Biotechnology Bulletin ›› 2026, Vol. 42 ›› Issue (11): 186-195.doi: 10.13560/j.cnki.biotech.bull.1985.2026-0356

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ApGA20ox1 Positively Regulates Flowering of Agapanthus praecox via the Gibberellin Metabolic Pathway

YUE Jian-hua1,2, FANG Ting-ting1, CHEN Guan-qun2, SHEN Xiao-hui2()   

  1. 1.School of Horticulture, Xinyang Agriculture and Forestry University, Xinyang 464100
    2.School of Design, Shanghai Jiao Tong University, Shanghai 200240
  • Received:2026-03-30 Online:2026-11-26 Published:2026-11-03
  • Contact: SHEN Xiao-hui E-mail:shenxh62@sjtu.edu.cn

Abstract:

Objective To elucidate the mechanism by which ApGA20ox1, a key gibberellin (GA) biosynthesis gene, regulates flowering in Agapanthus praecox, and to provide a theoretical basis for flowering regulation and genetic improvement in this species. Method Total RNA was extracted from leaves of A. praecox, and the full-length coding sequence of ApGA20ox1 was cloned using RACE (rapid amplification of cDNA ends). Sequence homology, subcellular localization, and prokaryotic expression were analyzed. The gene was heterologously overexpressed in Arabidopsis thaliana, whereas its endogenous expression was silenced in A. praecox via RNA interference (RNAi). Changes in GA contents and expression patterns of flowering-related genes were investigated through transcriptome sequencing and GA-targeted metabolomics. Result The ApGA20ox1 gene was successfully cloned from A. praecox. Its full-length ORF was 1 086 bp, encoding a protein of 361 amino acids, and the genomic sequence contained three exons and two introns. The gene was evolutionarily conserved, and its encoded protein was predicted to have a molecular weight of approximately 41.1 kD and to localize in the cytoplasm. Genetic transformation assays demonstrated that heterologous overexpression of ApGA20ox1 significantly advanced bolting time in A. thaliana. RNAi-mediated suppression of ApGA20ox1 expression significantly affected the expression of GA synthase genes and metabolic flux in A. praecox leaves. Among these genes, the expression levels of GA20ox6 and GA3ox1 were significantly upregulated, whereas those of GA20ox1, GA20ox3, GA20ox4, and GA2ox3 were markedly downregulated. The contents of GA4, GA24, GA9, GA44, GA19, and GA20 decreased significantly, whereas those of GA3, GA51, GA29, and GA34 increased remarkably. Among flowering-related genes, all members of the FLC and SOC1 families were significantly downregulated, whereas most members of the CO family were upregulated. Additionally, the expression of FT and LFY genes was significantly upregulated. Conclusion ApGA20ox1 was identified as a critical gene that regulates GA biosynthesis and positively regulates flowering through the GA pathway in A. praecox. RNAi-mediated silencing of ApGA20ox1 markedly repressed the expression of the flowering integrator gene SOC1 and blocked the flowering pathway.

Key words: Agapanthus praecox, ApGA20ox1, gibberellin, flowering regulation, SOC1, heterologous overexpression, targeted metabolomics, transcriptome