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Pre‐mRNA splicing is modulated by antifungal drugs in the filamentous fungus Neurospora crassa

For this study, we sought to identify pre‐mRNA processing events modulated by changes in extracellular pH, inorganic phosphate, and antifungal drugs. We examined genes with at least four putative introns whose transcriptional level responded to these effectors. We showed that the intron retention le...

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Autores principales: Mendes, Niege S., Silva, Patricia M., Silva‐Rocha, Rafael, Martinez‐Rossi, Nilce M., Rossi, Antonio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4821360/
https://www.ncbi.nlm.nih.gov/pubmed/27239448
http://dx.doi.org/10.1002/2211-5463.12047
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author Mendes, Niege S.
Silva, Patricia M.
Silva‐Rocha, Rafael
Martinez‐Rossi, Nilce M.
Rossi, Antonio
author_facet Mendes, Niege S.
Silva, Patricia M.
Silva‐Rocha, Rafael
Martinez‐Rossi, Nilce M.
Rossi, Antonio
author_sort Mendes, Niege S.
collection PubMed
description For this study, we sought to identify pre‐mRNA processing events modulated by changes in extracellular pH, inorganic phosphate, and antifungal drugs. We examined genes with at least four putative introns whose transcriptional level responded to these effectors. We showed that the intron retention levels of genes encoding asparagine synthetase 2, C6‐zinc finger regulator (fluffy), and a farnesyltransferase respond to amphotericin B, ketoconazole, and other effectors. In general, the assayed antifungals promoted the disruption of the structural domains of these proteins probably leading to their inactivation, which emphasize the complexity of the metabolic modulation exerted by antifungal signaling.
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spelling pubmed-48213602016-05-27 Pre‐mRNA splicing is modulated by antifungal drugs in the filamentous fungus Neurospora crassa Mendes, Niege S. Silva, Patricia M. Silva‐Rocha, Rafael Martinez‐Rossi, Nilce M. Rossi, Antonio FEBS Open Bio Research Articles For this study, we sought to identify pre‐mRNA processing events modulated by changes in extracellular pH, inorganic phosphate, and antifungal drugs. We examined genes with at least four putative introns whose transcriptional level responded to these effectors. We showed that the intron retention levels of genes encoding asparagine synthetase 2, C6‐zinc finger regulator (fluffy), and a farnesyltransferase respond to amphotericin B, ketoconazole, and other effectors. In general, the assayed antifungals promoted the disruption of the structural domains of these proteins probably leading to their inactivation, which emphasize the complexity of the metabolic modulation exerted by antifungal signaling. John Wiley and Sons Inc. 2016-03-14 /pmc/articles/PMC4821360/ /pubmed/27239448 http://dx.doi.org/10.1002/2211-5463.12047 Text en © 2016 The Authors. Published by FEBS Press and John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Mendes, Niege S.
Silva, Patricia M.
Silva‐Rocha, Rafael
Martinez‐Rossi, Nilce M.
Rossi, Antonio
Pre‐mRNA splicing is modulated by antifungal drugs in the filamentous fungus Neurospora crassa
title Pre‐mRNA splicing is modulated by antifungal drugs in the filamentous fungus Neurospora crassa
title_full Pre‐mRNA splicing is modulated by antifungal drugs in the filamentous fungus Neurospora crassa
title_fullStr Pre‐mRNA splicing is modulated by antifungal drugs in the filamentous fungus Neurospora crassa
title_full_unstemmed Pre‐mRNA splicing is modulated by antifungal drugs in the filamentous fungus Neurospora crassa
title_short Pre‐mRNA splicing is modulated by antifungal drugs in the filamentous fungus Neurospora crassa
title_sort pre‐mrna splicing is modulated by antifungal drugs in the filamentous fungus neurospora crassa
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4821360/
https://www.ncbi.nlm.nih.gov/pubmed/27239448
http://dx.doi.org/10.1002/2211-5463.12047
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