College of Horticulture and Gardening, Yangtze University, Jingzhou 434025, China.
Plant Physiol. 2024 May 31;195(2):1446-1460. doi: 10.1093/plphys/kiae114.
Terpene trilactones (TTLs) are important secondary metabolites in ginkgo (Ginkgo biloba); however, their biosynthesis gene regulatory network remains unclear. Here, we isolated a G. biloba ethylene response factor 4 (GbERF4) involved in TTL synthesis. Overexpression of GbERF4 in tobacco (Nicotiana tabacum) significantly increased terpenoid content and upregulated the expression of key enzyme genes (3-hydroxy-3-methylglutaryl-CoA reductase [HMGR], 3-hydroxy-3-methylglutaryl-CoA synthase [HMGS], 1-deoxy-D-xylulose-5-phosphate reductoisomerase [DXR], 1-deoxy-D-xylulose-5-phosphate synthase [DXS], acetyl-CoA C-acetyltransferase [AACT], and geranylgeranyl diphosphate synthase [GGPPS]) in the terpenoid pathway in tobacco, suggesting that GbERF4 functions in regulating the synthesis of terpenoids. The expression pattern analysis and previous microRNA (miRNA) sequencing showed that gb-miR160 negatively regulates the biosynthesis of TTLs. Transgenic experiments showed that overexpression of gb-miR160 could significantly inhibit the accumulation of terpenoids in tobacco. Targeted inhibition and dual-luciferase reporter assays confirmed that gb-miR160 targets and negatively regulates GbERF4. Transient overexpression of GbERF4 increased TTL content in G. biloba, and further transcriptome analysis revealed that DXS, HMGS, CYPs, and transcription factor genes were upregulated. In addition, yeast 1-hybrid and dual-luciferase reporter assays showed that GbERF4 could bind to the promoters of the HMGS1, AACT1, DXS1, levopimaradiene synthase (LPS2), and GGPPS2 genes in the TTL biosynthesis pathway and activate their expression. In summary, this study investigated the molecular mechanism of the gb-miR160-GbERF4 regulatory module in regulating the biosynthesis of TTLs. It provides information for enriching the understanding of the regulatory network of TTL biosynthesis and offers important gene resources for the genetic improvement of G. biloba with high contents of TTLs.
三萜类内酯(TTLs)是银杏(Ginkgo biloba)中的重要次生代谢产物;然而,其生物合成基因调控网络尚不清楚。在这里,我们分离出一个参与 TTL 合成的银杏乙烯反应因子 4(GbERF4)。GbERF4 在烟草(Nicotiana tabacum)中的过表达显著增加了萜类化合物的含量,并上调了关键酶基因(3-羟基-3-甲基戊二酰基辅酶 A 还原酶[HMGR]、3-羟基-3-甲基戊二酰基辅酶 A 合酶[HMGS]、1-脱氧-D-木酮糖-5-磷酸还原异构酶[DXR]、1-脱氧-D-木酮糖-5-磷酸合酶[DXS]、乙酰辅酶 A C-乙酰转移酶[AACT]和香叶基香叶基二磷酸合酶[GGPPS])在烟草萜类途径中的表达,表明 GbERF4 功能在于调节萜类化合物的合成。表达模式分析和先前的 microRNA(miRNA)测序表明,gb-miR160 负调控 TTLs 的生物合成。转基因实验表明,gb-miR160 的过表达可显著抑制烟草萜类化合物的积累。靶标抑制和双荧光素酶报告基因测定证实,gb-miR160 靶向并负调控 GbERF4。GbERF4 的瞬时过表达增加了银杏中的 TTL 含量,进一步的转录组分析表明 DXS、HMGS、CYPs 和转录因子基因上调。此外,酵母 1 杂交和双荧光素酶报告基因测定表明,GbERF4 可以与 TTL 生物合成途径中的 HMGS1、AACT1、DXS1、左旋蒎烯合酶(LPS2)和 GGPPS2 基因的启动子结合并激活它们的表达。综上所述,本研究探讨了 gb-miR160-GbERF4 调控模块在调节 TTL 生物合成中的分子机制。它为丰富 TTL 生物合成调控网络的认识提供了信息,并为具有高 TTL 含量的银杏遗传改良提供了重要的基因资源。