ArticleFrontiers in plant science2022
Metabolome and transcriptome integration reveals insights into the process of delayed petal abscission in rose by STS.
Article in Frontiers in plant science, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.
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Who cites it
5 citing papers in PubMed, 10 citations in OpenAlex.
- Transcriptome based WGCNA analysis reveals the mechanisms underlying corolla abscission in blueberry (Vaccinium corymbosum L.).BMC plant biology · 2026Article
- Transcriptomic analysis reveals key genes and pathways involved in fruit abscission of Epimedium pubescens.BMC plant biology · 2025Article
- Abscission in plants: from mechanism to applications.Advanced biotechnology · 2024Review
- Reactive Oxygen and Related Regulatory Factors Involved in Ethylene-Induced Petal Abscission in Roses.Plants (Basel, Switzerland) · 2024Article
- Metabolite profiling and transcriptomic analyses demonstrate the effects of biocontrol agents on alkaloid accumulation in Fritillaria thunbergii.BMC plant biology · 2023Article
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Authors and funding
10 authors at 1 institution in 1 country.
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Abstract
The abscission of plant organs plays an important role in ensuring the normal life activities. Rose is one of the most important ornamental plants, and its premature abscission of petal has seriously affected the quality and commercial value. Silver Thiosulfate (STS) is an ethylene inhibitor, which is often used preservative to delay the senescence of fresh cut flowers. To understand the regulatory mechanism of petal abscission in rose by STS, integrative analysis of the metabolome and transcriptome profiles was performed in abscission zone (AZ) tissues of rose under different treatments (MOCK, STS, ETH, STS+ETH). The results showed that STS significantly delayed the petal abscission in phenotype and reduced the activity of two enzymes (pectinase and cellulase) associated with cell wall degradation in physiological level. STS affected the contents of five metabolites (shikonin, jasmonic acid, gluconolactone, stachyose and D-Erythrose 4-phosphate), and involved changes in the expression of 39 differentially expressed genes (DEGs) associated with these five metabolites. Five DEGs (
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