Journal
HORTICULTURE RESEARCH
Volume 9, Issue -, Pages -Publisher
OXFORD UNIV PRESS INC
DOI: 10.1093/hr/uhac116
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Funding
- National Key Research and Development Program [2018YFD1000200]
- National Natural Science Foundation of China [32072635]
- Key Research and Development Program of Zhejiang Province [2021C02015]
- Fruit New Varieties Breeding Project of Zhejiang Province [2021C02066-8]
- Fok Ying Tung Education Foundation [161028]
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The study demonstrates that exogenous ASA treatment significantly reduces ethylene production and inhibits the activity of related enzymes in kiwifruit tissues. Transcriptome analysis and transcription factor screening reveal ASA-responsive regulators for ethylene biosynthetic genes. Additionally, abundantly expressed genes are found in both ASA-treated and control tissues. The findings suggest that ASA inhibits ethylene biosynthesis by regulating protein activity at a post-transcriptional level.
Levels of ethylene, implicated in the induction of fruit ripening in a diverse array of plants, are influenced by genetic and environmental factors, such as other plant hormones. Among these, salicylic acid (SA) and its derivative, acetylsalicylic acid (ASA), have been demonstrated to inhibit ethylene biosynthesis in fruit, yet the underlying regulatory mechanisms remain elusive. Here, we showed that treatment with exogenous ASA dramatically reduced ethylene production, as well as activities of ACC synthase (ACS) and ACC oxidase (ACO), in kiwifruit tissues. Comparative transcriptome analysis indicated the differential expression of ethylene biosynthetic genes (AdACS1/2 and AdACO5). A screen of transcription factors indicated that AdERF105L and AdWRKY29 were ASA-responsive regulators of AdACS1/2 and AdACO5, respectively. In addition to these genes, AdACS3 and AdACO3 were abundantly expressed in both ASA-treated and control tissues. AdACS3 protein was phosphorylated and stabilized by AdMPK16, a mitogen-activated protein kinase, while AdACO3 activity was enhanced by AdAP, an aspartic peptidase. Exogenous ASA downregulated AdMPK16 and AdAP, thereby influencing ethylene biosynthesis at a post-transcriptional level. These findings led us to propose a multidimensional system for inhibition of ethylene biosynthesis by ASA, inducing differential expression of some ethylene biosynthesis genes, as well as differential effects on protein activity on other targets.
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