Serveur d'exploration sur les récepteurs immunitaires végétaux

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Differential activities of maize Plant Elicitor Peptides as mediators of immune signaling and herbivore resistance.

Identifieur interne : 000179 ( Main/Exploration ); précédent : 000178; suivant : 000180

Differential activities of maize Plant Elicitor Peptides as mediators of immune signaling and herbivore resistance.

Auteurs : Elly Poretsky [États-Unis] ; Keini Dressano [États-Unis] ; Philipp Weckwerth [États-Unis] ; Miguel Ruiz [États-Unis] ; Si Nian Char [États-Unis] ; Shi Da [États-Unis] ; Ruben Abagyan [États-Unis] ; Bing Yang [États-Unis] ; Alisa Huffaker [États-Unis]

Source :

RBID : pubmed:33058410

Abstract

Plant Elicitor Peptides (Peps) are conserved regulators of defense responses and models for the study of Damage-Associated Molecular Pattern (DAMP)-induced immunity. Although present as multigene families in most species, the functional relevance of these multigene families remains largely undefined. While Arabidopsis Peps appear largely redundant in function, previous work examining Pep-induced responses in maize implied specificity of function. To better define function of individual ZmPeps and their cognate ZmPEPR receptors, activities were examined by assessing changes in defense-associated phytohormones, specialized metabolites and global gene expression patterns, in combination with heterologous expression assays and analyses of CRISPR/Cas9-generated knockout plants. Beyond simply delineating individual ZmPep and ZmPEPR activities, these experiments led to a number of new insights into Pep signaling mechanisms. ZmPROPEP and other Poaceous precursors were found to contain multiple active Peps, a phenomenon not previously observed for this family. In all, seven new ZmPeps were identified and the peptides were found to have specific activities defined by relative magnitude of response output rather than by uniqueness. A striking correlation between individual ZmPep-elicited changes in levels of jasmonic acid and ethylene and the magnitude of induced defense responses was observed, indicating that collectively ZmPeps may regulate immune output through rheostat-like tuning of phytohormone levels. Peptide structure-function studies and ligand-receptor modeling revealed structural features critical to ZmPep function and led to identification of ZmPep5a as a potential antagonist peptide able to competitively inhibit activity of other ZmPeps, a regulatory mechanism not previously observed for this family.

DOI: 10.1111/tpj.15022
PubMed: 33058410


Affiliations:


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<div type="abstract" xml:lang="en">Plant Elicitor Peptides (Peps) are conserved regulators of defense responses and models for the study of Damage-Associated Molecular Pattern (DAMP)-induced immunity. Although present as multigene families in most species, the functional relevance of these multigene families remains largely undefined. While Arabidopsis Peps appear largely redundant in function, previous work examining Pep-induced responses in maize implied specificity of function. To better define function of individual ZmPeps and their cognate ZmPEPR receptors, activities were examined by assessing changes in defense-associated phytohormones, specialized metabolites and global gene expression patterns, in combination with heterologous expression assays and analyses of CRISPR/Cas9-generated knockout plants. Beyond simply delineating individual ZmPep and ZmPEPR activities, these experiments led to a number of new insights into Pep signaling mechanisms. ZmPROPEP and other Poaceous precursors were found to contain multiple active Peps, a phenomenon not previously observed for this family. In all, seven new ZmPeps were identified and the peptides were found to have specific activities defined by relative magnitude of response output rather than by uniqueness. A striking correlation between individual ZmPep-elicited changes in levels of jasmonic acid and ethylene and the magnitude of induced defense responses was observed, indicating that collectively ZmPeps may regulate immune output through rheostat-like tuning of phytohormone levels. Peptide structure-function studies and ligand-receptor modeling revealed structural features critical to ZmPep function and led to identification of ZmPep5a as a potential antagonist peptide able to competitively inhibit activity of other ZmPeps, a regulatory mechanism not previously observed for this family.</div>
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Data generation: Sat Nov 21 12:33:18 2020. Site generation: Sat Nov 21 12:33:47 2020