Xue Yuwei, Li Kexuan, Feng Wenli, Lai Zhongxiong, Liu Shengcai
Institute of Horticultural Biotechnology, Fujian Agriculture and Forestry University, Fuzhou 350002, China.
Key Laboratory of Ministry of Education for Genetics, Breeding and Multiple Utilization of Crops, Fujian Agriculture and Forestry University, Fuzhou 350002, China.
Plants (Basel). 2025 Jan 22;14(3):324. doi: 10.3390/plants14030324.
MYB (myeloblastosis) is one of the most abundant transcription factors in plants which regulates various biological processes. The molecular characteristics and function of R2R3-MYB transcription factors in amaranth remain unclear. In this study, 73 R2R3-MYB members were identified from the amaranth genome database and we further analyzed their chromosome position, conserved motifs, physiological and biochemical features, collinearity relationships, gene structure, phylogeny and -acting element. Based on the phylogenetic and expression pattern analysis, 14 candidate genes might be involved in the betalain synthesis. Amongst the 14 candidate genes, the expression level of was higher in 'Suxian No.1' than 'Suxian No.2', and also higher in the red section than in the green section of the same leaf in . The overexpression vector pCambia1301--GUS and VIGS (virus-induced gene silencing) vector pTRV2- were transferred into leaves of 'Suxian No.1' via an -mediated method. The results showed that overexpression could promote betalain synthesis. A yeast one-hybrid assay and dual luciferase reporter gene assay demonstrated that could bind to the promoter to promote betalain synthesis. These results indicated that promoted betalain biosynthesis in amaranth by activating the transcription. Our results could provide new insights into the betalain biosynthesis in amaranth.
MYB(成髓细胞瘤)是植物中最丰富的转录因子之一,它调控着各种生物学过程。苋菜中R2R3-MYB转录因子的分子特征和功能仍不清楚。在本研究中,从苋菜基因组数据库中鉴定出73个R2R3-MYB成员,并进一步分析了它们的染色体位置、保守基序、生理生化特征、共线性关系、基因结构、系统发育和作用元件。基于系统发育和表达模式分析,14个候选基因可能参与甜菜红素的合成。在这14个候选基因中,在‘宿苋1号’中的表达水平高于‘宿苋2号’,并且在同一叶片的红色部分也高于绿色部分。通过农杆菌介导的方法将过表达载体pCambia1301--GUS和病毒诱导基因沉默(VIGS)载体pTRV2-转入‘宿苋1号’叶片。结果表明,过表达可促进甜菜红素的合成。酵母单杂交试验和双荧光素酶报告基因试验表明,可与启动子结合以促进甜菜红素的合成。这些结果表明,通过激活转录促进了苋菜中甜菜红素的生物合成。我们的结果可为苋菜中甜菜红素的生物合成提供新的见解。