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Small-molecule affinity capture of DNA/RNA quadruplexes and their identification in vitro and in vivo through the G4RP protocol

机译:通过G4RP协议在体外和体内鉴定DNA / RNA QuadrupleS的小分子亲和力捕获及其鉴定

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摘要

Guanine-rich DNA and RNA sequences can fold into higher-order structures known as G-quadruplexes (or G4-DNA and G4-RNA, respectively). The prevalence of the G4 landscapes in the human genome, transcriptome and ncRNAome (non-coding RNA), collectively known as G4ome, is strongly suggestive of biological relevance at multiple levels (gene expression, replication). Small-molecules can be used to track G4s in living cells for the functional characterization of G4s in both normal and disease-associated changes in cell biology. Here, we describe biotinylated biomimetic ligands referred to as BioTASQ and their use as molecular tools that allow for isolating G4s through affinity pull-down protocols. We demonstrate the general applicability of the method by purifying biologically relevant G4s from nucleic acid mixtures in vitro and from human cells through the G4RP-RT-qPCR protocol. Overall, the results presented here represent a step towards the optimization of G4-RNAs identification, a key step in studying G4s in cell biology and human diseases.
机译:富含致鸟嘌呤的DNA和RNA序列可以折叠成称为G-Quadruplees(或G4-DNA和G4-RNA)的高阶结构。人类基因组,转录组和NCRNA组(非编码RNA)中G4景观的患病率,统称为G4 ome,强烈地暗示多水平的生物相关性(基因表达,复制)。小分子可用于追踪活细胞中的G4s,用于在细胞生物学的正常和疾病相关变化中的G4s功能表征。在这里,我们描述了作为Biotasq称为Biotasq的生物素化的生物米形配体及其作为分子工具的用途,其允许通过亲和下拉方案分离G4。我们通过通过G4RP-RT-QPCR方案从体外和人细胞从体外和人细胞纯化生物相关G4s来证明该方法的一般适用性。总的来说,这里提出的结果代表了促进了G4-RNAS鉴定的优化的步骤,这是研究细胞生物学和人类疾病中G4的关键步骤。

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