Guan Yunxiao, Zhang Qiaoyu, Zhang Ting, Li Minghe, Ai Ye, Zhai Junwen, Lan Siren, Liu Zhong-Jian, Wu Shasha, Peng Donghui
Key Laboratory of National Forestry and Grassland Administration for Orchid Conservation and Utilization, College of Landscape Architecture and Art, Fujian Agriculture and Forestry University, Fuzhou, 350002, China.
The Innovation and Application Engineering Technology Research Center of Ornamental Plant Germplasm Resources in Fujian Province, Fuzhou, 350002, China.
BMC Plant Biol. 2025 May 24;25(1):696. doi: 10.1186/s12870-025-06713-5.
Phalaenopsis orchids, belonging to the Orchidaceae family, one of the largest groups of angiosperms, possess significant commercial value due to their fascinating flowers. Petal size is a vital trait that directly determines flower size and shape of Phalaenopsis. However, the genetic and developmental regulation of petal size in Phalaenopsis remains unexplored.
In this study, we tracked the petal growth pattern through five stages of flower opening, discovering that cell division stops at stage 2 and stages 3 to 5 are the critical periods of rapid petal expansion. RNA-seq was then conducted to further reveal the molecular mechanisms underlying petal size regulation. Gene ontology (GO) analysis indicated that the differentially expressed genes (DEGs) from the four comparable groups were both enriched in terms related to cell expansion. Endogenous hormone assays showed that auxin, cytokinin, and gibberellin were implicated in the petal growth of Phalaenopsis. Moreover, six auxin signaling pathway genes, 11 cell expansion-related genes, and 30 transcription factors (TFs) identified through trend analysis were abundantly expressed during the critical period of petal expansion, suggesting that they may influence petal size by regulating cell expansion. In contrast, 18 TFs exhibited the highest expression levels at the S1 stage, indicating their potential role in petal cell proliferation. Based on weighted gene co-expression network analysis (WGCNA), six hub genes (PaLOF2, PaSWEET11, PaVNI2, PaHDA3, PaPMEI3, PaXTH30) were screened from the green and yellow module which was highly associated with the petal size.
Our results lay a foundation for further exploration of the molecular mechanisms regulating petal size development and are significant for molecular breeding programs aimed at generating novel Phalaenopsis with desirable traits.
蝴蝶兰属于兰科植物,兰科是被子植物中最大的类群之一,因其迷人的花朵而具有重要的商业价值。花瓣大小是直接决定蝴蝶兰花朵大小和形状的关键性状。然而,蝴蝶兰花瓣大小的遗传和发育调控仍未得到探索。
在本研究中,我们通过花朵开放的五个阶段追踪了花瓣的生长模式,发现细胞分裂在第2阶段停止,第3至5阶段是花瓣快速扩展的关键时期。随后进行RNA测序以进一步揭示花瓣大小调控的分子机制。基因本体(GO)分析表明,来自四个可比组的差异表达基因(DEG)均在与细胞扩展相关的术语中富集。内源激素测定表明,生长素、细胞分裂素和赤霉素与蝴蝶兰花瓣生长有关。此外,通过趋势分析鉴定出的六个生长素信号通路基因、11个细胞扩展相关基因和30个转录因子(TF)在花瓣扩展的关键时期大量表达,表明它们可能通过调节细胞扩展来影响花瓣大小。相比之下,18个TF在S1阶段表现出最高表达水平,表明它们在花瓣细胞增殖中的潜在作用。基于加权基因共表达网络分析(WGCNA),从与花瓣大小高度相关的绿色和黄色模块中筛选出六个枢纽基因(PaLOF2、PaSWEET11、PaVNI2、PaHDA3、PaPMEI3、PaXTH30)。
我们的结果为进一步探索调节花瓣大小发育的分子机制奠定了基础,对于旨在培育具有理想性状的新型蝴蝶兰的分子育种计划具有重要意义。