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A potentially abundant junctional RNA motif stabilized by m(6)A and Mg(2+)
N(6)-Methyladenosine (m(6)A) is an abundant post-transcriptional RNA modification that influences multiple aspects of gene expression. In addition to recruiting proteins, m(6)A can modulate RNA function by destabilizing base pairing. Here, we show that when neighbored by a 5ʹ bulge, m(6)A stabilizes...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6050335/ https://www.ncbi.nlm.nih.gov/pubmed/30018356 http://dx.doi.org/10.1038/s41467-018-05243-z |
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author | Liu, Bei Merriman, Dawn K. Choi, Seung H. Schumacher, Maria A. Plangger, Raphael Kreutz, Christoph Horner, Stacy M. Meyer, Kate D. Al-Hashimi, Hashim M. |
author_facet | Liu, Bei Merriman, Dawn K. Choi, Seung H. Schumacher, Maria A. Plangger, Raphael Kreutz, Christoph Horner, Stacy M. Meyer, Kate D. Al-Hashimi, Hashim M. |
author_sort | Liu, Bei |
collection | PubMed |
description | N(6)-Methyladenosine (m(6)A) is an abundant post-transcriptional RNA modification that influences multiple aspects of gene expression. In addition to recruiting proteins, m(6)A can modulate RNA function by destabilizing base pairing. Here, we show that when neighbored by a 5ʹ bulge, m(6)A stabilizes m(6)A–U base pairs, and global RNA structure by ~1 kcal mol(−1). The bulge most likely provides the flexibility needed to allow optimal stacking between the methyl group and 3ʹ neighbor through a conformation that is stabilized by Mg(2+). A bias toward this motif can help explain the global impact of methylation on RNA structure in transcriptome-wide studies. While m(6)A embedded in duplex RNA is poorly recognized by the YTH domain reader protein and m(6)A antibodies, both readily recognize m(6)A in this newly identified motif. The results uncover potentially abundant and functional m(6)A motifs that can modulate the epitranscriptomic structure landscape with important implications for the interpretation of transcriptome-wide data. |
format | Online Article Text |
id | pubmed-6050335 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-60503352018-07-23 A potentially abundant junctional RNA motif stabilized by m(6)A and Mg(2+) Liu, Bei Merriman, Dawn K. Choi, Seung H. Schumacher, Maria A. Plangger, Raphael Kreutz, Christoph Horner, Stacy M. Meyer, Kate D. Al-Hashimi, Hashim M. Nat Commun Article N(6)-Methyladenosine (m(6)A) is an abundant post-transcriptional RNA modification that influences multiple aspects of gene expression. In addition to recruiting proteins, m(6)A can modulate RNA function by destabilizing base pairing. Here, we show that when neighbored by a 5ʹ bulge, m(6)A stabilizes m(6)A–U base pairs, and global RNA structure by ~1 kcal mol(−1). The bulge most likely provides the flexibility needed to allow optimal stacking between the methyl group and 3ʹ neighbor through a conformation that is stabilized by Mg(2+). A bias toward this motif can help explain the global impact of methylation on RNA structure in transcriptome-wide studies. While m(6)A embedded in duplex RNA is poorly recognized by the YTH domain reader protein and m(6)A antibodies, both readily recognize m(6)A in this newly identified motif. The results uncover potentially abundant and functional m(6)A motifs that can modulate the epitranscriptomic structure landscape with important implications for the interpretation of transcriptome-wide data. Nature Publishing Group UK 2018-07-17 /pmc/articles/PMC6050335/ /pubmed/30018356 http://dx.doi.org/10.1038/s41467-018-05243-z Text en © The Author(s) 2018 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/. |
spellingShingle | Article Liu, Bei Merriman, Dawn K. Choi, Seung H. Schumacher, Maria A. Plangger, Raphael Kreutz, Christoph Horner, Stacy M. Meyer, Kate D. Al-Hashimi, Hashim M. A potentially abundant junctional RNA motif stabilized by m(6)A and Mg(2+) |
title | A potentially abundant junctional RNA motif stabilized by m(6)A and Mg(2+) |
title_full | A potentially abundant junctional RNA motif stabilized by m(6)A and Mg(2+) |
title_fullStr | A potentially abundant junctional RNA motif stabilized by m(6)A and Mg(2+) |
title_full_unstemmed | A potentially abundant junctional RNA motif stabilized by m(6)A and Mg(2+) |
title_short | A potentially abundant junctional RNA motif stabilized by m(6)A and Mg(2+) |
title_sort | potentially abundant junctional rna motif stabilized by m(6)a and mg(2+) |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6050335/ https://www.ncbi.nlm.nih.gov/pubmed/30018356 http://dx.doi.org/10.1038/s41467-018-05243-z |
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