Cloning and expression characteristics of a transcription factor gene RpMYB4 in Rheum palmatum L.
10.16438/j.0513-4870.2020-1654
- VernacularTitle:掌叶大黄转录因子RpMYB4基因克隆及分子表达特性
- Author:
Yuan-min LI
1
;
Na ZHANG
1
,
2
;
Hui LI
1
;
Ming-ying ZHANG
1
;
Liang PENG
1
;
Yong-gang YAN
1
;
Yi-min LI
1
;
Gang ZHANG
1
Author Information
1. Shaanxi University of Chinese Medicine of Pharmacy/Shaanxi Qinling Chinese Herbal Medicine Application Development Engineering Technology Research Center, Xi'an 712046, China
2. Shaanxi TianQi Biotechnology Limited Liability Company, Yulin 718400, China
- Publication Type:Research Article
- Keywords:
italic>Rheum palmatum L.;
transcription factor;
MYB;
gene expression;
stress
- From:
Acta Pharmaceutica Sinica
2021;56(4):1170-1177
- CountryChina
- Language:Chinese
-
Abstract:
MYB transcription factors play many important regulatory roles in plant growth and development, secondary metabolism, and stress adaptation processes. In this work, an MYB gene containing a complete open reading frame (ORF) was selected from the transcriptome database of R. palmatum L. RpMYB4 ORF and cloned, encoding a polypeptide of 245 amino acids with a molecular weight of 26.99 kDa. RpMYB4 lacks a signal peptide or transmembrane domain but contains two conserved DNA binding domains (HTH-MYB) of the R2R3-MYB subfamily at the N-terminus. Multiple-sequence alignment demonstrated that RpMYB4 shared as high as 61% identity with many MYB proteins from other species. Phylogenetic analysis showed that RpMYB4 had the closest relationship with FtMYB8 and was clustered in the S4 subfamily. Subcellular localization by confocal microscopy showed that an RpMYB4-GFP-fusion protein localized to the nucleus in tobacco. Real-time fluorescence quantitative PCR analyses revealed that RpMYB4 was differentially expressed in various tissues, with the highest expression in leaves, followed by petioles, rhizome, and roots, and with the lowest level in mature seeds. After treatment of R. palmatum L. seedlings with 200 μmol·L-1 MeJA, the expression of RpMYB4 in leaves was down-regulated within 24 h, and significantly up-regulated after 200 μmol·L-1 SA treatment at 12 h and 24 h. However, gene expression did not change with 200 μmol·L-1 ABA treatment. The transcripts of RpMYB4 under drought, high temperature, and mechanical injury stresses reached a peak at 24 h, 24 h, and at 3 h, respectively, while RpMYB4 expression was inhibited by low temperature stress, reaching its lowest value at 6 h. The gene showed no significant response to salt stress. Overall, RpMYB4 was cloned from R. palmatum L. for the first time, showed high expression in leaves, and was responsive to SA and various abiotic stress treatments including drought, high temperature, and mechanical injury. The results will be useful for further analysis of secondary metabolism and stress adaptations in R. palmatum L.
