Cloning and Characterization of Two cDNA Sequences Coding Squalene Synthase Involved in Glycyrrhizic Acid Biosynthesis in Glycyrrhiza uralensis

Author(s):  
Ying Liu ◽  
Ning Zhang ◽  
Honghao Chen ◽  
Ya Gao ◽  
Hao Wen ◽  
...  
2021 ◽  
Author(s):  
Junping He ◽  
Lu Yao ◽  
Juan Wang ◽  
Wenyuan Gao

Abstract In order to better understand the mechanism of glycyrrhizic acid biosynthesis and explore important enzyme gene resources in Glycyrrhiza uralensis Fisch., we sequenced the transcriptome of the adventitious roots of G. uralensis treated by methyl jasmonate (MJ) and assembled the de novo sequence. 256503 unique transcripts with an average length of 898bp were produced. Transcriptome sequencing and data analysis showed that the key genes of glycyrrhizic acid biosynthesis changed significantly after MJ treatment. 2720 up-regulated genes and 3493 down regulated genes were found. In the process of oxidation and glycosylation of glycyrrhizic acid biosynthesis. A putative CYP450 gene (Cluster-30944.70498) is positively correlated with glycyrrhetinic acid. The glycosyltransferase gene (Cluster-30944.25725) is positively correlated with glycyrrhizic acid and glycyrrhetinic acid. In addition, we found an AP2-EREBP family transcription factor (Cluster-30944.55070). It had high amino acid sequence similarity with PgERF1. In Panax ginseng, PgERF1 was identified as promoting the biosynthesis of triterpenoid saponins. According to the correlation analysis of transcription factors, functional gene expression and component accumulation, we speculated that this transcription factor can positively regulate the expression of farnesyl diphosphate, squalene epoxide and glycosyltransferase (Cluster-30944.25725) genes and ultimately increase the content of glycyrrhizic acid.


2016 ◽  
Vol 18 (5) ◽  
pp. 445-455 ◽  
Author(s):  
Panpan Zhang ◽  
Xiaoying Cao ◽  
Changgen Li ◽  
Zhujun Zheng ◽  
Sun Yong ◽  
...  

Biologia ◽  
2021 ◽  
Author(s):  
Zahra Shirazi ◽  
Samaneh Samavat ◽  
Mahnaz Nezamivand Chegini ◽  
Yousef Mohammadi ◽  
Farzad Banaei-Asl

Genome ◽  
2009 ◽  
Vol 52 (7) ◽  
pp. 647-657 ◽  
Author(s):  
P. J. Maughan ◽  
T. B. Turner ◽  
C. E. Coleman ◽  
D. B. Elzinga ◽  
E. N. Jellen ◽  
...  

Salt tolerance is an agronomically important trait that affects plant species around the globe. The Salt Overly Sensitive 1 (SOS1) gene encodes a plasma membrane Na+/H+ antiporter that plays an important role in germination and growth of plants in saline environments. Quinoa (Chenopodium quinoa Willd.) is a halophytic, allotetraploid grain crop of the family Amaranthaceae with impressive nutritional content and an increasing worldwide market. Many quinoa varieties have considerable salt tolerance, and research suggests quinoa may utilize novel mechanisms to confer salt tolerance. Here we report the cloning and characterization of two homoeologous SOS1 loci (cqSOS1A and cqSOS1B) from C. quinoa, including full-length cDNA sequences, genomic sequences, relative expression levels, fluorescent in situ hybridization (FISH) analysis, and a phylogenetic analysis of SOS1 genes from 13 plant taxa. The cqSOS1A and cqSOS1B genes each span 23 exons spread over 3477 bp and 3486 bp of coding sequence, respectively. These sequences share a high level of similarity with SOS1 homologs of other species and contain two conserved domains, a Nhap cation-antiporter domain and a cyclic-nucleotide binding domain. Genomic sequence analysis of two BAC clones (98 357 bp and 132 770 bp) containing the homoeologous SOS1 genes suggests possible conservation of synteny across the C. quinoa sub-genomes. This report represents the first molecular characterization of salt-tolerance genes in a halophytic species in the Amaranthaceae as well as the first comparative analysis of coding and non-coding DNA sequences of the two homoeologous genomes of C. quinoa.


Biofouling ◽  
2017 ◽  
Vol 34 (1) ◽  
pp. 1-14 ◽  
Author(s):  
Xiaochun Huang ◽  
Chang Chen ◽  
Chunhua Ren ◽  
Yingying Li ◽  
Yiqin Deng ◽  
...  

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