Identification of Lonicera japonica TPS gene family and expression analysis under aphid damage.
10.19540/j.cnki.cjcmm.20250114.102
- Author:
Gang WANG
1
;
Yuan CUI
2
;
Qi-Dong LI
1
;
Lu-Yao HUANG
1
;
Zhen-Hua LIU
1
;
Jia LI
1
Author Information
1. College of Pharmacy, Shandong University of Traditional Chinese Medicine Ji'nan 250355, China.
2. Ji'nan Agricultural Technology Extension and Service Center Ji'nan 250004, China.
- Publication Type:Journal Article
- Keywords:
Lonicera japonica;
aphid stress;
bioinformatics analysis;
terpene synthase(TPS)
- MeSH:
Animals;
Aphids/physiology*;
Alkyl and Aryl Transferases/chemistry*;
Lonicera/parasitology*;
Phylogeny;
Plant Proteins/chemistry*;
Gene Expression Regulation, Plant;
Multigene Family;
Terpenes/metabolism*
- From:
China Journal of Chinese Materia Medica
2025;50(8):2116-2129
- CountryChina
- Language:Chinese
-
Abstract:
This study explores the basic characteristics and potential functions of the terpene synthase(TPS) gene family members in Lonicera japonica. The L. japonica TPS(LjTPS) gene family was identified and functionally analyzed using bioinformatics methods. The results showed that a total of 70 members of the LjTPS gene family were identified in L. japonica, with protein lengths ranging from 130 to 1 437 amino acids. Most of these proteins were hydrophilic, and they were unevenly distributed across nine chromosomes. Phylogenetic analysis showed that the LjTPS gene family members were divided into six subfamilies, mainly consisting of members from the TPS-a, TPS-b, and TPS-e subfamilies. Promoter cis-acting element analysis showed that LjTPS members contained a large number of stress-responsive cis-acting elements. Aphid inoculation experiments showed that key enzyme genes in the MVA pathway for terpenoid backbone synthesis in L. japonica, such as HMGS, HMGR, MK, MPD, and the key enzyme gene in the DXP pathway, DXS, exhibited an initial increase followed by a decrease under aphid stress. The qRT-PCR analysis showed that the expression levels of the α-farnesene synthase genes LjTPS34 and LjTPS39 were down-regulated, while the expression levels of(E)-β-caryophyllene synthase genes LjTPS15 and LjTPS17 were up-regulated 12 h before aphid feeding, then began to decline. Farnesyl pyrophosphate synthase(FPS), which interacted with these genes, also displayed a pattern of increasing followed by decreasing expression. The expression of linalool synthase genes LjTPS12 and LjTPS33 was significantly up-regulated after 72 h of aphid feeding(P<0.000 1), reaching 24.39 and 22.64 times the initial expression, respectively. This pattern was in close alignment with the trend of linalool content in L. japonica. This study provides a theoretical foundation for future research on the interaction between L. japonica and pests, as well as on the functional roles of the LjTPS gene family.
