Zhang Haiqi, Cheng Jingjing, Wang Xue, Dai Pingyuan, Zhang Hongjuan, Zhou Fengli, Yang Chengquan, Zhai Rui, Wang Zhigang, Xu Lingfei
College of Horticulture, Northwest A&F University, Taicheng Road No. 3, Yangling, Shaanxi Province, 712100 China.
Key Laboratory of Horticultural Crop Germplasm Innovation and Utilization (Co-construction by Ministry and Province), Institute of Horticulture, Anhui Academy of Agricultural Sciences, Nongke South Road No. 40, Luyang District, Hefei, Anhui Province, 230001 China.
Hortic Res. 2025 Jan 21;12(5):uhaf021. doi: 10.1093/hr/uhaf021. eCollection 2025 May.
Parthenocarpy can ensure fruit setting without fertilization and generate seedless fruits. has been shown to play a role in gibberellin (GA)-induced parthenocarpy in pears. However, the transcriptional response mechanism of to GA remains unclear. In this study, using a yeast one-hybrid assay combined with co-expression analysis, was initially identified as a transcription regulator of , which was further confirmed by electrophoretic mobility shift assay (EMSA) and dual-luciferase reporter assays. The biofunction of was further verified using transient transgene tests, stable transgenic pear callus and tomato. overexpression resulted in reduced cell death and higher fluorescence intensity after fluoresce diacetate (FDA) staining, as well as delayed fruit-drop by increasing expression in unpollinated pear fruitlets and callus. In contrast, silencing caused cell death and early fruit-drop with decreased expression. Moreover, after emasculation, heterologous overexpression of induced parthenocarpy and enlarged seed size in pollinated tomato fruits. Silencing , a homolog of in tomatoes, resulted in smaller fruit and seed size, and these traits were restored by co-overexpression with . Furthermore, we investigated the protein interaction between PbMYB56 and PbDELLA, which is crucial component of the GA signaling pathway. This interaction inhibited PbMYB56-induced transcriptional activation of . Co-overexpression of and contributed to reduced seed development and loss of parthenocarpy potential in tomatoes. Collectively, our study identifies PbDELLA-PbMYB56- as a regulatory module of GA-induced pseudo-embryo and parthenocarpy development, offering insights into the mechanism underlying parthenocarpy formation in pears.
单性结实可确保在不施肥的情况下坐果并产生无籽果实。已证明其在梨的赤霉素(GA)诱导的单性结实中起作用。然而,其对GA的转录反应机制仍不清楚。在本研究中,通过酵母单杂交试验结合共表达分析,最初鉴定为的转录调节因子,通过电泳迁移率变动分析(EMSA)和双荧光素酶报告基因试验进一步证实。通过瞬时转基因试验、稳定转基因梨愈伤组织和番茄进一步验证了的生物学功能。过表达导致细胞死亡减少,荧光素二乙酸酯(FDA)染色后荧光强度更高,并且通过增加未授粉梨幼果和愈伤组织中的表达延迟落果。相反,沉默导致细胞死亡和早期落果,表达降低。此外,去雄后,在授粉番茄果实中异源过表达诱导单性结实并增大种子大小。沉默番茄中的同源物,导致果实和种子变小,并且通过与共过表达恢复了这些性状。此外,我们研究了PbMYB56和PbDELLA之间的蛋白质相互作用,PbDELLA是GA信号通路的关键组成部分。这种相互作用抑制了PbMYB56诱导的转录激活。和共过表达导致番茄种子发育减少和单性结实潜力丧失。总体而言,我们的研究确定PbDELLA - PbMYB56 - 为GA诱导的假胚和单性结实发育的调节模块,为梨中单性结实形成的机制提供了见解。