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Unveiling Protein Kinase A Targets in Cryptococcus neoformans Capsule Formation

The protein kinase A (PKA) signal transduction pathway has been associated with pathogenesis in many fungal species. Geddes and colleagues [mBio 7(1):e01862-15, 2016, doi:10.1128/mBio.01862-15] used quantitative proteomics approaches to define proteins with altered abundance during protein kinase A...

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Autor principal: Alspaugh, J. Andrew
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society of Microbiology 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4752596/
https://www.ncbi.nlm.nih.gov/pubmed/26861014
http://dx.doi.org/10.1128/mBio.00021-16
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author Alspaugh, J. Andrew
author_facet Alspaugh, J. Andrew
author_sort Alspaugh, J. Andrew
collection PubMed
description The protein kinase A (PKA) signal transduction pathway has been associated with pathogenesis in many fungal species. Geddes and colleagues [mBio 7(1):e01862-15, 2016, doi:10.1128/mBio.01862-15] used quantitative proteomics approaches to define proteins with altered abundance during protein kinase A (PKA) activation and repression in the opportunistic human fungal pathogen Cryptococcus neoformans. They observed an association between microbial PKA signaling and ubiquitin-proteasome regulation of protein homeostasis. Additionally, they correlated these processes with expression of polysaccharide capsule on the fungal cell surface, the main virulence-associated phenotype in this organism. Not only are their findings important for microbial pathogenesis, but they also support similar associations between human PKA signaling and ubiquitinated protein accumulation in neurodegenerative diseases.
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spelling pubmed-47525962016-02-13 Unveiling Protein Kinase A Targets in Cryptococcus neoformans Capsule Formation Alspaugh, J. Andrew mBio Commentary The protein kinase A (PKA) signal transduction pathway has been associated with pathogenesis in many fungal species. Geddes and colleagues [mBio 7(1):e01862-15, 2016, doi:10.1128/mBio.01862-15] used quantitative proteomics approaches to define proteins with altered abundance during protein kinase A (PKA) activation and repression in the opportunistic human fungal pathogen Cryptococcus neoformans. They observed an association between microbial PKA signaling and ubiquitin-proteasome regulation of protein homeostasis. Additionally, they correlated these processes with expression of polysaccharide capsule on the fungal cell surface, the main virulence-associated phenotype in this organism. Not only are their findings important for microbial pathogenesis, but they also support similar associations between human PKA signaling and ubiquitinated protein accumulation in neurodegenerative diseases. American Society of Microbiology 2016-02-09 /pmc/articles/PMC4752596/ /pubmed/26861014 http://dx.doi.org/10.1128/mBio.00021-16 Text en Copyright © 2016 Alspaugh. http://creativecommons.org/licenses/by-nc-sa/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-ShareAlike 3.0 Unported license (http://creativecommons.org/licenses/by-nc-sa/3.0/) , which permits unrestricted noncommercial use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Commentary
Alspaugh, J. Andrew
Unveiling Protein Kinase A Targets in Cryptococcus neoformans Capsule Formation
title Unveiling Protein Kinase A Targets in Cryptococcus neoformans Capsule Formation
title_full Unveiling Protein Kinase A Targets in Cryptococcus neoformans Capsule Formation
title_fullStr Unveiling Protein Kinase A Targets in Cryptococcus neoformans Capsule Formation
title_full_unstemmed Unveiling Protein Kinase A Targets in Cryptococcus neoformans Capsule Formation
title_short Unveiling Protein Kinase A Targets in Cryptococcus neoformans Capsule Formation
title_sort unveiling protein kinase a targets in cryptococcus neoformans capsule formation
topic Commentary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4752596/
https://www.ncbi.nlm.nih.gov/pubmed/26861014
http://dx.doi.org/10.1128/mBio.00021-16
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