Cargando…
The Transient Receptor Potential (TRP) Channel Family in Colletotrichum graminicola: A Molecular and Physiological Analysis
Calcium (Ca(2+)) is a universal second messenger in all higher organisms and centrally involved in the launch of responses to environmental stimuli. Ca(2+) signals in the cytosol are initiated by the activation of Ca(2+) channels in the plasma membrane and/or in endomembranes. Yeast (Saccharomyces c...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4928787/ https://www.ncbi.nlm.nih.gov/pubmed/27359114 http://dx.doi.org/10.1371/journal.pone.0158561 |
_version_ | 1782440493797343232 |
---|---|
author | Lange, Mario Weihmann, Fabian Schliebner, Ivo Horbach, Ralf Deising, Holger B. Wirsel, Stefan G. R. Peiter, Edgar |
author_facet | Lange, Mario Weihmann, Fabian Schliebner, Ivo Horbach, Ralf Deising, Holger B. Wirsel, Stefan G. R. Peiter, Edgar |
author_sort | Lange, Mario |
collection | PubMed |
description | Calcium (Ca(2+)) is a universal second messenger in all higher organisms and centrally involved in the launch of responses to environmental stimuli. Ca(2+) signals in the cytosol are initiated by the activation of Ca(2+) channels in the plasma membrane and/or in endomembranes. Yeast (Saccharomyces cerevisiae) contains a Ca(2+)-permeable channel of the TRP family, TRPY1, which is localized in the vacuolar membrane and contributes to cytosolic free Ca(2+) ([Ca(2+)](cyt)) elevations, for example in response to osmotic upshock. A TRPY1 homologue in the rice blast fungus is known to be important for growth and pathogenicity. To determine the role of the TRP channel family in the maize pathogen Colletotrichum graminicola, proteins homologous to TRPY1 were searched. This identified not one, but four genes in the C. graminicola genome, which had putative orthologs in other fungi, and which we named CgTRPF1 through 4. The topology of the CgTRPF proteins resembled that of TRPY1, albeit with a variable number of transmembrane (TM) domains additional to the six-TM-domain core and a diverse arrangement of putatively Ca(2+)-binding acidic motifs. All CgTRPF genes were expressed in axenic culture and throughout the infection of maize. Like TRPY1, all TRPF proteins of C. graminicola were localized intracellularly, albeit three of them were found not in large vacuoles, but co-localized in vesicular structures. Deletion strains for the CgTRPF genes were not altered in processes thought to involve Ca(2+) release from internal stores, i.e. spore germination, the utilization of complex carbon sources, and the generation of tip-focussed [Ca(2+)](cyt) spikes. Heterologous expression of CgTRPF1 through 4 in a tryp1Δ yeast mutant revealed that none of the channels mediated the release of Ca(2+) in response to osmotic upshock. Accordingly, aequorin-based [Ca(2+)](cyt) measurements of C. graminicola showed that in this fungus, osmotic upshock-triggered [Ca(2+)](cyt) elevations were generated entirely by influx of Ca(2+) from the extracellular space. Cgtrpf mutants did not show pathogenicity defects in leaf infection assays. In summary, our study reveals major differences between different fungi in the contribution of TRP channels to Ca(2+)-mediated signal transduction. |
format | Online Article Text |
id | pubmed-4928787 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-49287872016-07-18 The Transient Receptor Potential (TRP) Channel Family in Colletotrichum graminicola: A Molecular and Physiological Analysis Lange, Mario Weihmann, Fabian Schliebner, Ivo Horbach, Ralf Deising, Holger B. Wirsel, Stefan G. R. Peiter, Edgar PLoS One Research Article Calcium (Ca(2+)) is a universal second messenger in all higher organisms and centrally involved in the launch of responses to environmental stimuli. Ca(2+) signals in the cytosol are initiated by the activation of Ca(2+) channels in the plasma membrane and/or in endomembranes. Yeast (Saccharomyces cerevisiae) contains a Ca(2+)-permeable channel of the TRP family, TRPY1, which is localized in the vacuolar membrane and contributes to cytosolic free Ca(2+) ([Ca(2+)](cyt)) elevations, for example in response to osmotic upshock. A TRPY1 homologue in the rice blast fungus is known to be important for growth and pathogenicity. To determine the role of the TRP channel family in the maize pathogen Colletotrichum graminicola, proteins homologous to TRPY1 were searched. This identified not one, but four genes in the C. graminicola genome, which had putative orthologs in other fungi, and which we named CgTRPF1 through 4. The topology of the CgTRPF proteins resembled that of TRPY1, albeit with a variable number of transmembrane (TM) domains additional to the six-TM-domain core and a diverse arrangement of putatively Ca(2+)-binding acidic motifs. All CgTRPF genes were expressed in axenic culture and throughout the infection of maize. Like TRPY1, all TRPF proteins of C. graminicola were localized intracellularly, albeit three of them were found not in large vacuoles, but co-localized in vesicular structures. Deletion strains for the CgTRPF genes were not altered in processes thought to involve Ca(2+) release from internal stores, i.e. spore germination, the utilization of complex carbon sources, and the generation of tip-focussed [Ca(2+)](cyt) spikes. Heterologous expression of CgTRPF1 through 4 in a tryp1Δ yeast mutant revealed that none of the channels mediated the release of Ca(2+) in response to osmotic upshock. Accordingly, aequorin-based [Ca(2+)](cyt) measurements of C. graminicola showed that in this fungus, osmotic upshock-triggered [Ca(2+)](cyt) elevations were generated entirely by influx of Ca(2+) from the extracellular space. Cgtrpf mutants did not show pathogenicity defects in leaf infection assays. In summary, our study reveals major differences between different fungi in the contribution of TRP channels to Ca(2+)-mediated signal transduction. Public Library of Science 2016-06-30 /pmc/articles/PMC4928787/ /pubmed/27359114 http://dx.doi.org/10.1371/journal.pone.0158561 Text en © 2016 Lange et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Lange, Mario Weihmann, Fabian Schliebner, Ivo Horbach, Ralf Deising, Holger B. Wirsel, Stefan G. R. Peiter, Edgar The Transient Receptor Potential (TRP) Channel Family in Colletotrichum graminicola: A Molecular and Physiological Analysis |
title | The Transient Receptor Potential (TRP) Channel Family in Colletotrichum graminicola: A Molecular and Physiological Analysis |
title_full | The Transient Receptor Potential (TRP) Channel Family in Colletotrichum graminicola: A Molecular and Physiological Analysis |
title_fullStr | The Transient Receptor Potential (TRP) Channel Family in Colletotrichum graminicola: A Molecular and Physiological Analysis |
title_full_unstemmed | The Transient Receptor Potential (TRP) Channel Family in Colletotrichum graminicola: A Molecular and Physiological Analysis |
title_short | The Transient Receptor Potential (TRP) Channel Family in Colletotrichum graminicola: A Molecular and Physiological Analysis |
title_sort | transient receptor potential (trp) channel family in colletotrichum graminicola: a molecular and physiological analysis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4928787/ https://www.ncbi.nlm.nih.gov/pubmed/27359114 http://dx.doi.org/10.1371/journal.pone.0158561 |
work_keys_str_mv | AT langemario thetransientreceptorpotentialtrpchannelfamilyincolletotrichumgraminicolaamolecularandphysiologicalanalysis AT weihmannfabian thetransientreceptorpotentialtrpchannelfamilyincolletotrichumgraminicolaamolecularandphysiologicalanalysis AT schliebnerivo thetransientreceptorpotentialtrpchannelfamilyincolletotrichumgraminicolaamolecularandphysiologicalanalysis AT horbachralf thetransientreceptorpotentialtrpchannelfamilyincolletotrichumgraminicolaamolecularandphysiologicalanalysis AT deisingholgerb thetransientreceptorpotentialtrpchannelfamilyincolletotrichumgraminicolaamolecularandphysiologicalanalysis AT wirselstefangr thetransientreceptorpotentialtrpchannelfamilyincolletotrichumgraminicolaamolecularandphysiologicalanalysis AT peiteredgar thetransientreceptorpotentialtrpchannelfamilyincolletotrichumgraminicolaamolecularandphysiologicalanalysis AT langemario transientreceptorpotentialtrpchannelfamilyincolletotrichumgraminicolaamolecularandphysiologicalanalysis AT weihmannfabian transientreceptorpotentialtrpchannelfamilyincolletotrichumgraminicolaamolecularandphysiologicalanalysis AT schliebnerivo transientreceptorpotentialtrpchannelfamilyincolletotrichumgraminicolaamolecularandphysiologicalanalysis AT horbachralf transientreceptorpotentialtrpchannelfamilyincolletotrichumgraminicolaamolecularandphysiologicalanalysis AT deisingholgerb transientreceptorpotentialtrpchannelfamilyincolletotrichumgraminicolaamolecularandphysiologicalanalysis AT wirselstefangr transientreceptorpotentialtrpchannelfamilyincolletotrichumgraminicolaamolecularandphysiologicalanalysis AT peiteredgar transientreceptorpotentialtrpchannelfamilyincolletotrichumgraminicolaamolecularandphysiologicalanalysis |