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Identification and characterization of the Non-race specific Disease Resistance 1 (NDR1) orthologous protein in coffee
BACKGROUND: Leaf rust, which is caused by the fungus Hemileia vastatrix (Pucciniales), is a devastating disease that affects coffee plants (Coffea arabica L.). Disadvantages that are associated with currently developed phytoprotection approaches have recently led to the search for alternative strate...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3212813/ https://www.ncbi.nlm.nih.gov/pubmed/22023696 http://dx.doi.org/10.1186/1471-2229-11-144 |
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author | Cacas, Jean-Luc Petitot, Anne-Sophie Bernier, Louis Estevan, Joan Conejero, Geneviève Mongrand, Sébastien Fernandez, Diana |
author_facet | Cacas, Jean-Luc Petitot, Anne-Sophie Bernier, Louis Estevan, Joan Conejero, Geneviève Mongrand, Sébastien Fernandez, Diana |
author_sort | Cacas, Jean-Luc |
collection | PubMed |
description | BACKGROUND: Leaf rust, which is caused by the fungus Hemileia vastatrix (Pucciniales), is a devastating disease that affects coffee plants (Coffea arabica L.). Disadvantages that are associated with currently developed phytoprotection approaches have recently led to the search for alternative strategies. These include genetic manipulations that constitutively activate disease resistance signaling pathways. However, molecular actors of such pathways still remain unknown in C. arabica. In this study, we have isolated and characterized the coffee NDR1 gene, whose Arabidopsis ortholog is a well-known master regulator of the hypersensitive response that is dependent on coiled-coil type R-proteins. RESULTS: Two highly homologous cDNAs coding for putative NDR1 proteins were identified and cloned from leaves of coffee plants. One of the candidate coding sequences was then expressed in the Arabidopsis knock-out null mutant ndr1-1. Upon a challenge with a specific strain of the bacterium Pseudomonas syringae (DC3000::AvrRpt2), analysis of both macroscopic symptoms and in planta microbial growth showed that the coffee cDNA was able to restore the resistance phenotype in the mutant genetic background. Thus, the cDNA was dubbed CaNDR1a (standing for Coffea arabica Non-race specific Disease Resistance 1a). Finally, biochemical and microscopy data were obtained that strongly suggest the mechanistic conservation of the NDR1-driven function within coffee and Arabidopsis plants. Using a transient expression system, it was indeed shown that the CaNDR1a protein, like its Arabidopsis counterpart, is localized to the plasma membrane, where it is possibly tethered by means of a GPI anchor. CONCLUSIONS: Our data provide molecular and genetic evidence for the identification of a novel functional NDR1 homolog in plants. As a key regulator initiating hypersensitive signalling pathways, CaNDR1 gene(s) might be target(s) of choice for manipulating the coffee innate immune system and achieving broad spectrum resistance to pathogens. Given the potential conservation of NDR1-dependent defense mechanisms between Arabidopsis and coffee plants, our work also suggests new ways to isolate the as-yet-unidentified R-gene(s) responsible for resistance to H. vastatrix. |
format | Online Article Text |
id | pubmed-3212813 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-32128132011-11-11 Identification and characterization of the Non-race specific Disease Resistance 1 (NDR1) orthologous protein in coffee Cacas, Jean-Luc Petitot, Anne-Sophie Bernier, Louis Estevan, Joan Conejero, Geneviève Mongrand, Sébastien Fernandez, Diana BMC Plant Biol Research Article BACKGROUND: Leaf rust, which is caused by the fungus Hemileia vastatrix (Pucciniales), is a devastating disease that affects coffee plants (Coffea arabica L.). Disadvantages that are associated with currently developed phytoprotection approaches have recently led to the search for alternative strategies. These include genetic manipulations that constitutively activate disease resistance signaling pathways. However, molecular actors of such pathways still remain unknown in C. arabica. In this study, we have isolated and characterized the coffee NDR1 gene, whose Arabidopsis ortholog is a well-known master regulator of the hypersensitive response that is dependent on coiled-coil type R-proteins. RESULTS: Two highly homologous cDNAs coding for putative NDR1 proteins were identified and cloned from leaves of coffee plants. One of the candidate coding sequences was then expressed in the Arabidopsis knock-out null mutant ndr1-1. Upon a challenge with a specific strain of the bacterium Pseudomonas syringae (DC3000::AvrRpt2), analysis of both macroscopic symptoms and in planta microbial growth showed that the coffee cDNA was able to restore the resistance phenotype in the mutant genetic background. Thus, the cDNA was dubbed CaNDR1a (standing for Coffea arabica Non-race specific Disease Resistance 1a). Finally, biochemical and microscopy data were obtained that strongly suggest the mechanistic conservation of the NDR1-driven function within coffee and Arabidopsis plants. Using a transient expression system, it was indeed shown that the CaNDR1a protein, like its Arabidopsis counterpart, is localized to the plasma membrane, where it is possibly tethered by means of a GPI anchor. CONCLUSIONS: Our data provide molecular and genetic evidence for the identification of a novel functional NDR1 homolog in plants. As a key regulator initiating hypersensitive signalling pathways, CaNDR1 gene(s) might be target(s) of choice for manipulating the coffee innate immune system and achieving broad spectrum resistance to pathogens. Given the potential conservation of NDR1-dependent defense mechanisms between Arabidopsis and coffee plants, our work also suggests new ways to isolate the as-yet-unidentified R-gene(s) responsible for resistance to H. vastatrix. BioMed Central 2011-10-24 /pmc/articles/PMC3212813/ /pubmed/22023696 http://dx.doi.org/10.1186/1471-2229-11-144 Text en Copyright ©2011 Cacas et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Cacas, Jean-Luc Petitot, Anne-Sophie Bernier, Louis Estevan, Joan Conejero, Geneviève Mongrand, Sébastien Fernandez, Diana Identification and characterization of the Non-race specific Disease Resistance 1 (NDR1) orthologous protein in coffee |
title | Identification and characterization of the Non-race specific Disease Resistance 1 (NDR1) orthologous protein in coffee |
title_full | Identification and characterization of the Non-race specific Disease Resistance 1 (NDR1) orthologous protein in coffee |
title_fullStr | Identification and characterization of the Non-race specific Disease Resistance 1 (NDR1) orthologous protein in coffee |
title_full_unstemmed | Identification and characterization of the Non-race specific Disease Resistance 1 (NDR1) orthologous protein in coffee |
title_short | Identification and characterization of the Non-race specific Disease Resistance 1 (NDR1) orthologous protein in coffee |
title_sort | identification and characterization of the non-race specific disease resistance 1 (ndr1) orthologous protein in coffee |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3212813/ https://www.ncbi.nlm.nih.gov/pubmed/22023696 http://dx.doi.org/10.1186/1471-2229-11-144 |
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