Identification of MYB Gene Family in medicinal tea tree Melaleuca alternifolia (Maiden & Betche) Cheel and Analysis of Members Regulating Terpene Biosynthesis

Author:

Zhang Xiaoning1,Xu Zhanwu2,Liu Buming3,Xiao Yufei1,Chai Ling3,Zhong Lianxiang1,Huo Heqiang4,Liu Li2,Yang Hong2,Liu Hailong1

Affiliation:

1. Guangxi Foresrty Research Institute

2. Hubei University

3. Guangxi Institute of Chinese Medicine&Pharmaceutical Science

4. Mid-Florida Research and Education Center, Department of Environmental Horticulture

Abstract

Abstract Background The tea tree (Melaleuca alternifolia) is renowned for its production of tea tree oil (TTO), an essential oil primarily composed of terpenes extracted from its shoot. MYB transcription factors, which are one of the largest TF families, play a crucial role in regulating primary and secondary metabolite synthesis. However, knowledge of the MYB gene family in M. alternifolia is limited. Methods and results Here, we conducted a comprehensive genome-wide analysis of MYB genes in M. alternifolia, referred to as MaMYBs, including phylogenetic relationships, structures, promoter regions, and GO annotations. Our findings classified 219 MaMYBs into four subfamilies: one 5R-MYB, four 3R-MYBs, sixty-one MYB-related, and the remaining 153 are all 2R-MYBs. Seven genes (MYB189, MYB146, MYB44, MYB29, MYB175, MYB162, and MYB160) were linked to terpenoid synthesis based on GO annotation. Phylogenetic analysis with Arabidopsis homologous MYB genes suggested that MYB193 and MYB163 may also be involved in terpenoid synthesis. Additionally, through correlation analysis of gene expression and metabolite content, we identified 42 MYB genes associated with metabolite content. Conclusion The results provide valuable insights into the importance of MYB transcription factors in essential oil production in M. alternifolia. These findings lay the groundwork for a better understanding of the MYB regulatory network and the development of novel strategies to enhance essential oil synthesis in M. alternifolia.

Publisher

Research Square Platform LLC

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