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      Adenine Methylation Enhances the Conformational Flexibility of an RNA Hairpin Tetraloop

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      The Journal of Physical Chemistry. B
      American Chemical Society

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          Abstract

          The N 6-methyladenosine modification is one of the most abundant post-transcriptional modifications in ribonucleic acid (RNA) molecules. Using molecular dynamics simulations and alchemical free-energy calculations, we studied the structural and energetic implications of incorporating this modification in an adenine mononucleotide and an RNA hairpin structure. At the mononucleotide level, we found that the syn configuration is more favorable than the anti configuration by 2.05 ± 0.15 kcal/mol. The unfavorable effect of methylation was due to the steric overlap between the methyl group and a nitrogen atom in the purine ring. We then probed the effect of methylation in an RNA hairpin structure containing an AUCG tetraloop, which is recognized by a “reader” protein (YTHDC1) to promote transcriptional silencing of long noncoding RNAs. While methylation had no significant conformational effect on the hairpin stem, the methylated tetraloop showed enhanced conformational flexibility compared to the unmethylated tetraloop. The increased flexibility was associated with the outward flipping of two bases (A6 and U7) which formed stacking interactions with each other and with the C8 and G9 bases in the tetraloop, leading to a conformation similar to that in the RNA/reader protein complex. Therefore, methylation-induced conformational flexibility likely facilitates RNA recognition by the reader protein.

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              Comprehensive analysis of mRNA methylation reveals enrichment in 3' UTRs and near stop codons.

              Methylation of the N(6) position of adenosine (m(6)A) is a posttranscriptional modification of RNA with poorly understood prevalence and physiological relevance. The recent discovery that FTO, an obesity risk gene, encodes an m(6)A demethylase implicates m(6)A as an important regulator of physiological processes. Here, we present a method for transcriptome-wide m(6)A localization, which combines m(6)A-specific methylated RNA immunoprecipitation with next-generation sequencing (MeRIP-Seq). We use this method to identify mRNAs of 7,676 mammalian genes that contain m(6)A, indicating that m(6)A is a common base modification of mRNA. The m(6)A modification exhibits tissue-specific regulation and is markedly increased throughout brain development. We find that m(6)A sites are enriched near stop codons and in 3' UTRs, and we uncover an association between m(6)A residues and microRNA-binding sites within 3' UTRs. These findings provide a resource for identifying transcripts that are substrates for adenosine methylation and reveal insights into the epigenetic regulation of the mammalian transcriptome. Copyright © 2012 Elsevier Inc. All rights reserved.
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                Author and article information

                Journal
                J Phys Chem B
                J Phys Chem B
                jp
                jpcbfk
                The Journal of Physical Chemistry. B
                American Chemical Society
                1520-6106
                1520-5207
                27 March 2024
                04 April 2024
                : 128
                : 13
                : 3157-3166
                Affiliations
                Department of Chemical Engineering and Bioengineering, University of New Hampshire , Durham, New Hampshire 03824, United States
                Author notes
                Author information
                https://orcid.org/0000-0002-7950-9226
                https://orcid.org/0000-0002-2087-2880
                Article
                10.1021/acs.jpcb.4c00522
                11000223
                38535997
                fc5ce819-3d46-41ca-a6be-77ff70960ed2
                © 2024 The Authors. Published by American Chemical Society

                Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works ( https://creativecommons.org/licenses/by-nc-nd/4.0/).

                History
                : 25 January 2024
                : 14 March 2024
                : 10 March 2024
                Funding
                Funded by: National Science Foundation, doi 10.13039/100000001;
                Award ID: OIA-1757371
                Funded by: National Institute of General Medical Sciences, doi 10.13039/100000057;
                Award ID: R35GM138217
                Categories
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                Custom metadata
                jp4c00522
                jp4c00522

                Physical chemistry
                Physical chemistry

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