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Pseudoknot length modulates the folding, conformational dynamics, and robustness of Xrn1 resistance of flaviviral xrRNAs
To understand how RNA dynamics is regulated and connected to its function, we investigate the folding, conformational dynamics and robustness of Xrn1 resistance of a set of flaviviral xrRNAs using SAXS, smFRET and in vitro enzymatic assays. Flaviviral xrRNAs form discrete ring-like 3D structures, in...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8571300/ https://www.ncbi.nlm.nih.gov/pubmed/34741027 http://dx.doi.org/10.1038/s41467-021-26616-x |
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author | Niu, Xiaolin Sun, Ruirui Chen, Zhifeng Yao, Yirong Zuo, Xiaobing Chen, Chunlai Fang, Xianyang |
author_facet | Niu, Xiaolin Sun, Ruirui Chen, Zhifeng Yao, Yirong Zuo, Xiaobing Chen, Chunlai Fang, Xianyang |
author_sort | Niu, Xiaolin |
collection | PubMed |
description | To understand how RNA dynamics is regulated and connected to its function, we investigate the folding, conformational dynamics and robustness of Xrn1 resistance of a set of flaviviral xrRNAs using SAXS, smFRET and in vitro enzymatic assays. Flaviviral xrRNAs form discrete ring-like 3D structures, in which the length of a conserved long-range pseudoknot (PK2) ranges from 2 bp to 7 bp. We find that xrRNAs’ folding, conformational dynamics and Xrn1 resistance are strongly correlated and highly Mg(2+)-dependent, furthermore, the Mg(2+)-dependence is modulated by PK2 length variations. xrRNAs with long PK2 require less Mg(2+) to stabilize their folding, exhibit reduced conformational dynamics and strong Xrn1 resistance even at low Mg(2+), and tolerate mutations at key tertiary motifs at high Mg(2+), which generally are destructive to xrRNAs with short PK2. These results demonstrate an unusual regulatory mechanism of RNA dynamics providing insights into the functions and future biomedical applications of xrRNAs. |
format | Online Article Text |
id | pubmed-8571300 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-85713002021-11-15 Pseudoknot length modulates the folding, conformational dynamics, and robustness of Xrn1 resistance of flaviviral xrRNAs Niu, Xiaolin Sun, Ruirui Chen, Zhifeng Yao, Yirong Zuo, Xiaobing Chen, Chunlai Fang, Xianyang Nat Commun Article To understand how RNA dynamics is regulated and connected to its function, we investigate the folding, conformational dynamics and robustness of Xrn1 resistance of a set of flaviviral xrRNAs using SAXS, smFRET and in vitro enzymatic assays. Flaviviral xrRNAs form discrete ring-like 3D structures, in which the length of a conserved long-range pseudoknot (PK2) ranges from 2 bp to 7 bp. We find that xrRNAs’ folding, conformational dynamics and Xrn1 resistance are strongly correlated and highly Mg(2+)-dependent, furthermore, the Mg(2+)-dependence is modulated by PK2 length variations. xrRNAs with long PK2 require less Mg(2+) to stabilize their folding, exhibit reduced conformational dynamics and strong Xrn1 resistance even at low Mg(2+), and tolerate mutations at key tertiary motifs at high Mg(2+), which generally are destructive to xrRNAs with short PK2. These results demonstrate an unusual regulatory mechanism of RNA dynamics providing insights into the functions and future biomedical applications of xrRNAs. Nature Publishing Group UK 2021-11-05 /pmc/articles/PMC8571300/ /pubmed/34741027 http://dx.doi.org/10.1038/s41467-021-26616-x Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Niu, Xiaolin Sun, Ruirui Chen, Zhifeng Yao, Yirong Zuo, Xiaobing Chen, Chunlai Fang, Xianyang Pseudoknot length modulates the folding, conformational dynamics, and robustness of Xrn1 resistance of flaviviral xrRNAs |
title | Pseudoknot length modulates the folding, conformational dynamics, and robustness of Xrn1 resistance of flaviviral xrRNAs |
title_full | Pseudoknot length modulates the folding, conformational dynamics, and robustness of Xrn1 resistance of flaviviral xrRNAs |
title_fullStr | Pseudoknot length modulates the folding, conformational dynamics, and robustness of Xrn1 resistance of flaviviral xrRNAs |
title_full_unstemmed | Pseudoknot length modulates the folding, conformational dynamics, and robustness of Xrn1 resistance of flaviviral xrRNAs |
title_short | Pseudoknot length modulates the folding, conformational dynamics, and robustness of Xrn1 resistance of flaviviral xrRNAs |
title_sort | pseudoknot length modulates the folding, conformational dynamics, and robustness of xrn1 resistance of flaviviral xrrnas |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8571300/ https://www.ncbi.nlm.nih.gov/pubmed/34741027 http://dx.doi.org/10.1038/s41467-021-26616-x |
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