Melatonin is a multifunctional molecule that has been widely discovered in most plants. An increasing number of studies have shown that melatonin plays essential roles in plant growth and stress tolerance. It has been extensively applied to alleviate the harmful effects of abiotic stresses. In view of its role in regulating aspects of plant growth and development, we ponder and summarize the scientific discoveries about seed germination, root development, flowering, fruit maturation, and senescence. Under abiotic and biotic stresses, melatonin brings together many pathways to increase access to treatments for the symptoms of plants and to counteract the negative effects. It has the capacity to tackle regulation of the redox, plant hormone networks, and endogenous melatonin. Furthermore, the expression levels of several genes and the contents of diverse secondary metabolites, such as polyphenols, terpenoids, and alkaloids, were significantly altered. In this review, we intend to examine the actions of melatonin in plants from a broader perspective, explore the range of its physiological functions, and analyze the relationship between melatonin and other metabolites and metabolic pathways.

Anthocyanins produce different-colored pigments in plant organs, which provide ornamental value. Thus, this study was conducted to understand the mechanism of anthocyanin synthesis in ornamental plants. Phoebe bournei, a Chinese specialty tree, has high ornamental and economic value due to its rich leaf color and diverse metabolic products. Here, the metabolic data and gene expression of red P. bournei leaves at the three developmental stages were evaluated to elucidate the color-production mechanism in the red-leaved P. bournei species. First, metabolomic analysis identified 34 anthocyanin metabolites showing high levels of cyanidin-3-O-glucoside (cya-3-O-glu) in the S1 stage, which may suggest that it is a characteristic metabolite associated with the red coloration of the leaves. Second, transcriptome analysis showed that 94 structural genes were involved in anthocyanin biosynthesis, especially flavanone 3′-hydroxy-lase (PbF3′H), and were significantly correlated with the cya-3-O-glu level. Third, K-means clustering analysis and phylogenetic analyses identified PbbHLH1 and PbbHLH2, which shared the same expression pattern as most structural genes, indicating that these two PbbHLH genes may be regulators of anthocyanin biosynthesis in P. bournei. Finally, overexpression of PbbHLH1 and PbbHLH2 in Nicotiana tabacum leaves triggered anthocyanin accumulation. These findings provide a basis for cultivating P. bournei varieties that have high ornamental value.

WUSCHEL-related homeobox (WOX) transcription factor (TF)-encoding genes play crucial roles during embryo development. The function of WOX genes in embryonic development has been thoroughly studied in Arabidopsis thaliana, but little is known about their function in woody species, especially Phoebe bournei, an endemic and endangered species in China. In the present study, a total of 15 WOX genes were identified in P. bournei, and phylogenetic analysis resulted in their assignment to three typical clades: an ancient clade, an intermediate clade, and a modern/WUS clade. The gene structure and sequence characteristics and the physicochemical properties of WOX proteins were also analyzed. Promoter prediction indicated that WOX genes are likely involved in plant growth and development and hormone responses. Subsequently, we evaluated the expression patterns of WOX genes in response to auxin (IAA), abscisic acid (ABA), and methyl jasmonate (MeJA) treatments. According to tissue-specific expression patterns, we screened nine WOX genes that were present in embryonic calli and that might participate in the somatic embryogenesis (SE) of P. bournei. Furthermore, the expression profiles of these nine WOX genes during three phases of embryogenic calli development and three phases of somatic embryo development, namely, spheroid embryogenesis, immature cotyledon-producing embryogenesis and mature cotyledon-producing embryogenesis, were monitored. Overall, we systematically analyzed the expression patterns of WOX genes in P. bournei during SE, the information of which provides a basis for further elucidating the molecular mechanism through which WOX TFs function in P. bournei embryo development.