Camellia’s ornamental value is constrained by its natural winter–spring flowering period. Although the discovery of Camellia azalea provides important germplasm resources for developing cultivars with year-round flowering, the molecular mechanisms underlying flowering time variation remain unclear. Here, we investigated three germplasms with distinct flowering patterns: winter–spring flowering Camellia japonica ‘Tieke Baozhu’, summer–autumn flowering Camellia azalea, and their hybrid Camellia ‘Lingnan Yuanbao’ inheriting the latter’s flowering traits. Integrated transcriptomic and metabolomic analyses revealed that differentially expressed genes (DEGs) and metabolites (DAMs) were mainly enriched in the pathways related to photoperiod regulation, plant hormone synthesis and signal transduction and flavonoid synthesis. The transcription factor (TF) analysis revealed that the bHLH and MYB TF families were significantly differentially expressed in different Camellia germplasm, suggesting their potential involvement in the regulation of flowering time through the plant hormone signal transduction and photoperiod pathway. Meanwhile, photoperiod regulation related genes, including Cryptochrome circadian regulator (CRY), Timing of CAB expression 1 (TOC1), and phytochrome interacting factor 3 (PIF3), showed significant expression differences, further confirming the photoperiod pathway’s crucial regulatory function. In terms of plant hormone levels, there were significant differences in the levels of gibberellin (GA), abscisic acid (ABA), and jasmonic acid (JA) among Camellia germplasm. The differential expression characteristics of DELLA (Asp-Glu-Leu-Leu-Ala) proteins indicated that the GA signal transduction pathway was one of the key factors regulating flowering time in Camellia. Additionally, metabolomics analyses showed significant differences in flavonoid metabolite content among Camellia germplasm, which was significantly correlated with the different developmental stages of the buds. Our findings provide a theoretical basis for the molecular breeding of everblooming Camellia cultivars, advancing the understanding of flowering regulation mechanism in ornamental species.

Ficus virens is a deciduous tree that is highly valuable both economically and medicinally. Like other plants with ‘red young leaves’, the red-leaf period of most F. virens trees lasts only a few days, and the red leaves have little ornamental value. However, in recent years, some lines of F. virens with bright red young leaves and a prolonged red-leaf period have been utilized for urban greening. To explore the mechanism of the different lengths of the duration of F. virens leaves, we analyzed the physiology and changes in gene expression during the development of two varieties of leaves. The detection of anthocyanin in different developmental stages of the F. virens leaves showed that the changes in color of the red leaves of F. virens were primarily caused by the change in anthocyanin content. A transcriptome analysis showed that the expression of genes related to the biosynthesis of anthocyanin changed significantly during the development of leaves. A MYB gene FvPAP1, which was consistent with the change in anthocyanin content, was identified. A real-time quantitative reverse transcription PCR analysis and heterologous expression transgenic studies showed that FvPAP1 promoted the biosynthesis of anthocyanins. The difference in the expression of FvPAP1 in time and intensity in the young leaves may be the reason for the difference in the duration of the red-leaf period in different lines of F. virens. A sequence analysis showed that the cDNA sequence of FvPAP1 was polymorphic, and possible reasons were discussed. These results can provide insight for similar studies on the mechanism of the formation of red coloring in other woody plant leaves and provide molecular targets to breed new materials with more prolonged red-leaf periods in F. virens.

Carex is a type of herbaceous plant with high application value, playing an important role in the urban periphery. Due to its unique morphology and ecological characteristics, Carex is widely used in various fields, such as landscaping, ecological restoration and soil and water conservation, which help to maintain the balance of the ecosystem. In order to explore the potential molecular mechanisms of shade tolerance in Carex, transcriptome and metabolome sequencing were performed on the leaves of the shade = tolerant species Carex adrienii E. G. Camus. under 80% shade and no shade conditions. Compared to control group (CK), the total chlorophyll, chlorophyll a, chlorophyll b and total carotenoid content in the C. adrienii leaves of the shading treatment were significantly upregulated. The antioxidant enzyme activity of the leaves, including superoxide dismutase (SOD), peroxidase (POD), and catalase (CAT), were also remarkably upregulated in the shading treatment groups. In addition, the net photosynthesis rate (Pn), stomatal conductance (Gs) and transpiration rate (Tr) of the leaves were reduced, and the intercellular CO₂ concentration (Ci) of the leaves was increased under shade. The transcriptome identified 5056 differentially expressed genes (DEGs) and the metabolome identified 889 differential accumulated metabolites (DAMs) in three treated samples. The integrated transcriptomic and metabolomic analyses results showed that the DEGs and DAMs were enriched in photosynthesis, plant hormone signal transduction and flavonoid biosynthesis synthesis pathways. The ABA content of the C. adrienii leaves was significantly increased under shade. Therefore, the shading conditions led to changes in chlorophyll and abscisic acid (ABA), as well as the accumulation of flavonoids in C. adrienii, both of which were achieved by regulating genes involved in photosynthesis, plant hormone signal transduction and flavonoid biosynthesis molecular networks. Our results provide new knowledge for the molecular response and metabolic regulatory mechanisms of C. adrienii to shade stress, and valuable genetic resources for C. adrienii shade tolerance molecular breeding.