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The pathogenesis-related protein PR-4b from Theobroma cacao presents RNase activity, Ca(2+) and Mg(2+) dependent-DNase activity and antifungal action on Moniliophthora perniciosa

BACKGROUND: The production and accumulation of pathogenesis-related proteins (PR proteins) in plants in response to biotic or abiotic stresses is well known and is considered as a crucial mechanism for plant defense. A pathogenesis-related protein 4 cDNA was identified from a cacao-Moniliophthora pe...

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Autores principales: Pereira Menezes, Sara, de Andrade Silva, Edson Mario, Matos Lima, Eline, Oliveira de Sousa, Aurizângela, Silva Andrade, Bruno, Santos Lima Lemos, Livia, Peres Gramacho, Karina, da Silva Gesteira, Abelmon, Pirovani, Carlos Priminho, Micheli, Fabienne
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4079191/
https://www.ncbi.nlm.nih.gov/pubmed/24920373
http://dx.doi.org/10.1186/1471-2229-14-161
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author Pereira Menezes, Sara
de Andrade Silva, Edson Mario
Matos Lima, Eline
Oliveira de Sousa, Aurizângela
Silva Andrade, Bruno
Santos Lima Lemos, Livia
Peres Gramacho, Karina
da Silva Gesteira, Abelmon
Pirovani, Carlos Priminho
Micheli, Fabienne
author_facet Pereira Menezes, Sara
de Andrade Silva, Edson Mario
Matos Lima, Eline
Oliveira de Sousa, Aurizângela
Silva Andrade, Bruno
Santos Lima Lemos, Livia
Peres Gramacho, Karina
da Silva Gesteira, Abelmon
Pirovani, Carlos Priminho
Micheli, Fabienne
author_sort Pereira Menezes, Sara
collection PubMed
description BACKGROUND: The production and accumulation of pathogenesis-related proteins (PR proteins) in plants in response to biotic or abiotic stresses is well known and is considered as a crucial mechanism for plant defense. A pathogenesis-related protein 4 cDNA was identified from a cacao-Moniliophthora perniciosa interaction cDNA library and named TcPR-4b. RESULTS: TcPR-4b presents a Barwin domain with six conserved cysteine residues, but lacks the chitin-binding site. Molecular modeling of TcPR-4b confirmed the importance of the cysteine residues to maintain the protein structure, and of several conserved amino acids for the catalytic activity. In the cacao genome, TcPR-4b belonged to a small multigene family organized mainly on chromosome 5. TcPR-4b RT-qPCR analysis in resistant and susceptible cacao plants infected by M. perniciosa showed an increase of expression at 48 hours after infection (hai) in both cacao genotypes. After the initial stage (24-72 hai), the TcPR-4b expression was observed at all times in the resistant genotypes, while in the susceptible one the expression was concentrated at the final stages of infection (45-90 days after infection). The recombinant TcPR-4b protein showed RNase, and bivalent ions dependent-DNase activity, but no chitinase activity. Moreover, TcPR-4b presented antifungal action against M. perniciosa, and the reduction of M. perniciosa survival was related to ROS production in fungal hyphae. CONCLUSION: To our knowledge, this is the first report of a PR-4 showing simultaneously RNase, DNase and antifungal properties, but no chitinase activity. Moreover, we showed that the antifungal activity of TcPR-4b is directly related to RNase function. In cacao, TcPR-4b nuclease activities may be related to the establishment and maintenance of resistance, and to the PCD mechanism, in resistant and susceptible cacao genotypes, respectively.
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spelling pubmed-40791912014-07-03 The pathogenesis-related protein PR-4b from Theobroma cacao presents RNase activity, Ca(2+) and Mg(2+) dependent-DNase activity and antifungal action on Moniliophthora perniciosa Pereira Menezes, Sara de Andrade Silva, Edson Mario Matos Lima, Eline Oliveira de Sousa, Aurizângela Silva Andrade, Bruno Santos Lima Lemos, Livia Peres Gramacho, Karina da Silva Gesteira, Abelmon Pirovani, Carlos Priminho Micheli, Fabienne BMC Plant Biol Research Article BACKGROUND: The production and accumulation of pathogenesis-related proteins (PR proteins) in plants in response to biotic or abiotic stresses is well known and is considered as a crucial mechanism for plant defense. A pathogenesis-related protein 4 cDNA was identified from a cacao-Moniliophthora perniciosa interaction cDNA library and named TcPR-4b. RESULTS: TcPR-4b presents a Barwin domain with six conserved cysteine residues, but lacks the chitin-binding site. Molecular modeling of TcPR-4b confirmed the importance of the cysteine residues to maintain the protein structure, and of several conserved amino acids for the catalytic activity. In the cacao genome, TcPR-4b belonged to a small multigene family organized mainly on chromosome 5. TcPR-4b RT-qPCR analysis in resistant and susceptible cacao plants infected by M. perniciosa showed an increase of expression at 48 hours after infection (hai) in both cacao genotypes. After the initial stage (24-72 hai), the TcPR-4b expression was observed at all times in the resistant genotypes, while in the susceptible one the expression was concentrated at the final stages of infection (45-90 days after infection). The recombinant TcPR-4b protein showed RNase, and bivalent ions dependent-DNase activity, but no chitinase activity. Moreover, TcPR-4b presented antifungal action against M. perniciosa, and the reduction of M. perniciosa survival was related to ROS production in fungal hyphae. CONCLUSION: To our knowledge, this is the first report of a PR-4 showing simultaneously RNase, DNase and antifungal properties, but no chitinase activity. Moreover, we showed that the antifungal activity of TcPR-4b is directly related to RNase function. In cacao, TcPR-4b nuclease activities may be related to the establishment and maintenance of resistance, and to the PCD mechanism, in resistant and susceptible cacao genotypes, respectively. BioMed Central 2014-06-11 /pmc/articles/PMC4079191/ /pubmed/24920373 http://dx.doi.org/10.1186/1471-2229-14-161 Text en Copyright © 2014 Pereira Menezes et al.; licensee BioMed Central Ltd. 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 work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Pereira Menezes, Sara
de Andrade Silva, Edson Mario
Matos Lima, Eline
Oliveira de Sousa, Aurizângela
Silva Andrade, Bruno
Santos Lima Lemos, Livia
Peres Gramacho, Karina
da Silva Gesteira, Abelmon
Pirovani, Carlos Priminho
Micheli, Fabienne
The pathogenesis-related protein PR-4b from Theobroma cacao presents RNase activity, Ca(2+) and Mg(2+) dependent-DNase activity and antifungal action on Moniliophthora perniciosa
title The pathogenesis-related protein PR-4b from Theobroma cacao presents RNase activity, Ca(2+) and Mg(2+) dependent-DNase activity and antifungal action on Moniliophthora perniciosa
title_full The pathogenesis-related protein PR-4b from Theobroma cacao presents RNase activity, Ca(2+) and Mg(2+) dependent-DNase activity and antifungal action on Moniliophthora perniciosa
title_fullStr The pathogenesis-related protein PR-4b from Theobroma cacao presents RNase activity, Ca(2+) and Mg(2+) dependent-DNase activity and antifungal action on Moniliophthora perniciosa
title_full_unstemmed The pathogenesis-related protein PR-4b from Theobroma cacao presents RNase activity, Ca(2+) and Mg(2+) dependent-DNase activity and antifungal action on Moniliophthora perniciosa
title_short The pathogenesis-related protein PR-4b from Theobroma cacao presents RNase activity, Ca(2+) and Mg(2+) dependent-DNase activity and antifungal action on Moniliophthora perniciosa
title_sort pathogenesis-related protein pr-4b from theobroma cacao presents rnase activity, ca(2+) and mg(2+) dependent-dnase activity and antifungal action on moniliophthora perniciosa
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4079191/
https://www.ncbi.nlm.nih.gov/pubmed/24920373
http://dx.doi.org/10.1186/1471-2229-14-161
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