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Structural basis for water modulating RNA duplex formation in the CUG repeats of myotonic dystrophy type 1
Secondary structures formed by expanded CUG RNA are involved in the pathobiology of myotonic dystrophy type 1. Understanding the molecular basis of toxic RNA structures can provide insights into the mechanism of disease pathogenesis and accelerate the drug discovery process. Here, we report the crys...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Biochemistry and Molecular Biology
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10316006/ https://www.ncbi.nlm.nih.gov/pubmed/37245780 http://dx.doi.org/10.1016/j.jbc.2023.104864 |
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author | Wang, Shun-Ching Chen, Yi-Tsao Satange, Roshan Chu, Jhih-Wei Hou, Ming-Hon |
author_facet | Wang, Shun-Ching Chen, Yi-Tsao Satange, Roshan Chu, Jhih-Wei Hou, Ming-Hon |
author_sort | Wang, Shun-Ching |
collection | PubMed |
description | Secondary structures formed by expanded CUG RNA are involved in the pathobiology of myotonic dystrophy type 1. Understanding the molecular basis of toxic RNA structures can provide insights into the mechanism of disease pathogenesis and accelerate the drug discovery process. Here, we report the crystal structure of CUG repeat RNA containing three U–U mismatches between C–G and G–C base pairs. The CUG RNA crystallizes as an A-form duplex, with the first and third U–U mismatches adopting a water-mediated asymmetric mirror isoform geometry. We found for the first time that a symmetric, water-bridged U-H(2)O-U mismatch is well tolerated within the CUG RNA duplex, which was previously suspected but not observed. The new water-bridged U–U mismatch resulted in high base-pair opening and single-sided cross-strand stacking interactions, which in turn dominate the CUG RNA structure. Furthermore, we performed molecular dynamics simulations that complemented the structural findings and proposed that the first and third U–U mismatches are interchangeable conformations, while the central water-bridged U–U mismatch represents an intermediate state that modulates the RNA duplex conformation. Collectively, the new structural features provided in this work are important for understanding the recognition of U–U mismatches in CUG repeats by external ligands such as proteins or small molecules. |
format | Online Article Text |
id | pubmed-10316006 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Society for Biochemistry and Molecular Biology |
record_format | MEDLINE/PubMed |
spelling | pubmed-103160062023-07-04 Structural basis for water modulating RNA duplex formation in the CUG repeats of myotonic dystrophy type 1 Wang, Shun-Ching Chen, Yi-Tsao Satange, Roshan Chu, Jhih-Wei Hou, Ming-Hon J Biol Chem Research Article Secondary structures formed by expanded CUG RNA are involved in the pathobiology of myotonic dystrophy type 1. Understanding the molecular basis of toxic RNA structures can provide insights into the mechanism of disease pathogenesis and accelerate the drug discovery process. Here, we report the crystal structure of CUG repeat RNA containing three U–U mismatches between C–G and G–C base pairs. The CUG RNA crystallizes as an A-form duplex, with the first and third U–U mismatches adopting a water-mediated asymmetric mirror isoform geometry. We found for the first time that a symmetric, water-bridged U-H(2)O-U mismatch is well tolerated within the CUG RNA duplex, which was previously suspected but not observed. The new water-bridged U–U mismatch resulted in high base-pair opening and single-sided cross-strand stacking interactions, which in turn dominate the CUG RNA structure. Furthermore, we performed molecular dynamics simulations that complemented the structural findings and proposed that the first and third U–U mismatches are interchangeable conformations, while the central water-bridged U–U mismatch represents an intermediate state that modulates the RNA duplex conformation. Collectively, the new structural features provided in this work are important for understanding the recognition of U–U mismatches in CUG repeats by external ligands such as proteins or small molecules. American Society for Biochemistry and Molecular Biology 2023-05-26 /pmc/articles/PMC10316006/ /pubmed/37245780 http://dx.doi.org/10.1016/j.jbc.2023.104864 Text en © 2023 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Research Article Wang, Shun-Ching Chen, Yi-Tsao Satange, Roshan Chu, Jhih-Wei Hou, Ming-Hon Structural basis for water modulating RNA duplex formation in the CUG repeats of myotonic dystrophy type 1 |
title | Structural basis for water modulating RNA duplex formation in the CUG repeats of myotonic dystrophy type 1 |
title_full | Structural basis for water modulating RNA duplex formation in the CUG repeats of myotonic dystrophy type 1 |
title_fullStr | Structural basis for water modulating RNA duplex formation in the CUG repeats of myotonic dystrophy type 1 |
title_full_unstemmed | Structural basis for water modulating RNA duplex formation in the CUG repeats of myotonic dystrophy type 1 |
title_short | Structural basis for water modulating RNA duplex formation in the CUG repeats of myotonic dystrophy type 1 |
title_sort | structural basis for water modulating rna duplex formation in the cug repeats of myotonic dystrophy type 1 |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10316006/ https://www.ncbi.nlm.nih.gov/pubmed/37245780 http://dx.doi.org/10.1016/j.jbc.2023.104864 |
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