酿酒酵母核仁小RNA与4,5-二磷酸磷脂酰肌醇结合。

IF 3.6 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Irma A Jiménez-Ramírez, Miguel A Uc-Chuc, Luis Carlos Rodríguez Zapata, Enrique Castaño
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引用次数: 0

摘要

背景:传统上,snoRNAs以其在转录后rRNA修饰中的引导作用而闻名。在此之前,我们的研究小组通过lirna -seq发现了几种可能与PIP2结合的rna。其中,snR191因其与该脂质潜在的特异性相互作用而脱颖而出,使其与其他snorna区别开来。然而,需要详细的研究来确定RNA和脂质之间的分子相互作用,这种相互作用仍然未知,但可能作为运输或液-液相分离的机制。这项研究旨在确定snR191和PIP2之间的相互作用。方法:建立RNA-PIP2相互作用的新方法。用pip2结合的硝化纤维素膜孵育酿酒酵母的总RNA并进行RT-PCR反应。我们通过分子对接和snoR191的硅基突变预测了snR191-PIP2的相互作用。结果:通过LIPRNA-seq分析,我们发现pip2结合的rna在多种生物过程中显著富集,包括跨膜运输和氧化还原功能。我们的RNA-PIP2相互作用方法是成功的。我们证明snR191在体外特异性地与PIP2相互作用。DNA的消除确保了相互作用测定是rna特异性的,加强了实验的稳健性。PIP2在茎-环-茎基序中与snR191对接。跨越4个核苷酸的6个氢键介导PIP2-snR191相互作用。最后,snR191的突变影响了结构折叠。结论:在本研究中,我们证明了一种测定rna -脂质相互作用的新方法的有效性,为snR191和PIP2之间的特异性相互作用提供了强有力的证据。结合生物化学和计算方法使我们能够理解这些生物分子的结合。因此,这项工作大大拓宽了我们对snR191-PIP2相互作用的理解,并为进一步的研究开辟了新的视角。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Small Nucleolar RNA from <i>S. cerevisiae</i> Binds to Phosphatidylinositol 4,5-Bisphosphate.

Small Nucleolar RNA from <i>S. cerevisiae</i> Binds to Phosphatidylinositol 4,5-Bisphosphate.

Small Nucleolar RNA from <i>S. cerevisiae</i> Binds to Phosphatidylinositol 4,5-Bisphosphate.

Small Nucleolar RNA from S. cerevisiae Binds to Phosphatidylinositol 4,5-Bisphosphate.

Background: snoRNAs have traditionally been known for their role as guides in post-transcriptional rRNA modifications. Previously, our research group identified several RNAs that may bind to PIP2 with LIPRNA-seq. Among them, snR191 stood out due to its potential specific interaction with this lipid, distinguishing itself from other snoRNAs. However, a detailed study is needed to define the molecular interactions between RNA and lipids, which remain unknown but may serve as a mechanism for transport or liquid-liquid phase separation. This study aimed to determine the interaction between a snoRNA called snR191 and PIP2. Method: A novel methodology for RNA-PIP2 interaction was carried out. Total RNA from Saccharomyces cerevisiae was incubated with PIP2-bound nitrocellulose membranes and RT-PCR reactions. We performed the prediction of snR191-PIP2 interaction by molecular docking and in silico mutations of snoR191. Results: From LIPRNA-seq analysis, we identified that PIP2-bound RNAs were significantly enriched in diverse biological processes, including transmembrane transport and redox functions. Our RNA-PIP2 interaction approach was successful. We demonstrated that snR191 specifically interacts with PIP2 in vitro. The elimination of DNA ensured that the interaction assay was RNA-specific, strengthening the robustness of the experiment. PIP2 was docked to snR191 in a stem-loop-stem motif. Six hydrogen bonds across four nucleotides mediated the PIP2-snR191 interaction. Finally, mutations in snR191 affected the structural folding. Conclusions: In this study, we demonstrate the effectiveness of a new methodology for determining RNA-lipid interactions, providing strong evidence for the specific interaction between snR191 and PIP2. Integrating biochemical and computational approaches has allowed us to understand the binding of these biomolecules. Therefore, this work significantly broadens our understanding of snR191-PIP2 interactions and opens new perspectives for further research.

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来源期刊
Non-Coding RNA
Non-Coding RNA Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
6.70
自引率
4.70%
发文量
74
审稿时长
10 weeks
期刊介绍: Functional studies dealing with identification, structure-function relationships or biological activity of: small regulatory RNAs (miRNAs, siRNAs and piRNAs) associated with the RNA interference pathway small nuclear RNAs, small nucleolar and tRNAs derived small RNAs other types of small RNAs, such as those associated with splice junctions and transcription start sites long non-coding RNAs, including antisense RNAs, long ''intergenic'' RNAs, intronic RNAs and ''enhancer'' RNAs other classes of RNAs such as vault RNAs, scaRNAs, circular RNAs, 7SL RNAs, telomeric and centromeric RNAs regulatory functions of mRNAs and UTR-derived RNAs catalytic and allosteric (riboswitch) RNAs viral, transposon and repeat-derived RNAs bacterial regulatory RNAs, including CRISPR RNAS Analysis of RNA processing, RNA binding proteins, RNA signaling and RNA interaction pathways: DICER AGO, PIWI and PIWI-like proteins other classes of RNA binding and RNA transport proteins RNA interactions with chromatin-modifying complexes RNA interactions with DNA and other RNAs the role of RNA in the formation and function of specialized subnuclear organelles and other aspects of cell biology intercellular and intergenerational RNA signaling RNA processing structure-function relationships in RNA complexes RNA analyses, informatics, tools and technologies: transcriptomic analyses and technologies development of tools and technologies for RNA biology and therapeutics Translational studies involving long and short non-coding RNAs: identification of biomarkers development of new therapies involving microRNAs and other ncRNAs clinical studies involving microRNAs and other ncRNAs.
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