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Virtual High-Throughput Screening Identifies Mycophenolic Acid as a Novel RNA Capping Inhibitor

The RNA guanylyltransferase (GTase) is involved in the synthesis of the (m7)Gppp-RNA cap structure found at the 5′ end of eukaryotic mRNAs. GTases are members of the covalent nucleotidyl transferase superfamily, which also includes DNA and RNA ligases. GTases catalyze a two-step reaction in which th...

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Autores principales: Tremblay-Létourneau, Maude, Despins, Simon, Bougie, Isabelle, Bisaillon, Martin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3174198/
https://www.ncbi.nlm.nih.gov/pubmed/21935470
http://dx.doi.org/10.1371/journal.pone.0024806
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author Tremblay-Létourneau, Maude
Despins, Simon
Bougie, Isabelle
Bisaillon, Martin
author_facet Tremblay-Létourneau, Maude
Despins, Simon
Bougie, Isabelle
Bisaillon, Martin
author_sort Tremblay-Létourneau, Maude
collection PubMed
description The RNA guanylyltransferase (GTase) is involved in the synthesis of the (m7)Gppp-RNA cap structure found at the 5′ end of eukaryotic mRNAs. GTases are members of the covalent nucleotidyl transferase superfamily, which also includes DNA and RNA ligases. GTases catalyze a two-step reaction in which they initially utilize GTP as a substrate to form a covalent enzyme-GMP intermediate. The GMP moiety is then transferred to the diphosphate end of the RNA transcript in the second step of the reaction to form the Gppp-RNA structure. In the current study, we used a combination of virtual database screening, homology modeling, and biochemical assays to search for novel GTase inhibitors. Using this approach, we demonstrate that mycophenolic acid (MPA) can inhibit the GTase reaction by preventing the catalytic transfer of the GMP moiety onto an acceptor RNA. As such, MPA represents a novel type of inhibitor against RNA guanylyltransferases that inhibits the second step of the catalytic reaction. Moreover, we show that the addition of MPA to S. cerevisiae cells leads to a reduction of capped mRNAs. Finally, biochemical assays also demonstrate that MPA can inhibit DNA ligases through inhibition of the second step of the reaction. The biological implications of these findings for the MPA-mediated inhibition of members of the covalent nucleotidyl superfamily are discussed.
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spelling pubmed-31741982011-09-20 Virtual High-Throughput Screening Identifies Mycophenolic Acid as a Novel RNA Capping Inhibitor Tremblay-Létourneau, Maude Despins, Simon Bougie, Isabelle Bisaillon, Martin PLoS One Research Article The RNA guanylyltransferase (GTase) is involved in the synthesis of the (m7)Gppp-RNA cap structure found at the 5′ end of eukaryotic mRNAs. GTases are members of the covalent nucleotidyl transferase superfamily, which also includes DNA and RNA ligases. GTases catalyze a two-step reaction in which they initially utilize GTP as a substrate to form a covalent enzyme-GMP intermediate. The GMP moiety is then transferred to the diphosphate end of the RNA transcript in the second step of the reaction to form the Gppp-RNA structure. In the current study, we used a combination of virtual database screening, homology modeling, and biochemical assays to search for novel GTase inhibitors. Using this approach, we demonstrate that mycophenolic acid (MPA) can inhibit the GTase reaction by preventing the catalytic transfer of the GMP moiety onto an acceptor RNA. As such, MPA represents a novel type of inhibitor against RNA guanylyltransferases that inhibits the second step of the catalytic reaction. Moreover, we show that the addition of MPA to S. cerevisiae cells leads to a reduction of capped mRNAs. Finally, biochemical assays also demonstrate that MPA can inhibit DNA ligases through inhibition of the second step of the reaction. The biological implications of these findings for the MPA-mediated inhibition of members of the covalent nucleotidyl superfamily are discussed. Public Library of Science 2011-09-15 /pmc/articles/PMC3174198/ /pubmed/21935470 http://dx.doi.org/10.1371/journal.pone.0024806 Text en Tremblay-Létourneau et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Tremblay-Létourneau, Maude
Despins, Simon
Bougie, Isabelle
Bisaillon, Martin
Virtual High-Throughput Screening Identifies Mycophenolic Acid as a Novel RNA Capping Inhibitor
title Virtual High-Throughput Screening Identifies Mycophenolic Acid as a Novel RNA Capping Inhibitor
title_full Virtual High-Throughput Screening Identifies Mycophenolic Acid as a Novel RNA Capping Inhibitor
title_fullStr Virtual High-Throughput Screening Identifies Mycophenolic Acid as a Novel RNA Capping Inhibitor
title_full_unstemmed Virtual High-Throughput Screening Identifies Mycophenolic Acid as a Novel RNA Capping Inhibitor
title_short Virtual High-Throughput Screening Identifies Mycophenolic Acid as a Novel RNA Capping Inhibitor
title_sort virtual high-throughput screening identifies mycophenolic acid as a novel rna capping inhibitor
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3174198/
https://www.ncbi.nlm.nih.gov/pubmed/21935470
http://dx.doi.org/10.1371/journal.pone.0024806
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