Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/98149
Title: Recognition of RNA duplexes by chemically modified triplex-forming oligonucleotides
Authors: Zhou, Y.
Kierzek, E.
Loo, Z. P.
Antonio, M.
Yau, Yin Hoe
Chuah, Y. W.
Geifman-Shochat, Susana
Kierzek, R.
Chen, Gang
Issue Date: 2013
Source: Zhou, Y., Kierzek, E., Loo, Z. P., Antonio, M., Yau, Y. H., Chuah, Y. W., Geifman-Shochat, S., Kierzek, R.,& Chen, G. (2013). Recognition of RNA duplexes by chemically modified triplex-forming oligonucleotides. Nucleic Acids Research, 41(13), 6664-6673.
Series/Report no.: Nucleic acids research
Abstract: Triplex is emerging as an important RNA tertiary structure motif, in which consecutive non-canonical base pairs form between a duplex and a third strand. RNA duplex region is also often functionally important site for protein binding. Thus, triplex-forming oligonucleotides (TFOs) may be developed to regulate various biological functions involving RNA, such as viral ribosomal frameshifting and reverse transcription. How chemical modification in TFOs affects RNA triplex stability, however, is not well understood. Here, we incorporated locked nucleic acid, 2-thio U- and 2′-O methyl-modified residues in a series of all pyrimidine RNA TFOs, and we studied the binding to two RNA hairpin structures. The 12-base-triple major-groove pyrimidine–purine–pyrimidine triplex structures form between the duplex regions of RNA/DNA hairpins and the complementary RNA TFOs. Ultraviolet-absorbance-detected thermal melting studies reveal that the locked nucleic acid and 2-thio U modifications in TFOs strongly enhance triplex formation with both parental RNA and DNA duplex regions. In addition, we found that incorporation of 2′-O methyl-modified residues in a TFO destabilizes and stabilizes triplex formation with RNA and DNA duplex regions, respectively. The (de)stabilization of RNA triplex formation may be facilitated through modulation of van der Waals contact, base stacking, hydrogen bonding, backbone pre-organization, geometric compatibility and/or dehydration energy. Better understanding of the molecular determinants of RNA triplex structure stability lays the foundation for designing and discovering novel sequence-specific duplex-binding ligands as diagnostic and therapeutic agents targeting RNA.
URI: https://hdl.handle.net/10356/98149
http://hdl.handle.net/10220/13310
DOI: http://dx.doi.org/10.1093/nar/gkt352
Rights: © 2013 The Author(s). Published by Oxford University Press. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
Fulltext Permission: open
Fulltext Availability: With Fulltext
Appears in Collections:SBS Journal Articles
SPMS Journal Articles

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