The Molecular Basis of JAZ-MYC Coupling, a Protein-Protein Interface Essential for Plant Response to Stressors
The jasmonic acid (JA) signaling pathway is one of the primary mechanisms that allow plants to respond to a variety of biotic and abiotic stressors. Within this pathway, the JAZ repressor proteins and the basic helix-loop-helix (bHLH) transcription factor MYC3 play a critical role. JA is a volatile...
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Published in | Frontiers in plant science Vol. 11; p. 1139 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
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20.08.2020
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Abstract | The jasmonic acid (JA) signaling pathway is one of the primary mechanisms that allow plants to respond to a variety of biotic and abiotic stressors. Within this pathway, the JAZ repressor proteins and the basic helix-loop-helix (bHLH) transcription factor MYC3 play a critical role. JA is a volatile organic compound with an essential role in plant immunity. The increase in the concentration of JA leads to the decoupling of the JAZ repressor proteins and the bHLH transcription factor MYC3 causing the induction of genes of interest. The primary goal of this study was to identify the molecular basis of JAZ-MYC coupling. For this purpose, we modeled and validated 12 JAZ-MYC3 3D
in silico
structures and developed a molecular dynamics/machine learning pipeline to obtain two outcomes. First, we calculated the average free binding energy of JAZ-MYC3 complexes, which was predicted to be -10.94 +/-2.67 kJ/mol. Second, we predicted which ones should be the interface residues that make the predominant contribution to the free energy of binding (molecular hotspots). The predicted protein hotspots matched a conserved linear motif SL••FL•••R, which may have a crucial role during MYC3 recognition of JAZ proteins. As a proof of concept, we tested, both
in silico
and
in vitro
, the importance of this motif on PEAPOD (PPD) proteins, which also belong to the TIFY protein family, like the JAZ proteins, but cannot bind to MYC3. By mutating these proteins to match the SL••FL•••R motif, we could force PPDs to bind the MYC3 transcription factor. Taken together, modeling protein-protein interactions and using machine learning will help to find essential motifs and molecular mechanisms in the JA pathway. |
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AbstractList | The jasmonic acid (JA) signaling pathway is one of the primary mechanisms that allow plants to respond to a variety of biotic and abiotic stressors. Within this pathway, the JAZ repressor proteins and the basic helix-loop-helix (bHLH) transcription factor MYC3 play a critical role. JA is a volatile organic compound with an essential role in plant immunity. The increase in the concentration of JA leads to the decoupling of the JAZ repressor proteins and the bHLH transcription factor MYC3 causing the induction of genes of interest. The primary goal of this study was to identify the molecular basis of JAZ-MYC coupling. For this purpose, we modeled and validated 12 JAZ-MYC3 3D in silico structures and developed a molecular dynamics/machine learning pipeline to obtain two outcomes. First, we calculated the average free binding energy of JAZ-MYC3 complexes, which was predicted to be -10.94 +/-2.67 kJ/mol. Second, we predicted which ones should be the interface residues that make the predominant contribution to the free energy of binding (molecular hotspots). The predicted protein hotspots matched a conserved linear motif SL••FL•••R, which may have a crucial role during MYC3 recognition of JAZ proteins. As a proof of concept, we tested, both in silico and in vitro, the importance of this motif on PEAPOD (PPD) proteins, which also belong to the TIFY protein family, like the JAZ proteins, but cannot bind to MYC3. By mutating these proteins to match the SL••FL•••R motif, we could force PPDs to bind the MYC3 transcription factor. Taken together, modeling protein-protein interactions and using machine learning will help to find essential motifs and molecular mechanisms in the JA pathway. The jasmonic acid (JA) signaling pathway is one of the primary mechanisms that allow plants to respond to a variety of biotic and abiotic stressors. Within this pathway, the JAZ repressor proteins and the basic helix-loop-helix (bHLH) transcription factor MYC3 play a critical role. JA is a volatile organic compound with an essential role in plant immunity. The increase in the concentration of JA leads to the decoupling of the JAZ repressor proteins and the bHLH transcription factor MYC3 causing the induction of genes of interest. The primary goal of this study was to identify the molecular basis of JAZ-MYC coupling. For this purpose, we modeled and validated 12 JAZ-MYC3 3D in silico structures and developed a molecular dynamics/machine learning pipeline to obtain two outcomes. First, we calculated the average free binding energy of JAZ-MYC3 complexes, which was predicted to be -10.94 +/-2.67 kJ/mol. Second, we predicted which ones should be the interface residues that make the predominant contribution to the free energy of binding (molecular hotspots). The predicted protein hotspots matched a conserved linear motif SL••FL•••R, which may have a crucial role during MYC3 recognition of JAZ proteins. As a proof of concept, we tested, both in silico and in vitro , the importance of this motif on PEAPOD (PPD) proteins, which also belong to the TIFY protein family, like the JAZ proteins, but cannot bind to MYC3. By mutating these proteins to match the SL••FL•••R motif, we could force PPDs to bind the MYC3 transcription factor. Taken together, modeling protein-protein interactions and using machine learning will help to find essential motifs and molecular mechanisms in the JA pathway. |
Author | Pauwels, Laurens Leon-Reyes, Antonio Oña Chuquimarca, Samara Ayala-Ruano, Sebastián Ángel Méndez, Miguel Goossens, Jonas Goossens, Alain |
AuthorAffiliation | 7 Colegio de Ciencias Biológicas y Ambientales COCIBA, Instituto de Investigaciones Biológicas y Ambientales BIÓSFERA, Universidad San Francisco de Quito USFQ, Campus Cumbayá , Quito , Ecuador 1 Grupo de Química Computacional y Teórica, Departamento de Ingeniería Química, Universidad San Francisco de Quito USFQ, Campus Cumbayá , Quito , Ecuador 2 Instituto de Simulación Computacional (ISC-USFQ), Universidad San Francisco de Quito USFQ , Quito , Ecuador 3 Department of Plant Biotechnology and Bioinformatics, Ghent University , Ghent , Belgium 4 VIB Center for Plant Systems Biology , Ghent , Belgium 8 Department of Biology, The University of North Carolina at Chapel Hill , Chapel Hill, NC , United States 6 Colegio de Ciencias Biológicas y Ambientales COCIBA, Instituto de Microbiología, Universidad San Francisco de Quito USFQ, Campus Cumbayá , Quito , Ecuador 5 Laboratorio de Biotecnología Agrícola y de Alimentos, Ingeniería en Agronomía, Colegio de Ciencias e Ingenierías, Universidad San Franci |
AuthorAffiliation_xml | – name: 3 Department of Plant Biotechnology and Bioinformatics, Ghent University , Ghent , Belgium – name: 4 VIB Center for Plant Systems Biology , Ghent , Belgium – name: 5 Laboratorio de Biotecnología Agrícola y de Alimentos, Ingeniería en Agronomía, Colegio de Ciencias e Ingenierías, Universidad San Francisco de Quito, Campus Cumbayá , Quito , Ecuador – name: 6 Colegio de Ciencias Biológicas y Ambientales COCIBA, Instituto de Microbiología, Universidad San Francisco de Quito USFQ, Campus Cumbayá , Quito , Ecuador – name: 7 Colegio de Ciencias Biológicas y Ambientales COCIBA, Instituto de Investigaciones Biológicas y Ambientales BIÓSFERA, Universidad San Francisco de Quito USFQ, Campus Cumbayá , Quito , Ecuador – name: 2 Instituto de Simulación Computacional (ISC-USFQ), Universidad San Francisco de Quito USFQ , Quito , Ecuador – name: 8 Department of Biology, The University of North Carolina at Chapel Hill , Chapel Hill, NC , United States – name: 1 Grupo de Química Computacional y Teórica, Departamento de Ingeniería Química, Universidad San Francisco de Quito USFQ, Campus Cumbayá , Quito , Ecuador |
Author_xml | – sequence: 1 givenname: Samara surname: Oña Chuquimarca fullname: Oña Chuquimarca, Samara – sequence: 2 givenname: Sebastián surname: Ayala-Ruano fullname: Ayala-Ruano, Sebastián – sequence: 3 givenname: Jonas surname: Goossens fullname: Goossens, Jonas – sequence: 4 givenname: Laurens surname: Pauwels fullname: Pauwels, Laurens – sequence: 5 givenname: Alain surname: Goossens fullname: Goossens, Alain – sequence: 6 givenname: Antonio surname: Leon-Reyes fullname: Leon-Reyes, Antonio – sequence: 7 givenname: Miguel surname: Ángel Méndez fullname: Ángel Méndez, Miguel |
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CitedBy_id | crossref_primary_10_3390_f13050781 crossref_primary_10_3389_fpls_2023_1267107 crossref_primary_10_1016_j_tplants_2020_10_012 crossref_primary_10_3390_plants11131646 crossref_primary_10_55007_dufed_1103457 crossref_primary_10_1111_jipb_13654 crossref_primary_10_3390_ijms24043079 |
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ContentType | Journal Article |
Copyright | Copyright © 2020 Oña Chuquimarca, Ayala-Ruano, Goossens, Pauwels, Goossens, Leon-Reyes and Ángel Méndez 2020 Oña Chuquimarca, Ayala-Ruano, Goossens, Pauwels, Goossens, Leon-Reyes and Ángel Méndez |
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Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Edited by: Hans-Peter Mock, Leibniz Institute of Plant Genetics and Crop Plant Research (IPK), Germany Reviewed by: Tong Zhang, Pacific Northwest National Laboratory (DOE), United States; Jose Valero Galvan, Universidad Autónoma de Ciudad Juárez, Mexico This article was submitted to Plant Proteomics, a section of the journal Frontiers in Plant Science |
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Title | The Molecular Basis of JAZ-MYC Coupling, a Protein-Protein Interface Essential for Plant Response to Stressors |
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