Molecular cloning and expression analysis of iridoid synthase genes from Rehmannia glutinosa.
10.19540/j.cnki.cjcmm.20190325.103
- Author:
Chao-Fei YANG
1
;
Xin-Rong LI
1
;
Jing-Yu ZHI
1
;
Xiao-Tong GENG
2
;
Li-Ya HONG
1
;
Feng-Qing WANG
1
;
Cai-Xia XIE
2
Author Information
1. College of Agronomy,Henan Agricultural University Zhengzhou 450002,China.
2. School of medicine,Henan University of Chinese Medicine Zhengzhou 450046,China.
- Publication Type:Journal Article
- Keywords:
Rehmannia glutinosa;
cloning;
expression characterization;
iridoid synthase gene;
sequence analysis
- MeSH:
Cloning, Molecular;
Genes, Plant;
Iridoids;
metabolism;
Ligases;
genetics;
Phylogeny;
Rehmannia;
enzymology;
genetics
- From:
China Journal of Chinese Materia Medica
2019;44(12):2472-2479
- CountryChina
- Language:Chinese
-
Abstract:
Iridoid synthase( IS),the key enzyme in the natural biosynthesis of vegetal iridoids,catalyzes the irreversible cyclization of 10-oxogeranial to epi-iridodial. In this study,we screened the Rehmannia glutinosa transcriptome data by BLASTn with Catharanthus roseus CrIS cDNA,and found four c DNA fragments with length of 1 527,1 743,1 425,1 718 bp,named RgIS1,RgIS2,RgIS3 and RgIS4,respectively. Bioinformatics analysis revealed that the four iridoid synthase genes encoding proteins with 389-392 amino acid residues,protein molecular weights were between 44. 30-44. 74 k Da,and theoretical isoelectric points were between 5. 30 and 5. 87. Subcellular localization predictions showed that the four iridoid synthase were distributed in the cytoplasm. Structure analysis revealed that R. glutinosa iridoid synthases contain six conserved short-chain dehydrogenase/reductase( SDR) motifs,and their 3 D models were composed typical dinucleotide-binding " Rossmann" folds covered by helical C-terminal extensions. Using the amino acid sequences of four R. glutinosa iridoid synthases,phylogenetic analysis was performed,the result indicated that RgIS3,CrIS and Olea europaea OeIS were grouped together,the other R. glutinosa iridoid synthases and fifteen proteins in other plants had close relationship. Real-time fluorescent quantitative PCR revealed that RgIS1 and RgIS3 highly expressed in unfold leaves,however,RgIS2 and RgIS4 highly expressed in stems and tuberous roots,respectively. RgIS3 showed higher expression levels in non-radial striations( nRS) of the two cultivars,and RgIS1 and RgIS2 had higher expression levels in nRS of QH,while RgIS4 had less expression levels in nRS of QH1. RgIS1,RgIS2 and RgIS3 were up-regulated by Me JA treatment,although the time and degree of response differed. Our findings are helpful to reveal molecular function of R. glutinosa iridoid synthases and provide a clue for studing the molecular mechanism of iridoid biosynthesis.
