Uridine diphosphate glycosyltransferases (UDP-GTs, UGTs), which are regulated by UGT genes, play a crucial role in glycosylation. In vivo, the activity of UGT genes can affect the availability of metabolites and the rate at which they can be eliminated from the body. UGT genes can exert their regulatory effects through mechanisms such as post-transcriptional modification, substrate subtype specificity, and drug interactions. Phoebe bournei is an economically significant tree species that is endemic to southern China. Despite extensive studies on the UGT gene family in various species, a comprehensive investigation of the UGT family in P. bournei has not been reported. Therefore, we conducted a systematic analysis to identify 156 UGT genes within the entire P. bournei genome, all of which contained the PSPG box. The PbUGT family consists of 14 subfamilies, consistent with Arabidopsis thaliana. We observed varying expression levels of PbUGT genes across different tissues in P. bournei, with the following average expression hierarchy: leaf > stem xylem > stem bark > root xylem > root bark. Covariance analysis revealed stronger covariance between P. bournei and closely related species. In addition, we stressed the seedlings with 10% NaCl and 10% PEG-6000. The PbUGT genes exhibited differential expression under drought and salt stresses, with specific expression patterns observed under each stress condition. Our findings shed light on the transcriptional response of PbUGT factors to drought and salt stresses, thereby establishing a foundation for future investigations into the role of PbUGT transcription factors.

The TCP gene family encodes plant transcription factors crucial for regulating growth and development. While TCP genes have been identified in various species, they have not been studied in Phoebe bournei (Hemsl.). This study identified 29 TCP genes in the P. bournei genome, categorizing them into Class I (PCF) and Class II (CYC/TB1 and CIN). We conducted analyses on the PbTCP gene at both the protein level (physicochemical properties) and the gene sequence level (subcellular localization, chromosomal distribution, phylogenetic relationships, conserved motifs, and gene structure). Most P. bournei TCP genes are localized in the nucleus, except PbTCP9 in the mitochondria and PbTCP8 in both the chloroplast and nucleus. Chromosomal mapping showed 29 TCP genes unevenly distributed across 10 chromosomes, except chromosome 8 and 9. We also analyzed the promoter cis-regulatory elements, which are mainly involved in plant growth and development and hormone responses. Notably, most PbTCP transcription factors respond highly to light. Further analysis revealed three subfamily genes expressed in five P. bournei tissues: leaves, root bark, root xylem, stem xylem, and stem bark, with predominant PCF genes. Using qRT-PCR, we examined six representative genes—PbTCP16, PbTCP23, PbTCP7, PbTCP29, PbTCP14, and PbTCP15—under stress conditions such as high temperature, drought, light exposure, and dark. PbTCP14 and PbTCP15 showed significantly higher expression under heat, drought, light and dark stress. We hypothesize that TCP transcription factors play a key role in growth under varying light conditions, possibly mediated by auxin hormones. This work provides insights into the TCP gene family’s functional characteristics and stress resistance regulation in P. bournei.

Grafting is a common technique used to enhance watermelon yield under biotic and abiotic stress conditions; however, it may influence fruit development and quality. This study evaluated the impact of grafting on the fruit quality attributes and volatile profiles of 'Ningnongke huadai' watermelon using 11 commercial rootstocks, encompassing wild watermelons, bottle gourds, and pumpkins. Significant variations were observed in fruit weight, length, rind thickness, firmness of rind and flesh, and central soluble solids content. Notably, wild watermelon grafting increased central soluble solids, while pumpkin-grafted fruits exhibited higher fruit weight but lower central soluble solids. The analysis identified 122 volatile compounds in watermelon samples, primarily ketones, aldehydes, and alcohols. Regarding volatile composition, bottle gourd and wild watermelon grafts did not significantly differ from non-grafted watermelons, whereas pumpkin-grafted fruits showed distinctive volatile profiles characterized by higher aldehyde content and lower levels of alcohols and aromatic hydrocarbons. In conclusion, wild watermelon rootstocks increased soluble solids and had minimal impact on the volatile profiles of grafted fruits, making them potentially suitable for commercial production of 'Ningnongke huadai' watermelon. The evident variability in volatile profiles among grafting combinations underscores the need for watermelon rootstock breeding programs to account for the influence of rootstocks on fruit aroma.

The BRI1-EMS-SUPPRESSOR 1 (BES1) family comprises plant-specific transcription factors, which are distinguished by atypical bHLH domains. Over the past two decades, genetic and biochemical studies have established that members of the BRI1-EMS-SUPPRESSOR 1 (BES1) family are crucial for regulating the expression of genes involved in brassinosteroid (BR) response in rapeseed. Due to the significance of the BES1 gene family, extensive research has been conducted to investigate its functional properties. This study presents a comprehensive identification and computational analysis of BES1 genes in ‘Tieguanyin’ (TGY) tea (Camellia sinensis). A total of 10 BES1 genes were initially identified in the TGY genome. Through phylogenetic tree analysis, this study uniquely revealed that CsBES1.2 and CsBES1.5 cluster with SlBES1.8 from Solanum lycopersicum, indicating their critical roles in fruit growth and development. Synteny analysis identified 20 syntenic genes, suggesting the conservation of their evolutionary functions. Analysis of the promoter regions revealed two types of light-responsive cis-elements, with CsBES1.4 exhibiting the highest number of light-related cis-elements (13), followed by CsBES1.9 and CsBES1.10. Additional validation via qRT-PCR experiments showed that CsBES1.9 and CsBES1.10 were significantly upregulated under light exposure, with CsBES1.10 reaching approximately six times the expression level of the control after 4 h. These results suggest that CsBES1.9 and CsBES1.4 could play crucial roles in responding to abiotic stress. This study offers novel insights into the functional roles of the BES1 gene family in ‘Tieguanyin’ tea and establishes a significant foundation for future research, especially in exploring the roles of these genes in response to abiotic stresses, such as light exposure.

PIN-formed (PIN) proteins—specific transcription factors that are widely distributed in plants—play a pivotal role in regulating polar auxin transport, thus influencing plant growth, development, and abiotic stress responses. Although the identification and functional validation of PIN genes have been extensively explored in various plant species, their understanding in woody plants—particularly the endangered species Phoebe bournei (Hemsl.) Yang—remains limited. P. bournei is an economically significant tree species that is endemic to southern China. For this study, we employed bioinformatics approaches to screen and identify 13 members of the PIN gene family in P. bournei. Through a phylogenetic analysis, we classified these genes into five sub-families: A, B, C, D, and E. Furthermore, we conducted a comprehensive analysis of the physicochemical properties, three-dimensional structures, conserved motifs, and gene structures of the PbPIN proteins. Our results demonstrate that all PbPIN genes consist of exons and introns, albeit with variations in their number and length, highlighting the conservation and evolutionary changes in PbPIN genes. The results of our collinearity analysis indicate that the expansion of the PbPIN gene family primarily occurred through segmental duplication. Additionally, by predicting cis-acting elements in their promoters, we inferred the potential involvement of PbPIN genes in plant hormone and abiotic stress responses. To investigate their expression patterns, we conducted a comprehensive expression profiling of PbPIN genes in different tissues. Notably, we observed differential expression levels of PbPINs across the various tissues. Moreover, we examined the expression profiles of five representative PbPIN genes under abiotic stress conditions, including heat, cold, salt, and drought stress. These experiments preliminarily verified their responsiveness and functional roles in mediating responses to abiotic stress. In summary, this study systematically analyzes the expression patterns of PIN genes and their response to abiotic stresses in P. bournei using whole-genome data. Our findings provide novel insights and valuable information for stress tolerance regulation in P. bournei. Moreover, the study offers significant contributions towards unraveling the functional characteristics of the PIN gene family.