» Articles » PMID: 19857882

Regulation of Ginsenoside and Phytosterol Biosynthesis by RNA Interferences of Squalene Epoxidase Gene in Panax Ginseng

Overview
Journal Phytochemistry
Publisher Elsevier
Date 2009 Oct 28
PMID 19857882
Citations 75
Authors
Affiliations
Soon will be listed here.
Abstract

Squalene epoxidase catalyzes the first oxygenation step in phytosterol and triterpenoid saponin biosynthesis and is suggested to represent one of the rate-limiting enzymes in this pathway. Here, we investigated the roles of two squalene epoxidase genes (PgSQE1 and PgSQE2) in triterpene and phytosterol biosynthesis in Panax ginseng. PgSQE1 and PgSQE2 encoded deduced proteins of 537 and 545 amino acids, respectively. Amino acid sequences deduced from PgSQE1 and PgSQE2 share 83% homology, but the N-terminal regions (first 60 amino acids) are highly different. PgSQE1 mRNA abundantly accumulated in all organs. PgSQE2 was only weakly expressed and preferentially in petioles and flower buds. Methyl jasmonate (MeJA) treatment enhanced the accumulation of PgSQE1 mRNA in roots, but rather suppressed expression of PgSQE2. Precursor (squalene) treatment coordinately upregulated the expression of both PgSQE1 and PgSQE2. In situ hybridization analysis established that both PgSQE1 and PgSQE2 mRNAs accumulated preferentially in vascular bundle tissue and resin ducts of petioles. RNA interference of PgSQE1 in transgenic P. ginseng completely suppressed PgSQE1 transcription. Concomitantly, the interference of PgSQE1 resulted in reduction of ginsenoside production. Interestingly, silencing of PgSQE1 in RNAi roots strongly upregulated PgSQE2 and PNX (cycloartenol synthase) and resulted in enhanced phytosterol accumulation. These results indicate that expression of PgSQE1 and PgSQE2 were regulated in a different manner, and that PgSQE1 will regulate ginsenoside biosynthesis, but not that of phytosterols in P. ginseng.

Citing Articles

Interactions between arbuscular mycorrhizal fungi and phosphate-soluble bacteria affect ginsenoside compositions by modulating the C:N:P stoichiometry in .

Mu P, Ding G, Zhang Y, Jin Q, Liu Z, Guan Y Front Microbiol. 2024; 15:1426440.

PMID: 39417075 PMC: 11479886. DOI: 10.3389/fmicb.2024.1426440.


Identification of Gene for Ginsenoside Rg1 Biosynthesis as Revealed by Combining Genome-Wide Association Study and Gene Co-Expression Network Analysis of Jilin Ginseng Core Collection.

Liu S, Chen X, Zhao T, Yu J, Chen P, Wang Y Plants (Basel). 2024; 13(13).

PMID: 38999623 PMC: 11244481. DOI: 10.3390/plants13131784.


Functional Validation of the Cytochrome P450 Family Gene in .

Jiang Y, He G, Li R, Wang K, Wang Y, Zhao M Biomolecules. 2024; 14(6).

PMID: 38927118 PMC: 11201774. DOI: 10.3390/biom14060715.


Telomere-to-telomere reference genome for highlights the evolution of saponin biosynthesis.

Song Y, Zhang Y, Wang X, Yu X, Liao Y, Zhang H Hortic Res. 2024; 11(6):uhae107.

PMID: 38883331 PMC: 11179851. DOI: 10.1093/hr/uhae107.


RNA sequencing analysis reveals as the key regulator in response to methyl jasmonate-induced saponin accumulation in .

Zhang W, Zhang J, Fan Y, Dong J, Gao P, Jiang W Hortic Res. 2024; 11(5):uhae058.

PMID: 38716227 PMC: 11070725. DOI: 10.1093/hr/uhae058.