Biotechnology Bulletin ›› 2026, Vol. 42 ›› Issue (7): 214-225.doi: 10.13560/j.cnki.biotech.bull.1985.2025-0889

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Genome-wide Identification and Expression Analysis of MYC Transcription Factors in Cinnamomum camphora

XIN Qing1,2, ZHENG Yong-jie2, LI Yu-hua2, TU Bai-lian2, LIU Xin-liang2, ZHANG Yue-ting2, WU Yan-fang1,2()   

  1. 1.College of Forestry, Jiangxi Agricultural University, Nanchang 330045
    2.Jiangxi Academy of Forestry, Nanchang 330013
  • Received:2025-08-18 Online:2026-07-26 Published:2026-07-20
  • Contact: WU Yan-fang E-mail:yanfangwu2012@163.com

Abstract:

Objective MYC transcription factors (TFs) are core regulators of the jasmonic acid (JA) signalling pathway and play crucial roles in modulating plant growth, development, and secondary metabolism. Identification and analysis of MYC TFs in Cinnamomum camphora will provide a theoretical basis for investigating the biosynthesis of terpenoids and other secondary metabolites, as well as plant growth and development. Method Bioinformatics approaches were employed to perform genome-wide identification of the CcMYC family, including chromosomal localization, physicochemical properties, subcellular localization, phylogenetic relationships, gene structure, promoter regions, and protein-protein interaction (PPI) networks. Combined with quantitative real-time PCR (RT-qPCR), the expression patterns of the CcMYC gene family in six chemotypes of C. camphora was analyzed. Result CcMYC1-CcMYC12 were unevenly distributed across the 10 chromosomes. Proteins encoded by the CcMYC family contained 629 amino acids, an average molecular mass of 69.64 kD, and theoretical isoelectric points ranging from 5.15 to 6.69; their secondary structures were mainly composed of α-helices and random coils. Subcellular localization prediction showed that CcMYC12 was predominantly localized in the nucleus. Phylogenetic analysis revealed that the CcMYC genes were clustered into three distinct groups. Interspecific collinearity analysis indicated that segmental duplication events occurred in the CcMYC gene family, and collinear orthologs of CcMYC1, CcMYC4 and CcMYC5 were identified in Arabidopsis thaliana, Oryza sativa and Populus trichocarpa, respectively. Analysis of cis-acting elements in the promoter regions suggested that the expressions of CcMYC genes may be induced by light, diverse plant hormones, as well as defense and stress stimuli. Protein-protein interaction (PPI) analysis further revealed that CcMYC3, CcMYC7, CcMYC8 and CcMYC11 may play vital roles in regulating the biosynthesis and accumulation of secondary metabolites including flavonoids and terpenoids in C. camphora. Conclusion A total of 12 MYC family members have been identified from the genome of C. camphora. Among them, CcMYC1 and CcMYC8 are highly expressed in the D-borneol chemotype and citral chemotype, while CcMYC11 and CcMYC12 exhibit high expressions in the linalool chemotype. These genes may contribute significantly to the biosynthesis and accumulation of essential oil main components, terpenoids and other secondary metabolites in different chemotypes of C. camphora.

Key words: Cinnamomum camphora, MYC transcription factor, secondary metabolism, bioinformatics analysis, genome-wide identification