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In vivo probing of nascent RNA structures reveals principles of cotranscriptional folding
Author(s) -
Danny Incarnato,
Edoardo Morandi,
Francesca Anselmi,
Lisa Marie Simon,
Giulia Basile,
Salvatore Oliviero
Publication year - 2017
Publication title -
nucleic acids research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 9.008
H-Index - 537
eISSN - 1362-4954
pISSN - 0305-1048
DOI - 10.1093/nar/gkx617
Subject(s) - biology , rna , computational biology , transcriptome , folding (dsp implementation) , transcription (linguistics) , base pair , nucleic acid structure , genetics , protein folding , microbiology and biotechnology , gene , gene expression , linguistics , philosophy , electrical engineering , engineering
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.

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