A genus-specific R2R3 MYB transcription factor, CsMYB34, regulates galloylated catechin biosynthesis in Camellia sinensis

Copyright © 2024 Elsevier Masson SAS. All rights reserved.

Bibliographische Detailangaben
Veröffentlicht in:Plant physiology and biochemistry : PPB. - 1991. - 219(2024) vom: 15. Dez., Seite 109401
1. Verfasser: Xu, Jianmei (VerfasserIn)
Weitere Verfasser: Li, Jingyi, Liu, Yihao, Zheng, Peng, Liu, Shaoqun, Sun, Binmei
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2024
Zugriff auf das übergeordnete Werk:Plant physiology and biochemistry : PPB
Schlagworte:Journal Article Camellia sinensis Flavonoid pathway Galloylated catechins MYB transcription factor Regulation
Beschreibung
Zusammenfassung:Copyright © 2024 Elsevier Masson SAS. All rights reserved.
Galloylated catechins are the dominant polyphenols in Camellia sinensis (L.) O. Kuntze. The mechanisms responsible for accumulation of these specialized metabolites in tea plants remains unclear. This paper presents an extended member of subgroup 5 of transcription factors R2R3-MYB, CsMYB34, as a critical gene specifically regulating galloylated catechin biosynthesis. CsMYB34 has a TT2-type motif [VIRTKATRCSKVFIP]. Its transcription levels were positively correlated with galloylated catechin content in 19 tea varieties, with correlation coefficients ≥0.79. Suppression of CsMYB34 expression caused a significant decrease in galloylated catechin content, as well as reduced expression levels of the key galloylated catechin biosynthesis gene CsSCPL4. Yeast one-hybrid (Y1H), electrophoretic mobile shift assay (EMSA) and dual-luciferase reporter system (DLR) showed that CsMYB34 interacts directly with the promoter region of CsSCPL4, thereby upregulating its transcription. This research indicates that the CsMYB34 transcription factor selectively modulates the biosynthetic pathway of galloylated catechins, thereby offering a plausible rationale for the observed elevated levels of these compounds in tea leaves
Beschreibung:Date Revised 19.12.2024
published: Print-Electronic
Citation Status Publisher
ISSN:1873-2690
DOI:10.1016/j.plaphy.2024.109401