Incarnato Danny, Morandi Edoardo, Anselmi Francesca, Simon Lisa M, Basile Giulia, Oliviero Salvatore
Dipartimento di Scienze della Vita e Biologia dei Sistemi, Università di Torino, Via Accademia Albertina, 13, Torino, Italy.
Italian Institute for Genomic Medicine (IIGM), Via Nizza 52, 10126 Torino, Italy.
Nucleic Acids Res. 2017 Sep 19;45(16):9716-9725. doi: 10.1093/nar/gkx617.
Defining the in vivo folding pathway of cellular RNAs is essential to understand how they reach their final native conformation. We here introduce a novel method, named Structural Probing of Elongating Transcripts (SPET-seq), that permits single-base resolution analysis of transcription intermediates' secondary structures on a transcriptome-wide scale, enabling base-resolution analysis of the RNA folding events. Our results suggest that cotranscriptional RNA folding in vivo is a mixture of cooperative folding events, in which local RNA secondary structure elements are formed as they get transcribed, and non-cooperative events, in which 5'-halves of long-range helices get sequestered into transient non-native interactions until their 3' counterparts have been transcribed. Together our work provides the first transcriptome-scale overview of RNA cotranscriptional folding in a living organism.
定义细胞RNA在体内的折叠途径对于理解它们如何达到最终天然构象至关重要。我们在此介绍一种名为延伸转录本结构探测(SPET-seq)的新方法,该方法允许在全转录组范围内对转录中间体的二级结构进行单碱基分辨率分析,从而实现对RNA折叠事件的碱基分辨率分析。我们的结果表明,体内共转录RNA折叠是协同折叠事件和非协同事件的混合,其中局部RNA二级结构元件在转录时形成,而非协同事件中,长程螺旋的5'端被隔离到瞬时非天然相互作用中,直到其3'对应部分被转录。我们的工作共同提供了活生物体中RNA共转录折叠的首个转录组规模概述。