Cinnamomum bodinieri is a tree species highly valued for its superior-quality timber and ecological benefits. However, its large-scale propagation is hindered by the low efficiency of adventitious root (AR) formation. This study investigated the physiological and molecular mechanisms underlying AR formation in C. bodinieri. The results revealed that ARs originate from callus tissue, with the root primordium classified as a latent type. During AR formation, concentrations of soluble protein and soluble sugar decreased, while the activities of superoxide dismutase (SOD), peroxidase (POD), and indole-3-acetic acid oxidase (IAAO) peaked 20 days after cutting (CB2), with polyphenol oxidase (PPO) activity exhibiting an “N”-shaped trend. These findings indicate that substantial nutrient consumption is required for AR formation, with SOD, POD, PPO, and IAAO positively regulating the process. Indole-3-acetic acid (IAA) levels significantly decreased during the early stages of cutting but increased thereafter, whereas the concentration of abscisic acid (ABA) continuously rose. Similar trends were observed for zeatin riboside (ZR) and gibberellic acid (GA). Transcriptome analysis identified 28 key genes involved in plant hormone signal transduction pathways. Furthermore, weighted gene co-expression network analysis (WGCNA) pinpointed 14 hub genes, including CYP94B3 and NAC82, linked to hormone-associated traits. Furthermore, quantitative real-time PCR (qRT-PCR) confirmed the accuracy of the transcriptome sequencing results. This analysis uncovered critical interactions between hormonal signaling pathways and pivotal gene networks. Overall, the findings highlight the central regulatory role of endogenous hormones in AR formation, with IAA serving as the predominant regulator.
Cinnamomum camphora is an ecologically and economically significant species, highly valued for its essential oil production and environmental benefits. Although a tissue culture system has been established for C. camphora, large-scale propagation remains limited due to the inconsistent formation of adventitious roots (ARs). This study investigated AR formation from callus tissue, focusing on associated physiological changes and gene expression dynamics. During AR induction, contents of soluble sugars and proteins decreased, alongside reduced activities of antioxidant enzymes, including superoxide dismutase (SOD), peroxidase (POD), and polyphenol oxidase (PPO). Levels of indole-3-acetic acid (IAA) and abscisic acid (ABA) decreased significantly throughout AR formation. Zeatin riboside (ZR) levels initially declined and then rose, whereas gibberellic acid (GA) levels displayed the opposite trend. Comparative transcriptomic and temporal expression analyses identified differentially expressed genes (DEGs), which were grouped into four distinct expression patterns. KEGG pathway enrichment indicated that 67 DEGs are involved in plant hormone signaling pathways and that 38 DEGs are involved in the starch and sucrose metabolism pathway. Additionally, protein–protein interaction network (PPI) analysis revealed ten key regulatory genes, which are mainly involved in auxin, cytokinin, GA, ABA, and ethylene signaling pathways. The reliability of the transcriptome data was further validated by quantitative real-time PCR. Overall, this study provides new insights into the physiological and molecular mechanisms underlying AR formation in C. camphora and offers valuable guidance for optimizing tissue culture systems.
Phoebe bournei is an important economic tree species in China, its large-scale propagation is limited by the difficulty of adventitious root (AR) formation in cuttings. In this study, morphological, physiological, and transcriptomic analyses were conducted to investigate the process of AR formation in P. bournei. The results showed that ARs mainly originated from callus tissue. During AR formation, soluble sugar and soluble protein contents changed significantly. Malondialdehyde (MDA) and oxygen free radicals (OFRs) peaked at first sampling stage (PB0), while the activities of polyphenol oxidase (PPO) and indoleacetic acid oxidase (IAAO) exhibited similar patterns. Lignin content increased during callus induction stage, whereas phenolic content continuously declined throughout rooting. Endogenous hormone levels also changed markedly, and Orthogonal partial least squares discriminant analysis (OPLS-DA) analysis indicated that indole-3-acetic acid (IAA) and abscisic acid (ABA) played dominant roles in this process. KEGG enrichment analysis revealed significant enrichment of the phenylpropanoid biosynthesis pathway in all three comparison groups. A total of 48 differentially expressed genes (DEGs) were enriched in plant hormone signal transduction pathways, with 22 and 14 genes associated with IAA and ABA signaling, respectively. Weighted gene co-expression network analysis (WGCNA) further identified two hub modules related to IAA and ABA contents, including eight hub genes such as D6PKL1 and ISTL1. Correlation analysis revealed that the hub genes D6PKL1 and HSP were significantly positively correlated with IAA4 in the IAA signaling pathway. Overall, this study provides new insights into the mechanisms underlying AR formation in P. bournei cuttings and offers a theoretical basis for optimizing its clonal propagation system.