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The Fungal Cell Death Regulator czt-1 Is Allelic to acr-3

Fungal infections have far-reaching implications that range from severe human disease to a panoply of disruptive agricultural and ecological effects, making it imperative to identify and understand the molecular pathways governing the response to antifungal compounds. In this context, CZT-1 (cell de...

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Autores principales: Gonçalves, A. Pedro, McCluskey, Kevin, Glass, N. Louise, Videira, Arnaldo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6958467/
https://www.ncbi.nlm.nih.gov/pubmed/31817728
http://dx.doi.org/10.3390/jof5040114
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author Gonçalves, A. Pedro
McCluskey, Kevin
Glass, N. Louise
Videira, Arnaldo
author_facet Gonçalves, A. Pedro
McCluskey, Kevin
Glass, N. Louise
Videira, Arnaldo
author_sort Gonçalves, A. Pedro
collection PubMed
description Fungal infections have far-reaching implications that range from severe human disease to a panoply of disruptive agricultural and ecological effects, making it imperative to identify and understand the molecular pathways governing the response to antifungal compounds. In this context, CZT-1 (cell death-activated zinc cluster transcription factor) functions as a master regulator of cell death and drug susceptibility in Neurospora crassa. Here we provide evidence indicating that czt-1 is allelic to acr-3, a previously described locus that we now found to harbor a point mutation in its coding sequence. This nonsynonymous amino acid substitution in a low complexity region of CZT-1/ACR-3 caused a robust gain-of-function that led to reduced sensitivity to acriflavine and staurosporine, and increased expression of the drug efflux pump abc-3. Thus, accumulating evidence shows that CZT-1 is an important broad regulator of the cellular response to various antifungal compounds that appear to share common molecular targets.
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spelling pubmed-69584672020-01-23 The Fungal Cell Death Regulator czt-1 Is Allelic to acr-3 Gonçalves, A. Pedro McCluskey, Kevin Glass, N. Louise Videira, Arnaldo J Fungi (Basel) Communication Fungal infections have far-reaching implications that range from severe human disease to a panoply of disruptive agricultural and ecological effects, making it imperative to identify and understand the molecular pathways governing the response to antifungal compounds. In this context, CZT-1 (cell death-activated zinc cluster transcription factor) functions as a master regulator of cell death and drug susceptibility in Neurospora crassa. Here we provide evidence indicating that czt-1 is allelic to acr-3, a previously described locus that we now found to harbor a point mutation in its coding sequence. This nonsynonymous amino acid substitution in a low complexity region of CZT-1/ACR-3 caused a robust gain-of-function that led to reduced sensitivity to acriflavine and staurosporine, and increased expression of the drug efflux pump abc-3. Thus, accumulating evidence shows that CZT-1 is an important broad regulator of the cellular response to various antifungal compounds that appear to share common molecular targets. MDPI 2019-12-06 /pmc/articles/PMC6958467/ /pubmed/31817728 http://dx.doi.org/10.3390/jof5040114 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Communication
Gonçalves, A. Pedro
McCluskey, Kevin
Glass, N. Louise
Videira, Arnaldo
The Fungal Cell Death Regulator czt-1 Is Allelic to acr-3
title The Fungal Cell Death Regulator czt-1 Is Allelic to acr-3
title_full The Fungal Cell Death Regulator czt-1 Is Allelic to acr-3
title_fullStr The Fungal Cell Death Regulator czt-1 Is Allelic to acr-3
title_full_unstemmed The Fungal Cell Death Regulator czt-1 Is Allelic to acr-3
title_short The Fungal Cell Death Regulator czt-1 Is Allelic to acr-3
title_sort fungal cell death regulator czt-1 is allelic to acr-3
topic Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6958467/
https://www.ncbi.nlm.nih.gov/pubmed/31817728
http://dx.doi.org/10.3390/jof5040114
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