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Genetic Bypass of Aspergillus nidulans crzA Function in Calcium Homeostasis

After dephosphorylation by the phosphatase calcineurin, the fungal transcription factor CrzA enters the nucleus and activates the transcription of genes responsible for calcium homeostasis and many other calcium-regulated activities. A lack of CrzA confers calcium-sensitivity to the filamentous fung...

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Autores principales: Almeida, Ricardo S., Loss, Omar, Colabardini, Ana Cristina, Brown, Neil Andrew, Bignell, Elaine, Savoldi, Marcela, Pantano, Sergio, Goldman, Maria Helena S., Arst, Herbert N., Goldman, Gustavo H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Genetics Society of America 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3704241/
https://www.ncbi.nlm.nih.gov/pubmed/23665873
http://dx.doi.org/10.1534/g3.113.005983
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author Almeida, Ricardo S.
Loss, Omar
Colabardini, Ana Cristina
Brown, Neil Andrew
Bignell, Elaine
Savoldi, Marcela
Pantano, Sergio
Goldman, Maria Helena S.
Arst, Herbert N.
Goldman, Gustavo H.
author_facet Almeida, Ricardo S.
Loss, Omar
Colabardini, Ana Cristina
Brown, Neil Andrew
Bignell, Elaine
Savoldi, Marcela
Pantano, Sergio
Goldman, Maria Helena S.
Arst, Herbert N.
Goldman, Gustavo H.
author_sort Almeida, Ricardo S.
collection PubMed
description After dephosphorylation by the phosphatase calcineurin, the fungal transcription factor CrzA enters the nucleus and activates the transcription of genes responsible for calcium homeostasis and many other calcium-regulated activities. A lack of CrzA confers calcium-sensitivity to the filamentous fungus Aspergillus nidulans. To further understand calcium signaling in filamentous fungi and to identify genes that interact genetically with CrzA, we selected for mutations that were able to suppress crzAΔ calcium intolerance and identified three genes. Through genetic mapping, gene sequencing, and mutant rescue, we were able to identify these as cnaB (encoding the calcineurin regulatory subunit), folA (encoding an enzyme involved in folic acid biosynthesis, dihydroneopterin aldolase), and scrC (suppression of crzA(-), encoding a hypothetical protein). By using a calcium indicator, Fluo-3, we were able to determine that the wild-type and the suppressor strains were either able to regulate intracellular calcium levels or were able to take up and or store calcium correctly. The increased expression of calcium transporters, pmcA and/or pmcB, in suppressor mutants possibly enabled tolerance to high levels of calcium. Our results suggest that a cnaB suppressor mutation confers calcium tolerance to crzAΔ strains through restoration of calcium homeostasis. These results stress that in A. nidulans there are calcineurin-dependent and CrzA-independent pathways. In addition, it is possible that CrzA is able to contribute to the modulation of folic acid biosynthesis.
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spelling pubmed-37042412013-07-09 Genetic Bypass of Aspergillus nidulans crzA Function in Calcium Homeostasis Almeida, Ricardo S. Loss, Omar Colabardini, Ana Cristina Brown, Neil Andrew Bignell, Elaine Savoldi, Marcela Pantano, Sergio Goldman, Maria Helena S. Arst, Herbert N. Goldman, Gustavo H. G3 (Bethesda) Investigations After dephosphorylation by the phosphatase calcineurin, the fungal transcription factor CrzA enters the nucleus and activates the transcription of genes responsible for calcium homeostasis and many other calcium-regulated activities. A lack of CrzA confers calcium-sensitivity to the filamentous fungus Aspergillus nidulans. To further understand calcium signaling in filamentous fungi and to identify genes that interact genetically with CrzA, we selected for mutations that were able to suppress crzAΔ calcium intolerance and identified three genes. Through genetic mapping, gene sequencing, and mutant rescue, we were able to identify these as cnaB (encoding the calcineurin regulatory subunit), folA (encoding an enzyme involved in folic acid biosynthesis, dihydroneopterin aldolase), and scrC (suppression of crzA(-), encoding a hypothetical protein). By using a calcium indicator, Fluo-3, we were able to determine that the wild-type and the suppressor strains were either able to regulate intracellular calcium levels or were able to take up and or store calcium correctly. The increased expression of calcium transporters, pmcA and/or pmcB, in suppressor mutants possibly enabled tolerance to high levels of calcium. Our results suggest that a cnaB suppressor mutation confers calcium tolerance to crzAΔ strains through restoration of calcium homeostasis. These results stress that in A. nidulans there are calcineurin-dependent and CrzA-independent pathways. In addition, it is possible that CrzA is able to contribute to the modulation of folic acid biosynthesis. Genetics Society of America 2013-07-01 /pmc/articles/PMC3704241/ /pubmed/23665873 http://dx.doi.org/10.1534/g3.113.005983 Text en Copyright © 2013 Almeida et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Unported License (http://creativecommons.org/licenses/by/3.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Investigations
Almeida, Ricardo S.
Loss, Omar
Colabardini, Ana Cristina
Brown, Neil Andrew
Bignell, Elaine
Savoldi, Marcela
Pantano, Sergio
Goldman, Maria Helena S.
Arst, Herbert N.
Goldman, Gustavo H.
Genetic Bypass of Aspergillus nidulans crzA Function in Calcium Homeostasis
title Genetic Bypass of Aspergillus nidulans crzA Function in Calcium Homeostasis
title_full Genetic Bypass of Aspergillus nidulans crzA Function in Calcium Homeostasis
title_fullStr Genetic Bypass of Aspergillus nidulans crzA Function in Calcium Homeostasis
title_full_unstemmed Genetic Bypass of Aspergillus nidulans crzA Function in Calcium Homeostasis
title_short Genetic Bypass of Aspergillus nidulans crzA Function in Calcium Homeostasis
title_sort genetic bypass of aspergillus nidulans crza function in calcium homeostasis
topic Investigations
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3704241/
https://www.ncbi.nlm.nih.gov/pubmed/23665873
http://dx.doi.org/10.1534/g3.113.005983
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