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RNA Duplex Map in Living Cells Reveals Higher-Order Transcriptome Structure

机译:活细胞中的RNA双链体图揭示了更高阶的转录组结构。

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RNA has the intrinsic property to base pair, forming complex structures fundamental to its diverse functions. Here, we develop PARIS, a method based on reversible psoralen crosslinking for global mapping of RNA duplexes with near base-pair resolution in living cells. PARIS analysis in three human and mouse cell types reveals frequent long-range structures, higher-order architectures, and RNA-RNA interactions in trans across the transcriptome. PARIS determines base-pairing interactions on an individual-molecule level, revealing pervasive alternative conformations. We used PARIS-determined helices to guide phylogenetic analysis of RNA structures and discovered conserved long-range and alternative structures. XIST, a long noncoding RNA (lncRNA) essential for X chromosome inactivation, folds into evolutionarily conserved RNA structural domains that span many kilobases. XIST A-repeat forms complex inter-repeat duplexes that nucleate higher-order assembly of the key epigenetic silencing protein SPEN. PARIS is a generally applicable and versatile method that provides novel insights into the RNA structurome and interactome.
机译:RNA具有碱基对的固有特性,形成了对其多种功能至关重要的复杂结构。在这里,我们开发PARIS,一种基于可逆补骨脂素交联的方法,用于在活细胞中以接近碱基对的分辨率对RNA双链体进行全局定位。在三种人类和小鼠细胞类型中的PARIS分析揭示了跨转录组的频繁的长距离结构,高阶结构以及RNA-RNA相互作用。 PARIS在单个分子水平上确定碱基配对相互作用,揭示了普遍的替代构象。我们使用PARIS确定的螺旋来指导RNA结构的系统发育分析,并发现了保守的远程和替代结构。 XIST是X染色体失活所必需的长的非编码RNA(lncRNA),可折叠成跨越多个千碱基的进化保守的RNA结构域。 XIST A重复序列形成复杂的重复序列间双链体,使关键的表观遗传沉默蛋白SPEN的高阶装配成核。 PARIS是一种普遍适用的通用方法,可提供有关RNA结构体和相互作用组的新颖见解。

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