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A p53-like transcription factor similar to Ndt80 controls the response to nutrient stress in the filamentous fungus, Aspergillus nidulans
The Aspergillus nidulans xprG gene encodes a putative transcriptional activator that is a member of the Ndt80 family in the p53-like superfamily of proteins. Previous studies have shown that XprG controls the production of extracellular proteases in response to starvation. We undertook transcription...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
F1000Research
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3821154/ https://www.ncbi.nlm.nih.gov/pubmed/24358888 http://dx.doi.org/10.12688/f1000research.2-72.v1 |
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author | Katz, Margaret E Braunberger, Kathryn Yi, Gauncai Cooper, Sarah Nonhebel, Heather M Gondro, Cedric |
author_facet | Katz, Margaret E Braunberger, Kathryn Yi, Gauncai Cooper, Sarah Nonhebel, Heather M Gondro, Cedric |
author_sort | Katz, Margaret E |
collection | PubMed |
description | The Aspergillus nidulans xprG gene encodes a putative transcriptional activator that is a member of the Ndt80 family in the p53-like superfamily of proteins. Previous studies have shown that XprG controls the production of extracellular proteases in response to starvation. We undertook transcriptional profiling to investigate whether XprG has a wider role as a global regulator of the carbon nutrient stress response. Our microarray data showed that the expression of a large number of genes, including genes involved in secondary metabolism, development, high-affinity glucose uptake and autolysis, were altered in an xprG Δ null mutant. Many of these genes are known to be regulated in response to carbon starvation. We confirmed that sterigmatocystin and penicillin production is reduced in xprG (-) mutants. The loss of fungal mass and secretion of pigments that accompanies fungal autolysis in response to nutrient depletion was accelerated in an xprG1 gain-of-function mutant and decreased or absent in an xprG (-) mutant. The results support the hypothesis that XprG plays a major role in the response to carbon limitation and that nutrient sensing may represent one of the ancestral roles for the p53-like superfamily. Disruption of the AN6015 gene, which encodes a second Ndt80-like protein, showed that it is required for sexual reproduction in A. nidulans. |
format | Online Article Text |
id | pubmed-3821154 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | F1000Research |
record_format | MEDLINE/PubMed |
spelling | pubmed-38211542013-12-05 A p53-like transcription factor similar to Ndt80 controls the response to nutrient stress in the filamentous fungus, Aspergillus nidulans Katz, Margaret E Braunberger, Kathryn Yi, Gauncai Cooper, Sarah Nonhebel, Heather M Gondro, Cedric F1000Res Research Article The Aspergillus nidulans xprG gene encodes a putative transcriptional activator that is a member of the Ndt80 family in the p53-like superfamily of proteins. Previous studies have shown that XprG controls the production of extracellular proteases in response to starvation. We undertook transcriptional profiling to investigate whether XprG has a wider role as a global regulator of the carbon nutrient stress response. Our microarray data showed that the expression of a large number of genes, including genes involved in secondary metabolism, development, high-affinity glucose uptake and autolysis, were altered in an xprG Δ null mutant. Many of these genes are known to be regulated in response to carbon starvation. We confirmed that sterigmatocystin and penicillin production is reduced in xprG (-) mutants. The loss of fungal mass and secretion of pigments that accompanies fungal autolysis in response to nutrient depletion was accelerated in an xprG1 gain-of-function mutant and decreased or absent in an xprG (-) mutant. The results support the hypothesis that XprG plays a major role in the response to carbon limitation and that nutrient sensing may represent one of the ancestral roles for the p53-like superfamily. Disruption of the AN6015 gene, which encodes a second Ndt80-like protein, showed that it is required for sexual reproduction in A. nidulans. F1000Research 2013-03-04 /pmc/articles/PMC3821154/ /pubmed/24358888 http://dx.doi.org/10.12688/f1000research.2-72.v1 Text en Copyright: © 2013 Katz ME et al. http://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/publicdomain/zero/1.0/ Data associated with the article are available under the terms of the Creative Commons Zero "No rights reserved" data waiver (CC0 1.0 Public domain dedication). |
spellingShingle | Research Article Katz, Margaret E Braunberger, Kathryn Yi, Gauncai Cooper, Sarah Nonhebel, Heather M Gondro, Cedric A p53-like transcription factor similar to Ndt80 controls the response to nutrient stress in the filamentous fungus, Aspergillus nidulans |
title | A p53-like transcription factor similar to Ndt80 controls the response to nutrient stress in the filamentous fungus,
Aspergillus nidulans
|
title_full | A p53-like transcription factor similar to Ndt80 controls the response to nutrient stress in the filamentous fungus,
Aspergillus nidulans
|
title_fullStr | A p53-like transcription factor similar to Ndt80 controls the response to nutrient stress in the filamentous fungus,
Aspergillus nidulans
|
title_full_unstemmed | A p53-like transcription factor similar to Ndt80 controls the response to nutrient stress in the filamentous fungus,
Aspergillus nidulans
|
title_short | A p53-like transcription factor similar to Ndt80 controls the response to nutrient stress in the filamentous fungus,
Aspergillus nidulans
|
title_sort | p53-like transcription factor similar to ndt80 controls the response to nutrient stress in the filamentous fungus,
aspergillus nidulans |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3821154/ https://www.ncbi.nlm.nih.gov/pubmed/24358888 http://dx.doi.org/10.12688/f1000research.2-72.v1 |
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