RNA Duplex Map in Living Cells Reveals Higher-Order Transcriptome Structure
Author(s) -
Zhipeng Lu,
Qiangfeng Cliff Zhang,
Byron Lee,
Ryan A. Flynn,
Martin A. Smith,
James Robinson,
Chen Davidovich,
Anne R. Gooding,
Karen J. Goodrich,
John S. Mattick,
Jill P. Mesirov,
Thomas R. Cech,
Howard Y. Chang
Publication year - 2016
Publication title -
cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 26.304
H-Index - 776
eISSN - 1097-4172
pISSN - 0092-8674
DOI - 10.1016/j.cell.2016.04.028
Subject(s) - biology , xist , rna , non coding rna , genetics , computational biology , rna silencing , base pair , ribonucleoprotein , transcriptome , nucleic acid structure , interactome , gene , gene expression , x chromosome , rna interference , x inactivation
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. VIDEO ABSTRACT.
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