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Ras signalling in pathogenic yeasts

The small GTPase Ras acts as a master regulator of growth, stress response and cell death in eukaryotic cells. The control of Ras activity is fundamental, as highlighted by the oncogenic properties of constitutive forms of Ras proteins. Ras also plays a crucial role in the pathogenicity of fungal pa...

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Autores principales: Pentland, Daniel R., Piper-Brown, Elliot, Mühlschlegel, Fritz A., Gourlay, Campbell W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Shared Science Publishers OG 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5798406/
https://www.ncbi.nlm.nih.gov/pubmed/29417055
http://dx.doi.org/10.15698/mic2018.02.612
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author Pentland, Daniel R.
Piper-Brown, Elliot
Mühlschlegel, Fritz A.
Gourlay, Campbell W.
author_facet Pentland, Daniel R.
Piper-Brown, Elliot
Mühlschlegel, Fritz A.
Gourlay, Campbell W.
author_sort Pentland, Daniel R.
collection PubMed
description The small GTPase Ras acts as a master regulator of growth, stress response and cell death in eukaryotic cells. The control of Ras activity is fundamental, as highlighted by the oncogenic properties of constitutive forms of Ras proteins. Ras also plays a crucial role in the pathogenicity of fungal pathogens where it has been found to regulate a number of adaptions required for virulence. The importance of Ras in fungal disease raises the possibility that it may provide a useful target for the development of new treatments at a time when resistance to available antifungals is increasing. New findings suggest that important regulatory sequences found within fungal Ras proteins that are not conserved may prove useful in the development of new antifungals. Here we review the roles of Ras protein function and signalling in the major human yeast pathogens Candida albicans and Cryptococcus neoformans and discuss the potential for targeting Ras as a novel approach to anti-fungal therapy.
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spelling pubmed-57984062018-02-07 Ras signalling in pathogenic yeasts Pentland, Daniel R. Piper-Brown, Elliot Mühlschlegel, Fritz A. Gourlay, Campbell W. Microb Cell Microbiology The small GTPase Ras acts as a master regulator of growth, stress response and cell death in eukaryotic cells. The control of Ras activity is fundamental, as highlighted by the oncogenic properties of constitutive forms of Ras proteins. Ras also plays a crucial role in the pathogenicity of fungal pathogens where it has been found to regulate a number of adaptions required for virulence. The importance of Ras in fungal disease raises the possibility that it may provide a useful target for the development of new treatments at a time when resistance to available antifungals is increasing. New findings suggest that important regulatory sequences found within fungal Ras proteins that are not conserved may prove useful in the development of new antifungals. Here we review the roles of Ras protein function and signalling in the major human yeast pathogens Candida albicans and Cryptococcus neoformans and discuss the potential for targeting Ras as a novel approach to anti-fungal therapy. Shared Science Publishers OG 2017-12-18 /pmc/articles/PMC5798406/ /pubmed/29417055 http://dx.doi.org/10.15698/mic2018.02.612 Text en https://creativecommons.org/licenses/by/4.0/ This is an open-access article released under the terms of the Creative Commons Attribution (CC BY) license, which allows the unrestricted use, distribution, and reproduction in any medium, provided the original author and source are acknowledged.
spellingShingle Microbiology
Pentland, Daniel R.
Piper-Brown, Elliot
Mühlschlegel, Fritz A.
Gourlay, Campbell W.
Ras signalling in pathogenic yeasts
title Ras signalling in pathogenic yeasts
title_full Ras signalling in pathogenic yeasts
title_fullStr Ras signalling in pathogenic yeasts
title_full_unstemmed Ras signalling in pathogenic yeasts
title_short Ras signalling in pathogenic yeasts
title_sort ras signalling in pathogenic yeasts
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5798406/
https://www.ncbi.nlm.nih.gov/pubmed/29417055
http://dx.doi.org/10.15698/mic2018.02.612
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