# Heterosis unveiled in root-related traits and saikosaponins content between triploid F1 hybrids and parental Bupleurum chinense DC

**Authors:** Chuanxin Mo, Wenshuai Chen, Zhuolin Lv, Jun Zhao, Yuchan Li, Qiannan Shi, Kaimi Dong, Zhen Wei, Zeru Yu, Xueling Wang, Chao Xin, Zhen Ni, Ma Yu, Hua Chen

PMC · DOI: 10.3389/fpls.2026.1736464 · Frontiers in Plant Science · 2026-02-12

## TL;DR

This study shows that triploid hybrids of Bupleurum chinense have better root growth and higher saikosaponin content than their parents, offering new potential for plant breeding.

## Contribution

The research introduces engineered genomic asymmetry in triploid hybrids to achieve stable and superior heterosis in root traits and bioactive compound yield.

## Key findings

- Triploid hybrids showed 37.3% and 166.5% higher root dry weight than diploid and tetraploid parents.
- Saikosaponin A and D yields increased by 60.7% and 57.5% in hybrids compared to diploid parents.
- Transcriptome analysis linked heterosis to synergistic gene expression in hormone signaling and biosynthesis pathways.

## Abstract

The root biomass and saikosaponins yield of Bupleurum chinense DC. are crucial factors determining its economic value. This study developed triploid F1 hybrid materials of the B. chinense by crossing a diploid (2n=2x1 = 12, x1 = 6) maternal parent with a tetraploid (2n=4x2 = 20, x2 = 5) paternal parent. The resulting hybrids exhibited a stable intergenomic karyotype (2n=x1+2x2 = 16) and significant heterosis. Two-year field trials confirmed strong over-dominance in root architecture, with root dry weight exceeding that of the diploid and tetraploid parents by 37.3% and 166.5%, respectively. The yield of the bioactive compounds saikosaponin A (13.42 mg) and D (13.20 mg) increased by an average of 60.7% and 57.5%, respectively, compared to the diploid parent, highlighting substantial potential for pharmaceutical development. Based on the transcriptome comparison in the seedling and maturity stage of the root, the remarkable heterosis might be supported by unique genomic architecture and sophisticated transcriptional reprogramming. The intergenomic imbalance, likely provide a stable foundation for heterosis by facilitating functional compartmentalization and synergistic interaction between the parental subgenomes. Transcriptome analysis revealed that the heterotic traits were arranged by a complex relationship of gene networks: root morphology was optimized through the additive and transgressive expression of hormone signaling genes, while the enhanced synthesis of saikosaponins was driven by the synergistic expression of key biosynthetic genes. This research provides a novel strategy for exceed conventional plant breeding by demonstrating engineered genomic asymmetry, specifically intergenomic triploid and could help to unlock superior and stable heterosis.

## Linked entities

- **Chemicals:** saikosaponin A (PubChem CID 167928), saikosaponin D (PubChem CID 107793)

## Full-text entities

- **Genes:** CYP71 (cyclophilin71) [NCBI Gene 823585] {aka AtCYP71, cyclophilin 71, cyclophilin71}, PAP2 (phytochrome-associated protein 2) [NCBI Gene 829029] {aka F19B15.110, F19B15_110, IAA27, indole-3-acetic acid inducible 27, phytochrome-associated protein 2}, AT3G07620 (glycosyltransferase) [NCBI Gene 819953], TIR1 (F-box/RNI-like superfamily protein) [NCBI Gene 825473] {aka AtTIR1, TRANSPORT INHIBITOR RESPONSE 1}, MAGO (mago nashi family protein) [NCBI Gene 837560] {aka HAP1, HAPLESS 1, MAGO NASHI, MATERNAL EFFECT EMBRYO ARREST 63, MEE63, T7I23.7}
- **Diseases:** drought (MESH:C536747), Fusarium wilt (MESH:D060585)
- **Chemicals:** vermiculite (MESH:C003760), CBC (MESH:C010695), phosphorus (MESH:D010758), salt (MESH:D012492), glucuronic acid (MESH:D020723), zeatin (MESH:D015026), SA (MESH:D020156), ammonia (MESH:D000641), formamide (MESH:C031066), MVA (MESH:D008798), A+D (-), D (MESH:D003903), ginsenosides (MESH:D036145), scutellarin (MESH:C484876), methanol (MESH:D000432), ABA (MESH:D000040), triterpenes (MESH:D014315), MeJA (MESH:C072239), ETH (MESH:C036216), nitrogen (MESH:D009584), Saikosaponin (MESH:C025759), polyethylene glycol (MESH:D011092), acetyl-CoA (MESH:D000105), Sesquiterpenoid (MESH:D012717), Terpenoid (MESH:D013729), squalene (MESH:D013185), nitrous oxide (MESH:D009609), gibberellin (MESH:D005875), water (MESH:D014867), dextran sulfate (MESH:D016264), tanshinone (MESH:C021751), CTK (MESH:D003583), oleanolic acid (MESH:D009828), 4',6-diamidino-2-phenylindole (MESH:C007293), JA (MESH:C011006), Aux (MESH:D007210), PEG-6000 (MESH:C000595215), 2,3-oxidosqualene (MESH:C002821), GA (MESH:D005708), BR (MESH:D060406), Tween-20 (MESH:D011136), mogroside V (MESH:C041740), IPP (MESH:C004809), acetic acid (MESH:D019342)
- **Species:** Arabidopsis thaliana (mouse-ear cress, species) [taxon 3702], Malus domestica (apple, species) [taxon 3750], Bupleurum falcatum (species) [taxon 46367], Manihot esculenta (cassava, species) [taxon 3983], Glycyrrhiza (licorice, genus) [taxon 46347], watermelon [taxon 260674], Musa acuminata (banana, species) [taxon 4641], Erigeron breviscapus (species) [taxon 244311], Brassica napus var. napus (annual rape, varietas) [taxon 138011], Gypsophila vaccaria (bladder-soapwort, species) [taxon 39387], Musa acuminata AAA Group (Cavendish banana, genotype) [taxon 214697], Platycodon grandiflorus (balloon flower, species) [taxon 94286], Oryza sativa (Asian cultivated rice, species) [taxon 4530], Siraitia grosvenorii (arhat fruit, species) [taxon 190515], Bupleurum chinense (species) [taxon 52451], Eucommia ulmoides (species) [taxon 4392], Panax ginseng (Asiatic ginseng, species) [taxon 4054], Bupleurum scorzonerifolium (species) [taxon 48105], Salvia miltiorrhiza (Chinese salvia, species) [taxon 226208]
- **Cell lines:** Atiaa28-1 — Oryctolagus cuniculus (Rabbit), Transformed cell line (CVCL_6E94)

## Full text

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## Figures

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## References

71 references — full list in the complete paper: https://tomesphere.com/paper/PMC12935959/full.md

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Source: https://tomesphere.com/paper/PMC12935959