Cao Zihang, Wang Jianzhao, Gong Yikai, Yin Xian, Yang Cheng, Yang Ting, Wu Tian
Engineering Technology Research Center of National Forestry and Grassland Administration on Southwest Landscape Architecture, Yunnan Province Engineering Research Center for Functional Flower Resources and Industrialization, College of Landscape and Horticulture, Southwest Forestry University, Kunming, China.
Front Plant Sci. 2025 Aug 15;16:1641401. doi: 10.3389/fpls.2025.1641401. eCollection 2025.
holds cultural and horticultural significance in traditional Chinese gardens, as a regional endemic species in Yunnan Province. However, during the regeneration process of , there is often a phenomenon of low efficiency of adventitious bud differentiation or no adventitious bud differentiation at all.
In previous study, we observed significant morphological differences between the callus tissues of 'Zipao' and wild species. The callus of 'Zipao' was white and loosely textured, the wild species was green and hard. To investigate the differences between these two types of callus, we conducted transcriptome analysis and identified a differentially expressed gene , which is closely related to the synthesis of glutathione (GSH). Heterologous transformation of into tobacco () was conducted.
The gene promoted the synthesis of endogenous auxin and cytokinin in transgenic tobacco by regulating the expression of transcription factors related to auxin and cytokinin. Exogenous IBA, 6-BA, and red-blue light treatment increased the levels of auxins and cytokinins in callus, thereby promoting adventitious bud differentiation. Additionally, interacted with and genes, facilitating GSH and AsA synthesis and clearing ROS.
在传统中国园林中具有文化和园艺意义,是云南省的一种区域特有物种。然而,在其再生过程中,常常存在不定芽分化效率低或根本没有不定芽分化的现象。
在先前的研究中,我们观察到‘紫袍’的愈伤组织与野生种之间存在显著的形态差异。‘紫袍’的愈伤组织为白色且质地疏松,野生种为绿色且坚硬。为了研究这两种愈伤组织之间的差异,我们进行了转录组分析,并鉴定出一个差异表达基因,其与谷胱甘肽(GSH)的合成密切相关。将该基因异源转化到烟草(Nicotiana tabacum)中。
该基因通过调节与生长素和细胞分裂素相关的转录因子的表达,促进转基因烟草中内源生长素和细胞分裂素的合成。外源吲哚丁酸(IBA)、6-苄氨基腺嘌呤(6-BA)和红蓝光照处理提高了愈伤组织中生长素和细胞分裂素的水平,从而促进不定芽分化。此外,该基因与GR和MDHAR基因相互作用,促进谷胱甘肽和抗坏血酸(AsA)的合成并清除活性氧(ROS)。