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volume 16 issue 3 pages 393

Phenotypic and RNA-seq Profiles Identified Key Pathways and Genes Involved in Gleditsioside Biosynthesis in Gleditsia sinensis Lam.

Jing Wang 1, 2
Yuzhang Yang 1
Yanping Liu 2
Jiahao Liu 1
Dandan Xiao 1
Hui Chen 1
Chun Wang 1
Tiantian Fu 1
Fuli Chang 3
Yanwei Wang 1
Dingchen Fan 2
Publication typeJournal Article
Publication date2025-02-22
scimago Q1
wos Q2
SJR0.600
CiteScore4.6
Impact factor2.5
ISSN19994907
Abstract

Gleditsia sinensis Lam. (G. sinensis) is a widely known medicinal plant, and its primary bioactive compound is gleditsioside. So far, the significant economic and medicinal value of gleditsioside has been widely recognized. However, the transcriptional regulation governing the biosynthesis of gleditsioside during G. sinensis pod development remains unclear. In this investigation, we observed that gleditsioside levels increased in the pods of G. sinensis from June to November, and we performed a transcriptome analysis to explore the phenomenon. A total of 703 and 162 differentially expressed unigenes (DEGs) were identified in the terpenoid backbone and triterpenoid biosynthesis pathways, respectively. In total, 99 unigenes encoding 17 enzymes, such as ENIN, cytochrome P450 (CYP93E1), and UDP-glucosyltransferase, were identified in the gleditsioside biosynthesis pathway. Moreover, DEGs encoding crucial enzymes, such as HMGCR and AGBH, might determine gleditsioside synthesis during G. sinensis pod development. Interestingly, the gleditsioside synthesis pathway extended to ten metabolic pathways, including the sterol biosynthesis pathway and the brassinolide biosynthesis pathway, among other pathways involved in various hormonal regulations. These pathways shared the same precursor substances (IPP and DMAPP). In addition, weighted gene correlation network analysis (WGCNA) revealed that CL5845.Contig1 (HMGCR) and CL8823.Contig2 (LUP4) might be involved in the gleditsioside biosynthesis. Furthermore, transient transformation validation experiments demonstrated overexpression of CL5845.Contig1 (HMGCR), CL8823.Contig2 (LUP4), and CL11248.Contig4 (CYP93E1) significantly enhanced gleditsioside biosynthesis. Overall, our findings provide important genetic resources for future functional research and new insights into the basic mechanism of saponin biosynthesis.

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Wang J. et al. Phenotypic and RNA-seq Profiles Identified Key Pathways and Genes Involved in Gleditsioside Biosynthesis in Gleditsia sinensis Lam. // Forests. 2025. Vol. 16. No. 3. p. 393.
GOST all authors (up to 50) Copy
Wang J., Yang Y., Liu Y., Liu J., Xiao D., Chen H., Wang C., Fu T., Chang F., Wang Y., Fan D. Phenotypic and RNA-seq Profiles Identified Key Pathways and Genes Involved in Gleditsioside Biosynthesis in Gleditsia sinensis Lam. // Forests. 2025. Vol. 16. No. 3. p. 393.
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TY - JOUR
DO - 10.3390/f16030393
UR - https://www.mdpi.com/1999-4907/16/3/393
TI - Phenotypic and RNA-seq Profiles Identified Key Pathways and Genes Involved in Gleditsioside Biosynthesis in Gleditsia sinensis Lam.
T2 - Forests
AU - Wang, Jing
AU - Yang, Yuzhang
AU - Liu, Yanping
AU - Liu, Jiahao
AU - Xiao, Dandan
AU - Chen, Hui
AU - Wang, Chun
AU - Fu, Tiantian
AU - Chang, Fuli
AU - Wang, Yanwei
AU - Fan, Dingchen
PY - 2025
DA - 2025/02/22
PB - MDPI
SP - 393
IS - 3
VL - 16
SN - 1999-4907
ER -
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@article{2025_Wang,
author = {Jing Wang and Yuzhang Yang and Yanping Liu and Jiahao Liu and Dandan Xiao and Hui Chen and Chun Wang and Tiantian Fu and Fuli Chang and Yanwei Wang and Dingchen Fan},
title = {Phenotypic and RNA-seq Profiles Identified Key Pathways and Genes Involved in Gleditsioside Biosynthesis in Gleditsia sinensis Lam.},
journal = {Forests},
year = {2025},
volume = {16},
publisher = {MDPI},
month = {feb},
url = {https://www.mdpi.com/1999-4907/16/3/393},
number = {3},
pages = {393},
doi = {10.3390/f16030393}
}
MLA
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Wang, Jing, et al. “Phenotypic and RNA-seq Profiles Identified Key Pathways and Genes Involved in Gleditsioside Biosynthesis in Gleditsia sinensis Lam..” Forests, vol. 16, no. 3, Feb. 2025, p. 393. https://www.mdpi.com/1999-4907/16/3/393.