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Extracellular calcium triggers unique transcriptional programs and modulates staurosporine-induced cell death in Neurospora crassa
Alterations in the intracellular levels of calcium are a common response to cell death stimuli in animals and fungi and, particularly, in the Neurospora crassa response to staurosporine. We highlight the importance of the extracellular availability of Ca(2+) for this response. Limitation of the ion...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Shared Science Publishers OG
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5349132/ https://www.ncbi.nlm.nih.gov/pubmed/28357255 http://dx.doi.org/10.15698/mic2014.09.165 |
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author | Gonçalves, A. P. Monteiro, João Lucchi, Chiara Kowbel, David J. Cordeiro, J. M. Correia-de-Sá, Paulo Rigden, Daniel J. Glass, N. L. Videira, Arnaldo |
author_facet | Gonçalves, A. P. Monteiro, João Lucchi, Chiara Kowbel, David J. Cordeiro, J. M. Correia-de-Sá, Paulo Rigden, Daniel J. Glass, N. L. Videira, Arnaldo |
author_sort | Gonçalves, A. P. |
collection | PubMed |
description | Alterations in the intracellular levels of calcium are a common response to cell death stimuli in animals and fungi and, particularly, in the Neurospora crassa response to staurosporine. We highlight the importance of the extracellular availability of Ca(2+) for this response. Limitation of the ion in the culture medium further sensitizes cells to the drug and results in increased accumulation of reactive oxygen species (ROS). Conversely, an approximately 30-fold excess of external Ca(2+) leads to increased drug tolerance and lower ROS generation. In line with this, distinct staurosporine-induced cytosolic Ca(2+) signaling profiles were observed in the absence or presence of excessive external Ca(2+). High-throughput RNA sequencing revealed that different concentrations of extracellular Ca(2+) define distinct transcriptional programs. Our transcriptional profiling also pointed to two putative novel Ca(2+)-binding proteins, encoded by the NCU08524 and NCU06607 genes, and provides a reference dataset for future investigations on the role of Ca(2+) in fungal biology. |
format | Online Article Text |
id | pubmed-5349132 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Shared Science Publishers OG |
record_format | MEDLINE/PubMed |
spelling | pubmed-53491322017-03-29 Extracellular calcium triggers unique transcriptional programs and modulates staurosporine-induced cell death in Neurospora crassa Gonçalves, A. P. Monteiro, João Lucchi, Chiara Kowbel, David J. Cordeiro, J. M. Correia-de-Sá, Paulo Rigden, Daniel J. Glass, N. L. Videira, Arnaldo Microb Cell Microbiology Alterations in the intracellular levels of calcium are a common response to cell death stimuli in animals and fungi and, particularly, in the Neurospora crassa response to staurosporine. We highlight the importance of the extracellular availability of Ca(2+) for this response. Limitation of the ion in the culture medium further sensitizes cells to the drug and results in increased accumulation of reactive oxygen species (ROS). Conversely, an approximately 30-fold excess of external Ca(2+) leads to increased drug tolerance and lower ROS generation. In line with this, distinct staurosporine-induced cytosolic Ca(2+) signaling profiles were observed in the absence or presence of excessive external Ca(2+). High-throughput RNA sequencing revealed that different concentrations of extracellular Ca(2+) define distinct transcriptional programs. Our transcriptional profiling also pointed to two putative novel Ca(2+)-binding proteins, encoded by the NCU08524 and NCU06607 genes, and provides a reference dataset for future investigations on the role of Ca(2+) in fungal biology. Shared Science Publishers OG 2014-08-09 /pmc/articles/PMC5349132/ /pubmed/28357255 http://dx.doi.org/10.15698/mic2014.09.165 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 Gonçalves, A. P. Monteiro, João Lucchi, Chiara Kowbel, David J. Cordeiro, J. M. Correia-de-Sá, Paulo Rigden, Daniel J. Glass, N. L. Videira, Arnaldo Extracellular calcium triggers unique transcriptional programs and modulates staurosporine-induced cell death in Neurospora crassa |
title | Extracellular calcium triggers unique transcriptional programs and
modulates staurosporine-induced cell death in Neurospora
crassa |
title_full | Extracellular calcium triggers unique transcriptional programs and
modulates staurosporine-induced cell death in Neurospora
crassa |
title_fullStr | Extracellular calcium triggers unique transcriptional programs and
modulates staurosporine-induced cell death in Neurospora
crassa |
title_full_unstemmed | Extracellular calcium triggers unique transcriptional programs and
modulates staurosporine-induced cell death in Neurospora
crassa |
title_short | Extracellular calcium triggers unique transcriptional programs and
modulates staurosporine-induced cell death in Neurospora
crassa |
title_sort | extracellular calcium triggers unique transcriptional programs and
modulates staurosporine-induced cell death in neurospora
crassa |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5349132/ https://www.ncbi.nlm.nih.gov/pubmed/28357255 http://dx.doi.org/10.15698/mic2014.09.165 |
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