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Three-dimensional genome organization via triplex-forming RNAs.

Irene FarabellaMarco Di StefanoPaula Soler-VilaMaria Marti-MarimonMarc A Marti-Renom
Published in: Nature structural & molecular biology (2021)
An increasing number of long noncoding RNAs (lncRNAs) have been proposed to act as nuclear organization factors during interphase. Direct RNA-DNA interactions can be achieved by the formation of triplex helix structures where a single-stranded RNA molecule hybridizes by complementarity into the major groove of double-stranded DNA. However, whether and how these direct RNA-DNA associations influence genome structure in interphase chromosomes remain poorly understood. Here we theorize that RNA organizes the genome in space via a triplex-forming mechanism. To test this theory, we apply a computational modeling approach of chromosomes that combines restraint-based modeling with polymer physics. Our models suggest that colocalization of triplex hotspots targeted by lncRNAs could contribute to large-scale chromosome compartmentalization cooperating, rather than competing, with architectural transcription factors such as CTCF.
Keyphrases
  • nucleic acid
  • circulating tumor
  • cell free
  • single molecule
  • transcription factor
  • genome wide
  • binding protein
  • high resolution
  • dna binding
  • genome wide identification
  • mass spectrometry
  • copy number