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Differential expression of CPKs and cytosolic Ca(2+) variation in resistant and susceptible apple cultivars (Malus x domestica) in response to the pathogen Erwinia amylovora and mechanical wounding

BACKGROUND: Plant calcium (Ca(2+)) signals are involved in a wide array of intracellular signalling pathways following pathogen invasion. Ca(2+)-binding sensory proteins such as Ca(2+)-dependent protein kinases (CPKs) have been predicted to mediate signalling following Ca(2+) influx after pathogen i...

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Autores principales: Kanchiswamy, Chidananda Nagamangala, Mohanta, Tapan Kumar, Capuzzo, Andrea, Occhipinti, Andrea, Verrillo, Francesca, Maffei, Massimo E, Malnoy, Mickael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3840711/
https://www.ncbi.nlm.nih.gov/pubmed/24192013
http://dx.doi.org/10.1186/1471-2164-14-760
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author Kanchiswamy, Chidananda Nagamangala
Mohanta, Tapan Kumar
Capuzzo, Andrea
Occhipinti, Andrea
Verrillo, Francesca
Maffei, Massimo E
Malnoy, Mickael
author_facet Kanchiswamy, Chidananda Nagamangala
Mohanta, Tapan Kumar
Capuzzo, Andrea
Occhipinti, Andrea
Verrillo, Francesca
Maffei, Massimo E
Malnoy, Mickael
author_sort Kanchiswamy, Chidananda Nagamangala
collection PubMed
description BACKGROUND: Plant calcium (Ca(2+)) signals are involved in a wide array of intracellular signalling pathways following pathogen invasion. Ca(2+)-binding sensory proteins such as Ca(2+)-dependent protein kinases (CPKs) have been predicted to mediate signalling following Ca(2+) influx after pathogen infection. However, to date this prediction has remained elusive. RESULTS: We conducted a genome-wide identification of the Malus x domestica CPK (MdCPK) gene family and identified 30 CPK genes. Comparative phylogenetic analysis of Malus CPKs with CPKs of Arabidopsis thaliana (AtCPKs), Oryza sativa (OsCPKs), Populous trichocarpa (PtCPKs) and Zea mays (ZmCPKs) revealed four different groups. From the phylogenetic tree, we found that MdCPKs are closely related to AtCPKs and PtCPKs rather than OsCPKs and ZmCPKs, indicating their dicot-specific origin. Furthermore, comparative quantitative real time PCR and intracellular cytosolic calcium ([Ca(2+)](cyt)) analysis were carried out on fire blight resistant and susceptible M. x domestica apple cultivars following infection with a pathogen (Erwinia amylovora) and/or mechanical damage. Calcium analysis showed an increased [Ca(2+)](cyt) over time in resistant cultivars as compared to susceptible cultivars. Gene expression studies showed that 11 out of the 30 MdCPKs were differentially expressed following pathogen infection. CONCLUSIONS: We studied the genome-wide analysis of MdCPK gene family in Malus x domestica and analyzed their differential gene expression along with cytosolic calcium variation upon pathogen infection. There was a striking difference in MdCPKs gene expressions and [Ca(2+)](cyt) variations between resistant and susceptible M. x domestica cultivars in response to E. amylovora and mechanical wounding. Our genomic and bioinformatic analysis provided an important insight about the role of MdCPKs in modulating defence responses in susceptible and resistant apple cultivars. It also provided further information on early signalling and downstream signalling cascades in response to pathogenic and mechanical stress.
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spelling pubmed-38407112013-11-27 Differential expression of CPKs and cytosolic Ca(2+) variation in resistant and susceptible apple cultivars (Malus x domestica) in response to the pathogen Erwinia amylovora and mechanical wounding Kanchiswamy, Chidananda Nagamangala Mohanta, Tapan Kumar Capuzzo, Andrea Occhipinti, Andrea Verrillo, Francesca Maffei, Massimo E Malnoy, Mickael BMC Genomics Research Article BACKGROUND: Plant calcium (Ca(2+)) signals are involved in a wide array of intracellular signalling pathways following pathogen invasion. Ca(2+)-binding sensory proteins such as Ca(2+)-dependent protein kinases (CPKs) have been predicted to mediate signalling following Ca(2+) influx after pathogen infection. However, to date this prediction has remained elusive. RESULTS: We conducted a genome-wide identification of the Malus x domestica CPK (MdCPK) gene family and identified 30 CPK genes. Comparative phylogenetic analysis of Malus CPKs with CPKs of Arabidopsis thaliana (AtCPKs), Oryza sativa (OsCPKs), Populous trichocarpa (PtCPKs) and Zea mays (ZmCPKs) revealed four different groups. From the phylogenetic tree, we found that MdCPKs are closely related to AtCPKs and PtCPKs rather than OsCPKs and ZmCPKs, indicating their dicot-specific origin. Furthermore, comparative quantitative real time PCR and intracellular cytosolic calcium ([Ca(2+)](cyt)) analysis were carried out on fire blight resistant and susceptible M. x domestica apple cultivars following infection with a pathogen (Erwinia amylovora) and/or mechanical damage. Calcium analysis showed an increased [Ca(2+)](cyt) over time in resistant cultivars as compared to susceptible cultivars. Gene expression studies showed that 11 out of the 30 MdCPKs were differentially expressed following pathogen infection. CONCLUSIONS: We studied the genome-wide analysis of MdCPK gene family in Malus x domestica and analyzed their differential gene expression along with cytosolic calcium variation upon pathogen infection. There was a striking difference in MdCPKs gene expressions and [Ca(2+)](cyt) variations between resistant and susceptible M. x domestica cultivars in response to E. amylovora and mechanical wounding. Our genomic and bioinformatic analysis provided an important insight about the role of MdCPKs in modulating defence responses in susceptible and resistant apple cultivars. It also provided further information on early signalling and downstream signalling cascades in response to pathogenic and mechanical stress. BioMed Central 2013-11-05 /pmc/articles/PMC3840711/ /pubmed/24192013 http://dx.doi.org/10.1186/1471-2164-14-760 Text en Copyright © 2013 Kanchiswamy 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
Kanchiswamy, Chidananda Nagamangala
Mohanta, Tapan Kumar
Capuzzo, Andrea
Occhipinti, Andrea
Verrillo, Francesca
Maffei, Massimo E
Malnoy, Mickael
Differential expression of CPKs and cytosolic Ca(2+) variation in resistant and susceptible apple cultivars (Malus x domestica) in response to the pathogen Erwinia amylovora and mechanical wounding
title Differential expression of CPKs and cytosolic Ca(2+) variation in resistant and susceptible apple cultivars (Malus x domestica) in response to the pathogen Erwinia amylovora and mechanical wounding
title_full Differential expression of CPKs and cytosolic Ca(2+) variation in resistant and susceptible apple cultivars (Malus x domestica) in response to the pathogen Erwinia amylovora and mechanical wounding
title_fullStr Differential expression of CPKs and cytosolic Ca(2+) variation in resistant and susceptible apple cultivars (Malus x domestica) in response to the pathogen Erwinia amylovora and mechanical wounding
title_full_unstemmed Differential expression of CPKs and cytosolic Ca(2+) variation in resistant and susceptible apple cultivars (Malus x domestica) in response to the pathogen Erwinia amylovora and mechanical wounding
title_short Differential expression of CPKs and cytosolic Ca(2+) variation in resistant and susceptible apple cultivars (Malus x domestica) in response to the pathogen Erwinia amylovora and mechanical wounding
title_sort differential expression of cpks and cytosolic ca(2+) variation in resistant and susceptible apple cultivars (malus x domestica) in response to the pathogen erwinia amylovora and mechanical wounding
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3840711/
https://www.ncbi.nlm.nih.gov/pubmed/24192013
http://dx.doi.org/10.1186/1471-2164-14-760
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