The MYB transcription factor SmMYB113 directly regulates ethylene-dependent flower abscission in eggplant

脱落 MYB公司 转录因子 乙烯利 双分子荧光互补 乙烯 生物 互补 植物 WRKY蛋白质结构域 荧光素酶 植物生理学 成熟 细胞生物学 拟南芥 突变体 酵母 基因 生物化学 转染 催化作用
作者
Jing Chen,Shenghui Jiang,Guobin Yang,Lu‐Jun Li,Jing Li,Fengjuan Yang
出处
期刊:Plant Physiology and Biochemistry [Elsevier BV]
卷期号:209: 108544-108544 被引量:1
标识
DOI:10.1016/j.plaphy.2024.108544
摘要

Flower abscission is an important developmental process that can significantly reduce the yield of horticultural plants. We previously reported that SmMYB113 is a key transcription factor promoting anthocyanin biosynthesis and improve fruit quality. However, the overexpression of SmMYB113 in eggplant increased flower drop rate and reduced fruit yield. Here, we elucidate the regulatory mechanisms of SmMYB113 on flower abscission in eggplant. RNA-seq analysis indicated that the regulation of flower abscission by SmMYB113 was associated with altered expression of genes related to ethylene biosynthesis and signal transduction, including ethylene biosynthetic genes SmACS1, SmACS8 and SmACO4. Then, the ethylene content in flowers and the function of ethephon (ETH, which promotes fruit ripening) and 1-Methylcyclopropene (1-MCP, which acts as an ethylene perception inhibitor) were analyzed, which revealed that SmMYB113 directly regulates ethylene-dependent flower abscission. Yeast one-hybrid and dual-luciferase assays revealed that SmMYB113 could directly bind to the promoters of SmACS1, SmACS8, and SmACO4 to activate their expression. Through construction of a yeast two-hybrid (Y2H) screening library, the protein SmERF38 was found to interact with SmMYB113, and verified by Y2H, bimolecular fluorescence complementation (BiFC), and luciferase complementation assay. Furthermore, dual-luciferase assays showed that SmERF38 enhanced the role of SmMYB113 on the promoters of SmACS1. Our results provided new insight into the molecular mechanism of flower abscission in eggplant.

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