Unravelling the roles of non-Watson-Crick and triplex structures in regulating RNA folding dynamics and function

It is not well understood how the RNA folding and unfolding dynamics, mechanical properties, and biological functions are affected by non-Watson-Crick pairs and base triples. Using a human telomerase RNA hairpin containing four consecutive non-canonical base pairs as a model system, we studied the e...

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Main Author: Zhong, Zhensheng
Other Authors: Chen Gang
Format: Theses and Dissertations
Language:English
Published: 2016
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Online Access:https://hdl.handle.net/10356/66532
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Institution: Nanyang Technological University
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spelling sg-ntu-dr.10356-665322023-02-28T23:47:14Z Unravelling the roles of non-Watson-Crick and triplex structures in regulating RNA folding dynamics and function Zhong, Zhensheng Chen Gang School of Physical and Mathematical Sciences DRNTU::Science::Biological sciences::Genetics It is not well understood how the RNA folding and unfolding dynamics, mechanical properties, and biological functions are affected by non-Watson-Crick pairs and base triples. Using a human telomerase RNA hairpin containing four consecutive non-canonical base pairs as a model system, we studied the effect of U∙U pair to U∙C pair substitutions on thermodynamic and mechanical properties. The ensemble thermal denaturation of the hairpins shows a 3-state pathway with an on-pathway intermediate with the disruption of the non-canonical base paired region as well as two apical Watson-Crick base pairs. In single molecule force spectroscopic studies, a misfolded hairpin at forces below 13 pN is observed. The single U·U to U·C substitution lowers the melting temperature of the first transition in thermal denaturation and significantly lowers the mechanical unfolding rupture force without obviously affecting the unfolding transition-state position. Furthermore, the substitution increases the frequency of misfolding and the mechanical folding rates, and shifts the folding transition-state position towards the native hairpin structure. Our results clearly demonstrate the non-nearest-neighbor effects of the U·U to U·C substitution. Many RNA viruses including Simian Retrovirus type 1 (SRV-1) utilize minus-one ribosomal frameshifting as an alternative translation mechanism to generate stable ratios of structural and catalytic proteins. The detailed mechanism of minus-one ribosomal frameshifting is still not well understood. The SRV-1 frameshifting pseudoknot is located in the overlapping region of gag and pol genes and plays critical roles in stimulating frameshifting. Using optical tweezers, we studied the mechanical properties of a series of pseudoknots derived from the wildtype SRV-1 frameshifting pseudoknot. In addition, we carried out ensemble thermal denaturation and native polyacrylamide gel electrophoresis studies. Our studies reveal that the minor-groove base triple formation in the pseudoknot enhances the structural compactness and mechanical stability. The −1 frameshifting efficiency is positively correlated with one-step unfolding rupture force and inversely correlated with the unfolding rate. CHEMISTRY and BIOLOGICAL CHEMISTRY 2016-04-15T03:48:10Z 2016-04-15T03:48:10Z 2016 Thesis Zhong, Z. (2016). Unravelling the roles of non-Watson-Crick and triplex structures in regulating RNA folding dynamics and function. Doctoral thesis, Nanyang Technological University, Singapore. https://hdl.handle.net/10356/66532 10.32657/10356/66532 en 88 p. application/pdf
institution Nanyang Technological University
building NTU Library
continent Asia
country Singapore
Singapore
content_provider NTU Library
collection DR-NTU
language English
topic DRNTU::Science::Biological sciences::Genetics
spellingShingle DRNTU::Science::Biological sciences::Genetics
Zhong, Zhensheng
Unravelling the roles of non-Watson-Crick and triplex structures in regulating RNA folding dynamics and function
description It is not well understood how the RNA folding and unfolding dynamics, mechanical properties, and biological functions are affected by non-Watson-Crick pairs and base triples. Using a human telomerase RNA hairpin containing four consecutive non-canonical base pairs as a model system, we studied the effect of U∙U pair to U∙C pair substitutions on thermodynamic and mechanical properties. The ensemble thermal denaturation of the hairpins shows a 3-state pathway with an on-pathway intermediate with the disruption of the non-canonical base paired region as well as two apical Watson-Crick base pairs. In single molecule force spectroscopic studies, a misfolded hairpin at forces below 13 pN is observed. The single U·U to U·C substitution lowers the melting temperature of the first transition in thermal denaturation and significantly lowers the mechanical unfolding rupture force without obviously affecting the unfolding transition-state position. Furthermore, the substitution increases the frequency of misfolding and the mechanical folding rates, and shifts the folding transition-state position towards the native hairpin structure. Our results clearly demonstrate the non-nearest-neighbor effects of the U·U to U·C substitution. Many RNA viruses including Simian Retrovirus type 1 (SRV-1) utilize minus-one ribosomal frameshifting as an alternative translation mechanism to generate stable ratios of structural and catalytic proteins. The detailed mechanism of minus-one ribosomal frameshifting is still not well understood. The SRV-1 frameshifting pseudoknot is located in the overlapping region of gag and pol genes and plays critical roles in stimulating frameshifting. Using optical tweezers, we studied the mechanical properties of a series of pseudoknots derived from the wildtype SRV-1 frameshifting pseudoknot. In addition, we carried out ensemble thermal denaturation and native polyacrylamide gel electrophoresis studies. Our studies reveal that the minor-groove base triple formation in the pseudoknot enhances the structural compactness and mechanical stability. The −1 frameshifting efficiency is positively correlated with one-step unfolding rupture force and inversely correlated with the unfolding rate.
author2 Chen Gang
author_facet Chen Gang
Zhong, Zhensheng
format Theses and Dissertations
author Zhong, Zhensheng
author_sort Zhong, Zhensheng
title Unravelling the roles of non-Watson-Crick and triplex structures in regulating RNA folding dynamics and function
title_short Unravelling the roles of non-Watson-Crick and triplex structures in regulating RNA folding dynamics and function
title_full Unravelling the roles of non-Watson-Crick and triplex structures in regulating RNA folding dynamics and function
title_fullStr Unravelling the roles of non-Watson-Crick and triplex structures in regulating RNA folding dynamics and function
title_full_unstemmed Unravelling the roles of non-Watson-Crick and triplex structures in regulating RNA folding dynamics and function
title_sort unravelling the roles of non-watson-crick and triplex structures in regulating rna folding dynamics and function
publishDate 2016
url https://hdl.handle.net/10356/66532
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