# A hierarchical abscission program regulates reproductive allocation in Prunus × yedoensis and Prunus sargentii

**Authors:** Woo-Taek Jeon, Jeong-A Kim, Ahyeon Cheon, Shawn S Y Lee, Joohyun Kang, Jung-Min Lee, Yuree Lee

PMC · DOI: 10.1093/hr/uhaf317 · Horticulture Research · 2025-11-14

## TL;DR

This study explores how cherry species use a step-by-step abscission process to control which flowers and fruits are retained for reproduction.

## Contribution

The paper reveals a hierarchical abscission program in cherry species that acts as a reproductive filter to optimize fruit production.

## Key findings

- Abscission zones in Prunus species are either pre-formed or formed de novo, depending on the organ.
- Ethylene responsiveness and reactive oxygen species drive abscission zone activation and cell differentiation.
- Species-specific abscission strategies influence pollination and fertilization outcomes.

## Abstract

Organ abscission is essential for optimal reproduction, yet its regulation in perennial woody plant species is poorly understood. To investigate how abscission is spatially and temporally regulated during reproduction, we analyzed five sequential abscission events in the cherry species Prunus × yedoensis (Cerasus × yedoensis, Somei-Yoshino) and Prunus sargentii var. verecunda (Bunhong-Beot): abscission of the petals, calyces, flower pedicels, fruit pedicels, and peduncles. The abscission zone of the calyx formed de novo upon activation, whereas other abscission zones were pre-formed but developmentally arrested. Localized ethylene responsiveness reactivated these zones, promoting cell division, differentiation of residuum and secession cells on either side of the abscission zone, and lignin deposition in some cases. This progression was accompanied by reactive oxygen species accumulation and pH shifts. We observed species-specific differences during early floral abscission: P. yedoensis shed petals rapidly in a pollination-independent manner, whereas P. sargentii retained petals on unpollinated flowers, which later abscised with the pedicel, potentially extending the fertilization window. Both species employed a post-fertilization developmental gate via fruit pedicel abscission to selectively eliminate small, slow-growing fruits. These findings reveal that Prunus species coordinate a hierarchical abscission program functioning as a multilayered reproductive filter, progressively refining investment decisions to determine the final fruit set.

## Linked entities

- **Chemicals:** ethylene (PubChem CID 6325), lignin (PubChem CID 175586)
- **Species:** Prunus yedoensis (taxon 3759), Prunus sargentii var. verecunda (taxon 2854737)

## Full-text entities

- **Genes:** IDA (Putative membrane lipoprotein) [NCBI Gene 843208] {aka INFLORESCENCE DEFICIENT IN ABSCISSION}
- **Diseases:** DEFICIENT (MESH:D007153), ACC (MESH:C538385)
- **Chemicals:** superoxide (MESH:D013481), BCECF (-), Hydrogen peroxide (MESH:D006861), glycerol (MESH:D005990), sodium phosphate (MESH:C018279), zeolite (MESH:D017641), lignin (MESH:D008031), cytokinin (MESH:D003583), sucrose (MESH:D013395), perlite (MESH:C003076), KOH (MESH:C029943), glutaraldehyde (MESH:D005976), 3,3'-diaminobenzidine (MESH:D015100), Tween-20 (MESH:D011136), DAB (MESH:C000469), DMSO (MESH:D004121), Auxin (MESH:D007210), ROS (MESH:D017382), metal (MESH:D008670), platinum (MESH:D010984), ABA (MESH:D000040), lanolin (MESH:D007809), vermiculite (MESH:C003760), granite (MESH:C007886), osmium tetroxide (MESH:D009993), Ethylene (MESH:C036216), lactic acid (MESH:D019344), phloroglucinol (MESH:D010696), agar (MESH:D000362), Triton X-100 (MESH:D017830), chlorophylls (MESH:D002734), carbon (MESH:D002244), water (MESH:D014867), 2-(N-morpholino) ethanesulfonic acid (MESH:C004550), HCl (MESH:D006851), ethanol (MESH:D000431), 1-Aminocyclopropane-1-carboxylate (MESH:C023863), Toluidine blue (MESH:D014048), polyethylene (MESH:D020959)
- **Species:** Solanum lycopersicum (tomato, species) [taxon 4081], Brassica napus (oilseed rape, species) [taxon 3708], Arabidopsis thaliana (mouse-ear cress, species) [taxon 3702], Capsicum annuum (sweet pepper, species) [taxon 4072], Prunus avium (gean, species) [taxon 42229], Litchi chinensis (litchi, species) [taxon 151069], Homo sapiens (human, species) [taxon 9606], Oryza sativa (Asian cultivated rice, species) [taxon 4530], Brachypodium distachyon (annual false brome, species) [taxon 15368], Prunus (genus) [taxon 3754], Prunus persica (peach, species) [taxon 3760], Malus domestica (apple, species) [taxon 3750], Prunus yedoensis (Potomac cherry, species) [taxon 3759], Sparganophilus sp. L (species) [taxon 1046293], Pyrus communis (pear, species) [taxon 23211], Prunus armeniaca (apricot, species) [taxon 36596], Prunus sargentii (species) [taxon 97308], Citrus (genus) [taxon 2706], Mangifera indica (mango, species) [taxon 29780], Prunus dulcis (almond, species) [taxon 3755]
- **Mutations:** C-22 C, glycine (G) instead of alanine (A), ACC at 5

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12946680/full.md

## References

88 references — full list in the complete paper: https://tomesphere.com/paper/PMC12946680/full.md

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Source: https://tomesphere.com/paper/PMC12946680