA folding starts already co-transcriptionally in the nucleolus and continues when pre-ribosomal particles further maturate in the nucleolus and upon their transit to the nucleoplasm and cytoplasm. While the approximate order of folding of rRNA subdomains is known, especially from cryo-EM structures of pre-ribosomal particles, the actual mechanisms of rRNA folding are less well understood. Both small nucleolar RNAs (snoRNAs) and proteins have been implicated in rRNA folding. snoRNAs hybridize to precursor rRNAs (pre-rRNAs) and thereby prevent premature folding of the respective rRNA elements. Ribosomal proteins (r-proteins) and ribosome assembly factors might have a similar function by binding to rRNA elements and preventing their premature folding. Besides that, a small group of ribosome assembly factors are thought to play a more active role in rRNA folding. In particular, multiple RNA helicases participate in individual ribosome assembly steps, where they are believed to coordinate RNA folding/unfolding events or the release of proteins from the rRNA. In this review, we summarize the current knowledge on mechanisms of RNA folding and on the specific function of the individual RNA helicases involved. As the yeast is the organism in which ribosome biogenesis and the role of RNA helicases in this process is best studied, we focused our review on insights from this model organism, but also make comparisons to other organisms where applicable.

摘要

真核生物核糖体生物发生涉及核糖体 RNA(rRNA)的合成及其逐步折叠成成熟核糖体中存在的独特结构。rRNA 折叠在核仁中已经在共转录过程中开始,并在 pre-ribosomal 颗粒在核仁中进一步成熟以及在它们向核质和细胞质转移时继续进行。虽然 rRNA 亚结构域的折叠大致顺序已知,特别是来自 pre-ribosomal 颗粒的 cryo-EM 结构,但 rRNA 折叠的实际机制了解较少。小核仁 RNA(snoRNA)和蛋白质都与 rRNA 折叠有关。snoRNA 与前体 rRNA(pre-rRNA)杂交,从而防止相应 rRNA 元件的过早折叠。核糖体蛋白(r-proteins)和核糖体组装因子可能通过与 rRNA 元件结合并防止其过早折叠而具有类似的功能。除此之外,一小部分核糖体组装因子被认为在 rRNA 折叠中发挥更积极的作用。在这篇综述中,我们总结了 RNA 折叠机制以及参与其中的特定 RNA 解旋酶的功能的最新知识。由于酵母是核糖体生物发生和 RNA 解旋酶在该过程中作用研究得最好的生物体,我们的综述重点关注了该模型生物的见解,但也在适用的情况下与其他生物体进行了比较。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a4fd/9196750/414573b7bec9/KRNB_A_2079890_F0005_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a4fd/9196750/90ea2ea483ca/KRNB_A_2079890_F0001_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a4fd/9196750/cea3f5b77313/KRNB_A_2079890_F0002_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a4fd/9196750/4e7837472724/KRNB_A_2079890_F0003_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a4fd/9196750/c8552ce747b9/KRNB_A_2079890_F0004_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a4fd/9196750/414573b7bec9/KRNB_A_2079890_F0005_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a4fd/9196750/90ea2ea483ca/KRNB_A_2079890_F0001_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a4fd/9196750/cea3f5b77313/KRNB_A_2079890_F0002_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a4fd/9196750/4e7837472724/KRNB_A_2079890_F0003_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a4fd/9196750/c8552ce747b9/KRNB_A_2079890_F0004_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a4fd/9196750/414573b7bec9/KRNB_A_2079890_F0005_OC.jpg

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