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涉及 snoRNAs 和 Rok1 解旋酶的核糖体前 RNA 相互作用网络。

A pre-ribosomal RNA interaction network involving snoRNAs and the Rok1 helicase.

机构信息

Centre for Biochemistry and Molecular Cell Biology, Georg-August-University, 37073 Göttingen, Germany.

Institute for Molecular Biosciences, Goethe University, 60438 Frankfurt, Germany.

出版信息

RNA. 2014 Aug;20(8):1173-82. doi: 10.1261/rna.044669.114. Epub 2014 Jun 19.

Abstract

Ribosome biogenesis in yeast requires 75 small nucleolar RNAs (snoRNAs) and a myriad of cofactors for processing, modification, and folding of the ribosomal RNAs (rRNAs). For the 19 RNA helicases implicated in ribosome synthesis, their sites of action and molecular functions have largely remained unknown. Here, we have used UV cross-linking and analysis of cDNA (CRAC) to reveal the pre-rRNA binding sites of the RNA helicase Rok1, which is involved in early small subunit biogenesis. Several contact sites were identified in the 18S rRNA sequence, which interestingly all cluster in the "foot" region of the small ribosomal subunit. These include a major binding site in the eukaryotic expansion segment ES6, where Rok1 is required for release of the snR30 snoRNA. Rok1 directly contacts snR30 and other snoRNAs required for pre-rRNA processing. Using cross-linking, ligation and sequencing of hybrids (CLASH) we identified several novel pre-rRNA base-pairing sites for the snoRNAs snR30, snR10, U3, and U14, which cluster in the expansion segments of the 18S rRNA. Our data suggest that these snoRNAs bridge interactions between the expansion segments, thereby forming an extensive interaction network that likely promotes pre-rRNA maturation and folding in early pre-ribosomal complexes and establishes long-range rRNA interactions during ribosome synthesis.

摘要

酵母核糖体生物发生需要 75 种小核仁 RNA(snoRNA)和无数的辅助因子,用于 rRNA(核糖体 RNA)的加工、修饰和折叠。对于涉及核糖体合成的 19 种 RNA 解旋酶,其作用部位和分子功能在很大程度上仍然未知。在这里,我们使用 UV 交联和 cDNA(CRAC)分析来揭示参与早期小亚基生物发生的 RNA 解旋酶 Rok1 的 pre-rRNA 结合位点。在 18S rRNA 序列中鉴定了几个接触位点,这些位点有趣地都聚集在小核糖体亚基的“脚”区域。其中包括在真核扩展片段 ES6 中的一个主要结合位点,Rok1 在 snR30 snoRNA 的释放中是必需的。Rok1 直接与 snR30 和其他 snoRNAs 接触,这些 snoRNAs 是 pre-rRNA 加工所必需的。使用交联、连接和杂交测序(CLASH),我们鉴定了 snoRNAs snR30、snR10、U3 和 U14 的几个新的 pre-rRNA 碱基配对位点,它们聚集在 18S rRNA 的扩展片段中。我们的数据表明,这些 snoRNAs 桥接了扩展片段之间的相互作用,从而形成了一个广泛的相互作用网络,可能促进早期前核糖体复合物中 pre-rRNA 的成熟和折叠,并在核糖体合成过程中建立 rRNA 的长程相互作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a2e/4105744/5e5b77858f20/1173f01.jpg

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