The theory of helix-based RNA folding kinetics and its application*

被引:2
作者
Gong, Sha [1 ]
Liu, Taigang [2 ]
Wang, Yanli [2 ]
Zhang, Wenbing [2 ]
机构
[1] Huanggang Normal Univ, Hubei Collaborat Innovat Ctr Characterist Resourc, Hubei Key Lab Econ Forest Germplasm Improvement &, Huanggang 438000, Peoples R China
[2] Wuhan Univ, Dept Phys, Wuhan 430072, Peoples R China
基金
中国国家自然科学基金;
关键词
RNA folding kinetics; RNA structure; Riboswitch; HDV ribozyme; CONTROLS GENE-EXPRESSION; CONFORMATIONAL DYNAMICS; SECONDARY STRUCTURE; TERTIARY STRUCTURE; RIBOSWITCH; TRANSCRIPTION; MECHANISM; RIBOZYME; LIGAND; MG2+;
D O I
10.1088/1674-1056/abab84
中图分类号
O4 [物理学];
学科分类号
0702 ;
摘要
RNAs carry out diverse biological functions, partly because different conformations of the same RNA sequence can play different roles in cellular activities. To fully understand the biological functions of RNAs requires a conceptual framework to investigate the folding kinetics of RNA molecules, instead of native structures alone. Over the past several decades, many experimental and theoretical methods have been developed to address RNA folding. The helix-based RNA folding theory is the one which uses helices as building blocks, to calculate folding kinetics of secondary structures with pseudoknots of long RNA in two different folding scenarios. Here, we will briefly review the helix-based RNA folding theory and its application in exploring regulation mechanisms of several riboswitches and self-cleavage activities of the hepatitis delta virus (HDV) ribozyme.
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页数:8
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