Computational Methods to Study DNA:DNA:RNA Triplex Formation by lncRNAs.

Noncoding RNA

Institute for Cardiovascular Physiology, Goethe University, 60590 Frankfurt, Germany.

Published: January 2023

Long non-coding RNAs (lncRNAs) impact cell function via numerous mechanisms. In the nucleus, interactions between lncRNAs and DNA and the consequent formation of non-canonical nucleic acid structures seems to be particularly relevant. Along with interactions between single-stranded RNA (ssRNA) and single-stranded DNA (ssDNA), such as R-loops, ssRNA can also interact with double-stranded DNA (dsDNA) to form DNA:DNA:RNA triplexes. A major challenge in the study of DNA:DNA:RNA triplexes is the identification of the precise RNA component interacting with specific regions of the dsDNA. As this is a crucial step towards understanding lncRNA function, there exist several computational methods designed to predict these sequences. This review summarises the recent progress in the prediction of triplex formation and highlights important DNA:DNA:RNA triplexes. In particular, different prediction tools (, , , , , and ) will be discussed and their use exemplified by selected lncRNAs, whose DNA:DNA:RNA triplex forming potential was validated experimentally. Collectively, these tools revealed that DNA:DNA:RNA triplexes are likely to be numerous and make important contributions to gene expression regulation.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9965544PMC
http://dx.doi.org/10.3390/ncrna9010010DOI Listing

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Article Synopsis
  • Long noncoding RNAs (lncRNAs) play a significant role in regulating DNA, RNA, and protein interactions but direct binding to DNA is not commonly shown.
  • This text outlines computational strategies for identifying lncRNAs that can bind to chromatin through stable DNA-DNA-RNA triplex formations.
  • Additionally, it highlights biophysical methods for experimentally validating the lncRNA-target gene interactions selected through computational means.
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