RNA triplexes: from structural principles to biological and biotech applications

被引:83
作者
Devi, Gitali [1 ]
Zhou, Yuan [1 ]
Zhong, Zhensheng [1 ]
Toh, Desiree-Faye Kaixin [1 ]
Chen, Gang [1 ]
机构
[1] Nanyang Technol Univ, Sch Phys & Math Sci, Div Chem & Biol Chem, Singapore 639798, Singapore
关键词
DOUBLE-STRANDED-RNA; PEPTIDE NUCLEIC-ACIDS; DOUBLE-HELICAL RNA; HIV-1 REV PROTEIN; GROUP-I INTRON; DOT-A PAIR; CRYSTAL-STRUCTURE; TERTIARY INTERACTIONS; CANDIDA-ALBICANS; NMR STRUCTURE;
D O I
10.1002/wrna.1261
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The diverse biological functions of RNA are determined by the complex structures of RNA stabilized by both secondary and tertiary interactions. An RNA triplex is an important tertiary structure motif that is found in many pseudoknots and other structured RNAs. A triplex structure usually forms through tertiary interactions in the major or minor groove of a Watson-Crick base-paired stem. A major-groove RNA triplex structure is stable in isolation by forming consecutive major-groove base triples such as U center dot A-U and C+center dot G-C. Minor-groove RNA triplexes, e.g., A-minor motif triplexes, are found in almost all large structured RNAs. As double-stranded RNA stem regions are often involved in biologically important tertiary triplex structure formation and protein binding, the ability to sequence specifically target any desired RNA duplexes by triplex formation would have great potential for biomedical applications. Programmable chemically modified triplex-forming oligonucleotides (TFOs) and triplex-forming peptide nucleic acids (PNAs) have been developed to form TFO center dot RNA(2) and PNA center dot RNA(2) triplexes, respectively, with enhanced binding affinity and sequence specificity at physiological conditions. Here, we (1) provide an overview of naturally occurring RNA triplexes, (2) summarize the experimental methods for studying triplexes, and (3) review the development of TFOs and triplex-forming PNAs for targeting an HIV-1 ribosomal frameshift-inducing RNA, a bacterial ribosomal A-site RNA, and a human microRNA hairpin precursor, and for inhibiting the RNA-protein interactions involving human RNA-dependent protein kinase and HIV-1 viral protein Rev. (C) 2014 JohnWiley & Sons, Ltd.
引用
收藏
页码:111 / 128
页数:18
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