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Involvement of CsWRKY70 in salicylic acid-induced citrus fruit resistance against Penicillium digitatum.

Identifieur interne : 000121 ( Main/Exploration ); précédent : 000120; suivant : 000122

Involvement of CsWRKY70 in salicylic acid-induced citrus fruit resistance against Penicillium digitatum.

Auteurs : Bing Deng [République populaire de Chine] ; Wenjun Wang [République populaire de Chine] ; Changqing Ruan [République populaire de Chine] ; Lili Deng [République populaire de Chine] ; Shixiang Yao [République populaire de Chine] ; Kaifang Zeng [République populaire de Chine]

Source :

RBID : pubmed:33082964

Abstract

Penicillium digitatum causes serious losses in postharvest citrus fruit. Exogenous salicylic acid (SA) can induce fruit resistance against various pathogens, but the mechanism remains unclear. Herein, a transcriptome-based approach was used to investigate the underlying mechanism of SA-induced citrus fruit resistance against P. digitatum. We found that CsWRKY70 and genes related to methyl salicylate (MeSA) biosynthesis (salicylate carboxymethyltransferase, SAMT) were induced by exogenous SA. Moreover, significant MeSA accumulation was detected in the SA-treated citrus fruit. The potential involvement of CsWRKY70 in regulating CsSAMT expression in citrus fruit was studied. Subcellular localization, dual luciferase, and electrophoretic mobility shift assays and an analysis of transient expression in fruit peel revealed that the nucleus-localized transcriptional activator CsWRKY70 can activate the CsSAMT promoter by recognizing the W-box element. Taken together, the findings from this study offer new insights into the transcriptional regulatory mechanism of exogenous SA-induced disease resistance in Citrus sinensis fruit.

DOI: 10.1038/s41438-020-00377-y
PubMed: 33082964
PubMed Central: PMC7527965


Affiliations:


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<i>Penicillium digitatum</i>
causes serious losses in postharvest citrus fruit. Exogenous salicylic acid (SA) can induce fruit resistance against various pathogens, but the mechanism remains unclear. Herein, a transcriptome-based approach was used to investigate the underlying mechanism of SA-induced citrus fruit resistance against
<i>P. digitatum</i>
. We found that
<i>CsWRKY70</i>
and genes related to methyl salicylate (MeSA) biosynthesis (salicylate carboxymethyltransferase, SAMT) were induced by exogenous SA. Moreover, significant MeSA accumulation was detected in the SA-treated citrus fruit. The potential involvement of CsWRKY70 in regulating
<i>CsSAMT</i>
expression in citrus fruit was studied. Subcellular localization, dual luciferase, and electrophoretic mobility shift assays and an analysis of transient expression in fruit peel revealed that the nucleus-localized transcriptional activator CsWRKY70 can activate the
<i>CsSAMT</i>
promoter by recognizing the W-box element. Taken together, the findings from this study offer new insights into the transcriptional regulatory mechanism of exogenous SA-induced disease resistance in
<i>Citrus sinensis</i>
fruit.</div>
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<i>Penicillium digitatum</i>
causes serious losses in postharvest citrus fruit. Exogenous salicylic acid (SA) can induce fruit resistance against various pathogens, but the mechanism remains unclear. Herein, a transcriptome-based approach was used to investigate the underlying mechanism of SA-induced citrus fruit resistance against
<i>P. digitatum</i>
. We found that
<i>CsWRKY70</i>
and genes related to methyl salicylate (MeSA) biosynthesis (salicylate carboxymethyltransferase, SAMT) were induced by exogenous SA. Moreover, significant MeSA accumulation was detected in the SA-treated citrus fruit. The potential involvement of CsWRKY70 in regulating
<i>CsSAMT</i>
expression in citrus fruit was studied. Subcellular localization, dual luciferase, and electrophoretic mobility shift assays and an analysis of transient expression in fruit peel revealed that the nucleus-localized transcriptional activator CsWRKY70 can activate the
<i>CsSAMT</i>
promoter by recognizing the W-box element. Taken together, the findings from this study offer new insights into the transcriptional regulatory mechanism of exogenous SA-induced disease resistance in
<i>Citrus sinensis</i>
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