Palinuer Aiwaili

Chrysanthemum morifolium is an important ornamental crop whose flowering is strictly regulated by photoperiod. However, the molecular mechanisms linking photoperiod signals to floral meristem identity and organ development in Asteraceae remain unclear. In this study, we identified and characterized CmAFL1, a FUL-like MADS-box gene specific to the Asteraceae family, in the short-day cultivar ‘Jinba’. CmAFL1 expression is upregulated under short-day conditions, primarily expressed in the shoot apical meristem during flower bud differentiation and predominantly in the receptacle during organ development. RNA interference-mediated silencing of CmAFL1 resulted in delayed flowering, arrested inflorescence development, malformed tubular florets, plant dwarfism, and excessive lateral branching, indicating its pleiotropic roles in flowering time, plant architecture, and floral organ patterning. At the molecular level, yeast one-hybrid assays revealed that the photoperiod pathway transcription factor CmCOL4 directly binds to the promoter region of CmAFL1. Furthermore, yeast one-hybrid and dual-luciferase assays confirmed that CmAFL1 directly interacts with and activates the promoter of the E-class floral organ identity gene CmSEP3. Together, our findings identify a novel transcriptional regulatory module CmCOL4-CmAFL1-CmSEP3 that potentially links photoperiod signaling to floral meristem identity and organ specification in Chrysanthemums. While further in planta validation is warranted, these findings provide novel insights into photoperiodic flowering regulation in Asteraceae and may serve as a theoretical foundation for molecular breeding strategies targeting flowering time manipulation in ornamental Chrysanthemums.

Gibberellins (GAs) are key endogenous hormones regulating chrysanthemum flowering, and Gibberellin INSENSITIVE DWARF1 (GID1) is the core receptor of the gibberellin (GA) signaling pathway. However, the functional mechanism of CmGID1A remains unelucidated. Here, we constructed CmGID1A-RNAi silencing lines and characterized the biological function of CmGID1A by phenotypic identification, protein interaction assays, qRT-PCR and RNA-seq. The results of RT-qPCR showed that CmGID1A responds to short days and gibberellins. Inhibition of the expression of CmGID1A can significantly promote the transition of chrysanthemum from the vegetative growth stage to the reproductive growth stage and accelerate its flowering process. Bimolecular fluorescence complementation (BiFC) and yeast two-hybrid (Y2H) assays confirmed that CmGID1A interacts with the DELLA protein CmRGL1 in a gibberellin-dependent manner. RNA-seq results revealed that silencing of CmGID1A leads to a significant up-regulation of downstream Ethylene Response Factor 6 (ERF6) expression. Collectively, CmGID1A acts as a GA receptor to mediate GA signal transduction via interacting with CmRGL1, and regulates the expression of CmERF6 and other downstream genes, thereby participating in the regulation of floral transition in chrysanthemum. This study clarifies the core role of CmGID1A in the GA signaling pathway and provides novel experimental data for enriching the molecular regulatory mechanism of GA in floral transition in chrysanthemum.

Gibberellins (GAs) is a key endogenous hormone regulating chrysanthemum flowering, and Gibberellin INSENSITIVE DWARF1 (GID1) is the core receptor of the gibberellin (GA) signaling pathway. However, the functional mechanism of CmGID1A remains unelucidated. Here, we constructed CmGID1A-RNAi silencing lines, and characterized the biological function of CmGID1A by phenotypic identification, protein interaction assays, qRT-PCR and RNA-seq. The results of RT-qPCR showed that CmGID1A responds to short days and gibberellins. Inhibition of the expression of CmGID1A can significantly promote the transition of chrysanthemum from the vegetative growth stage to the reproductive growth stage and accelerate its flowering process. Bimolecular fluorescence complementation (BiFC) and yeast two-hybrid (Y2H) assays confirmed that CmGID1A interacts with the DELLA protein CmRGL1 in a gibberellin-dependent manner. RNA-seq results revealed that silencing of CmGID1A leads to a significant up-regulation of downstream Ethylene Response Factor 6 (ERF6) expression. Collectively, CmGID1A acts as a GA receptor to mediate GA signal transduction via interacting with CmRGL1, and regulates the expression of CmERF6 and other downstream genes, thereby participating in the regulation of floral transition in chrysanthemum. This study clarifies the core role of CmGID1A in the GA signaling pathway and provides novel experimental data for enriching the molecular regulatory mechanism of GA in floral transition in chrysanthemum.

[Background] Marigold (Tagetes erecta L.) is the main source of the natural pigment lutein. [Methods] In this study, Marigold served as the experimental material for systematic observation of floral organ development. Based on floral morphology and lutein content, the full-flowering stage was identified as the optimal harvesting period. [Results] Under different light intensity gradients (30–1500 μmol·m⁻²·s⁻¹), the highest lutein content in petals occurred at ≈500 μmol·m⁻²·s⁻¹. Increased light intensities promoted flowering and enlarged flower diameter while significantly shortening the growth cycle. Transcriptome analysis revealed that light intensity variation markedly influenced the expression of genes related to metabolic pathways, plant hormone signal transduction, and carotenoid biosynthesis, and enriched transcription factor families including bHLH, MYB, NAC, and WRKY. Metabolomic profiling identified lutein esters, such as lutein dimyristate and lutein dipalmitate, as the dominant accumulated forms, with their contents positively correlated with light intensity; under high light, intermediate metabolites, including α-cryptoxanthin and zeaxanthin, were significantly up-regulated. [Conclusions] This study clarifies the molecular mechanism by which light intensity precisely regulates lutein accumulation through coordinated synthesis, esterification, and degradation pathways, offering a theoretical foundation for light-regulated cultivation of T. erecta L. and efficient lutein production.