Elucidating the mechanisms underlying differential anthocyanin biosynthesis and its link to stem color and root isoflavonoid levels in Astragalus membranaceus var. mongholicus

Yi Chen , Sifei Duan , Meng Zhang , Yang-oujie Bao , Yungang Tian , Xuehui Dong , Min Ye

Horticulture Research ›› 2026, Vol. 13 ›› Issue (6) : 88

PDF (8351KB)
Horticulture Research ›› 2026, Vol. 13 ›› Issue (6) :88 DOI: 10.1093/hr/uhag088
Article
research-article
Elucidating the mechanisms underlying differential anthocyanin biosynthesis and its link to stem color and root isoflavonoid levels in Astragalus membranaceus var. mongholicus
Author information +
History +
PDF (8351KB)

Abstract

Astragalus membranaceus var. mongholicus (AMM) is the principal botanical source of Huangqi, a traditional medicinal herb whose therapeutic value primarily stems from the accumulation of isoflavones and other bioactive compounds in the roots. In this study, field surveys across major AMM production regions revealed pronounced natural variation in stem coloration. Chemical analysis showed that the roots of the red-stemmed type contained significantly higher levels of four bioactive isoflavones and volatile organic compounds than those in green-stemmed plants. Metabolomic profiling further revealed a specific enrichment of cyanidin-based anthocyanins in the red stems, establishing the metabolic basis of the red stem phenotype. Both transcriptomic and metabolomic analyses indicated an overall upregulation of the flavonoid and phenylpropanoid biosynthetic pathways in the stem and root tissues of red-stemmed AMM. Weighted gene co-expression network analysis (WGCNA) identified six key genes ( AmC4H, AmCHS, AmCHI, AmF3H, AmF3′H, and AmBZ1) that were strongly associated with the red stem phenotype, all of which were specifically highly expressed in red stems. Functional assays confirmed their roles in anthocyanin biosynthesis. Molecular modeling provided further insights into the substrate specificity of AmBZ1. This study proposes stem color as a visible phenotypic reference for early-stage germplasm selection in AMM, and characterizes the molecular basis underlying red stem formation, providing a foundation for elite germplasm development and molecular breeding.

Cite this article

Download citation ▾
Yi Chen, Sifei Duan, Meng Zhang, Yang-oujie Bao, Yungang Tian, Xuehui Dong, Min Ye. Elucidating the mechanisms underlying differential anthocyanin biosynthesis and its link to stem color and root isoflavonoid levels in Astragalus membranaceus var. mongholicus. Horticulture Research, 2026, 13 (6) : 88 DOI:10.1093/hr/uhag088

登录浏览全文

4963

注册一个新账户 忘记密码

Acknowledgements

This work was supported by National Natural Science Foundation of China (no. 81891011), National Key Research and Development Program of China (no. 2023YFA0914100), and China Postdoctoral Science Foundation (no. 2025M773890).

Author contributions

M.Y., and X.D. designed the study. Y.C., and S.D. prepared the samples. Y.T. established the HPLC-UV quantitative method for the four isoflavones. Y.C. performed most of the experiments. M.Z. performed the molecular docking of AmBZ1; Y.C., and S.D. analyzed the data. M.Z.; Y.C. wrote the manuscript. M.Z., Y.B., and M.Y. revised the manuscript.

Data availability

The raw transcriptome sequencing data have been deposited into the China National Center for Bioinformation (CNCB) at the following URL: http://www.gpgenome.com/species/109.

Conflicts of interest statement

The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

References

[1]

Fu J, Wang Z, Huang L, et al. Review of the botanical characteristics, phytochemistry, and pharmacology of Astragalus membranaceus (Huangqi) . Phytother Res. 2014; 28: 1275-83

[2]

Wang P, Wang Z, Zhang Z, et al. A review of the botany, phytochemistry, traditional uses, pharmacology, toxicology, and quality control of the Astragalus memeranaceus . Front Pharmacol. 2023; 14: 1242318

[3]

Durazzo A, Nazhand A, Lucarini M, et al. Astragalus (Astragalus membranaceus Bunge): botanical, geographical, and historical aspects to pharmaceutical components and beneficial role . Rend Fis Acc Lincei. 2021; 32: 625-42

[4]

Li J, Xu L, Sang R, et al. Immunomodulatory and anti-inflammatory effects of total flavonoids of Astragalus by regulating NF-KB and MAPK signalling pathways in RAW 264.7 macrophages . Pharmazie. 2018; 73: 589-93

[5]

Zheng Y, Ren W, Zhang L, et al. A review of the pharmacological action of Astragalus polysaccharide . Front Pharmacol. 2020; 11: 349

[6]

Yeh T, Chuang H, Huang W, et al. Astragalus membranaceus improves exercise performance and ameliorates exercise-induced fatigue in trained mice . Molecules. 2014; 19: 2793-807

[7]

Zhang J, Qiao Y, Li D, et al. Aqueous extract from Astragalus membranaceus can improve the function degradation and delay aging on Drosophila melanogaster through antioxidant mechanism . Rejuvenation Res. 2022; 25: 181-90

[8]

Li Y, Duan B, Li Y, et al. The isoflavonoid calycosin inhibits inflammation and enhances beta cell function in gestational diabetes mellitus by suppressing RNF38 expression. Immunopharmacol Immunotoxicol. 2020; 42: 366-72

[9]

Liu P, Zhao H, Luo Y . Anti-aging implications of Astragalus membranaceus (Huangqi): a well-known Chinese tonic . Aging Dis. 2017; 8: 868-86

[10]

Li B, Wang F, Liu N, et al. Astragaloside IV inhibits progression of glioma via blocking MAPK/ERK signaling pathway. Biochem Biophys Res Commun. 2017; 491: 98-103

[11]

Li W, Song K, Wang S, et al. Anti-tumor potential of astragalus polysaccharides on breast cancer cell line mediated by macrophage activation. Mater Sci Eng C Mater Biol Appl. 2019; 98: 685-95

[12]

Chen Z, Liu L, Gao C, et al. Astragali radix (Huangqi): a promising edible immunomodulatory herbal medicine. J Ethnopharmacol. 2020; 258: 112895

[13]

Farag M, Alagawany M . The role of Astragalus membranaceus as immunomodulator in poultry . World Poult Sci J. 2019; 75: 43-54

[14]

Chen K, Zhang M, Xu L, et al. Identification of oxidosqualene cyclases associated with saponin biosynthesis from Astragalus membranaceus reveals a conserved motif important for catalytic function . J Adv Res. 2023; 43: 247-57

[15]

Wu X, Li X, Wang W, et al. Integrated metabolomics and transcriptomics study of traditional herb Astragalus membranaceus Bge. var. mongolicus (Bge.) Hsiao reveals global metabolic profile and novel phytochemical ingredients . BMC Genomics. 2020; 21: 697

[16]

Xu B, Huang J, Peng G, et al. Total biosynthesis of the medicinal triterpenoid saponin astragalosides. Nat Plants. 2024; 10: 1826-37

[17]

Zhang M, Yi Y, Gao B, et al. Functional characterization and protein engineering of a triterpene 3-/6-/2’- O-glycosyl transferase reveal a conserved residue critical for the regiospecificity . Angew Chem Int Ed. 2022; 61: e202113587

[18]

Zhao Y, Liu G, Yang F, et al. Multilayered regulation of secondary metabolism in medicinal plants. Mol Hortic. 2023; 3: 11

[19]

Yang W, Su Y, Dong G, et al. Liquid chromatography-mass spectrometry-based metabolomics analysis of flavonoids and anthraquinones in Fagopyrum tataricum L. Gaertn. (tartary buckwheat) seeds to trace morphological variations . Food Chem. 2020; 31: 127354

[20]

Tanaka Y, Sasaki N, Ohmiya A . Biosynthesis of plant pigments: anthocyanins, betalains and carotenoids. Plant J. 2008; 54: 733-49

[21]

He G, Zhang R, Jiang S, et al. The MYB transcription factor RcMYB1 plays a central role in rose anthocyanin biosynthesis. Hortic Res. 2023; 10: uhad080

[22]

Yan Y, Zhao J, Lin S, et al. Light-mediated anthocyanin biosynthesis in rose petals involves a balanced regulatory module comprising transcription factors RhHY5, RhMYB114a, and RhMYB3b. J Exp Bot. 2023; 74: 5783-804

[23]

Kachanovsky D, Filler S, Isaacson T, et al. Epistasis in tomato color mutations involves regulation of phytoene synthase 1 expression by cis-carotenoids . Proc Natl Acad Sci USA. 2012; 109: 19021-6

[24]

Winkel-Shirley B. Flavonoid biosynthesis. A colorful model for genetics, biochemistry, cell biology, and biotechnology. Plant Physiol. 2001; 126: 485-93

[25]

Amato A, Cavallini E, Walker A, et al. The MYB5-driven MBW complex recruits a WRKY factor to enhance the expression of targets involved in vacuolar hyper-acidification and trafficking in grapevine. Plant J. 2019; 99: 1220-41

[26]

Kaur S, Sharma N, Kapoor P, et al. Spotlight on the overlapping routes and partners for anthocyanin transport in plants. Physiol Plant. 2021; 171: 868-81

[27]

Zhou H, He J, Zhang Y, et al. RHA2b-mediated MYB30 degradation facilitates MYB75-regulated, sucrose-induced anthocyanin biosynthesis in Arabidopsis seedlings . Plant Commun. 2024; 5: 100744

[28]

Sun H, Xie D, Guo X, et al. Study on the relevance between beany flavor and main bioactive components in Radix Astragali. J Agric Food Chem. 2010; 58: 5568-73

[29]

Abramson J, Adler J, Dunger J, et al. Accurate structure prediction of biomolecular interactions with AlphaFold 3. Nature. 2024; 630: 493-500

[30]

Shen S, Zhan C, Yang C, et al. Metabolomics-centered mining of plant metabolic diversity and function: past decade and future perspectives. Mol Plant. 2023; 16: 43-63

[31]

Li Z, Rubert-Nason K, Jamieson M, et al. Root secondary metabolites in Populus tremuloides: effects of simulated climate warming, defoliation, and genotype . J Chem Ecol. 2021; 47: 313-21

[32]

Su Y, Zhang J, Xu Z, et al. Integrative analysis of metabolome and transcriptome reveals the mechanism of color formation in white root (Salvia miltiorrhiza) . Ind Crop Prod. 2021; 170: 113784

[33]

Jiang D, Lin H, Liu Z, et al. Polyacetylenes and sesquiterpenes in Chinese traditional herb Atractylodes lancea: biomarkers and synergistic effects in red secretory cavities . Mol Hortic. 2025; 5: 11

[34]

Grotewold E. The genetics and biochemistry of floral pigments. Annu Rev Plant Biol. 2006; 57: 761-80

[35]

Zeng H, Zheng T, Tang Q, et al. Integrative metabolome and transcriptome analyses reveal the coloration mechanism in Camellia oleifera petals with different color . BMC Plant Biol. 2024; 24: 19

[36]

Chen Z, Shah F, Lu X, et al. The ApWRKY26/ApERF4-ApMYB2 module regulates anthocyanin accumulation for the seasonal leaf color transition in Acer palmatum . Hortic Res. 2025; 13: uhaf257

[37]

Koes R, Verweij W, Quattrocchio F . Flavonoids: a colorful model for the regulation and evolution of biochemical pathways. Trends Plant Sci. 2005; 10: 236-42

[38]

Lam P, Wang L, Lui A, et al. Deficiency in flavonoid biosynthesis genes CHS, CHI, and CHIL alters rice flavonoid and lignin profiles . Plant Physiol. 2022; 188: 1993-2011

[39]

Xu W, Dubos C, Lepiniec L . Transcriptional control of flavonoid biosynthesis by MYB-bHLH-WDR complexes. Trends Plant Sci. 2015; 20: 176-85

[40]

Fang X, Liu H, Liu J, et al. Genome assembly and population genomic analysis reveal the genetic basis of popcorn evolution. Plant Biotechnol J. 2025; 23: 2911-27

[41]

Mouradov A, Spangenberg G . Flavonoids: a metabolic network mediating plants adaptation to their real estate. Front Plant Sci. 2014; 5: 620

[42]

Biała W, Jasiński M . The phenylpropanoid case-it is transport that matters. Front Plant Sci. 2018; 9: 161

[43]

Chen J, Zhang D, Wang Q, et al. Comprehensive comparison of two color varieties of Perillae folium by GC-MS-based metabolomic approach . Molecules. 2022; 27: 6792

[44]

Dossou S, Deng Q, Li F, et al. Metabolic profiling of Perilla leaves of different colors: insights into metabolite variation and bioactive compound distribution. BMC Plant Biol. 2025; 25: 38

[45]

Kaur S, Tiwari V, Kumari A, et al. Protective and defensive role of anthocyanins under plant abiotic and biotic stresses: an emerging application in sustainable agriculture. J Biotechnol. 2023; 361: 12-29

[46]

He J, Giusti M . Anthocyanins: natural colorants with health-promoting properties. Annu Rev Food Sci Technol. 2010; 1: 163-87

[47]

Chen Y, Fang T, Su H, et al. A reference-grade genome assembly for Astragalus mongholicus and insights into the biosynthesis and high accumulation of triterpenoids and flavonoids in its roots . Plant Commun. 2023; 4: 100469

[48]

Trott O, Olson A . AutoDock Vina: improving the speed and accuracy of docking with a new scoring function, efficient optimization and multithreading. J Comput Chem. 2010; 31: 455-61

PDF (8351KB)

115

Accesses

0

Citation

Detail

Sections
Recommended

/