Sugar signaling-mediated hormonal regulatory networks: molecular mechanisms underlying fruit abscission and development in seedless litchi

Seedless litchi (Litchi chinensis ‘Wu He’) exhibits an excellent parthenocarpic trait, the physiological regulation of which during early fruit development is critical for ultimate yield. Sugar availability serves as the predominant factor governing both fruit abscission and development. However, the molecular mechanisms by which sugar signaling mediates hormonal networks to regulate these processes in seedless litchi remain unclear. This study explored the regulatory patterns in seedless litchi during the massive abscission stage (MA stage) and subsequent developmental stages (SD stages), through integrated physiological and transcriptomic analyses. At the MA stage (15 days after flowering, 15 DAF), the concentrations of glucose and fructose in fruits dropped to their lowest levels. Concurrently, auxin and abscisic acid (ABA) levels increased significantly, while the ethylene (ET) precursor (1-aminocyclopropane-1-carboxylic acid, ACC) content declined. Tissue section revealed that both cell size and cell number were at their lowest, indicating delayed fruit development. Upon entering the SD stages (22 DAF, 29 DAF, 36 DAF), fruit abscission progressively decreased as sugar availability improved. During these stages, cytokinin (iP-type-CK) and gibberellin (GA3) levels increased, accompanied by synchronized increases in cell volume and number, leading to continuous fruit enlargement. Transcriptomic analysis demonstrated that differentially expressed genes were primarily enriched in pathways related to starch and sucrose metabolism, hormone metabolism and signal transduction. During the MA stage, expression of genes such as MAT, ACS, ACO, CTR1, ZEP,NCED, PP2C, and SnRK2 was upregulated, whereas EIN2 was downregulated. In contrast, the SD stages exhibited upregulation of IPT,B-ARR, KAO, GID1, GID2, TFs and DELLA genes, alongside downregulation of CKX, A-ARR, and GA2ox. These gene expression patterns were consistent with fluctuations in hormone levels and collectively regulated fruit abscission and development. RT-qPCR validation confirmed the accuracy of the RNA-Seq results. Deficiencies in fructose and glucose mediate ABA and ET accumulation while disrupting polar auxin transport, thereby exacerbating fruit abscission. Following massive fruit abscission, improved sugar availability enhanced the effects of CK and GA, which promoted cell division and expansion, resulting in gradual fruit enlargement. These findings elucidate the sugar signaling-mediated hormonal regulatory networks during seedless litchi abscission and development, providing a theoretical foundation for achieving high and stable yields in orchards.

Authors

Institutions

Publication Details

Journal
BMC Plant Biology
Published
2025-11-10
DOI
https://doi.org/10.1186/s12870-025-07557-9
Primary Topic
Plant Molecular Biology Research
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Sugar signaling-mediated hormonal regulatory networks: molecular mechanisms underlying fruit abscission and development in seedless litchi

Songgang Li, Haoting Shi, Qingmei Hong, Fang Li et al.
BMC Plant Biology
Plant Molecular Biology Research
article

Sugar signaling-mediated hormonal regulatory networks: molecular mechanisms underlying fruit abscission and development in seedless litchi

Songgang Li, Haoting Shi, Qingmei Hong, Fang Li, Jiabao Wang, Kun‐Kun Zhao, Xiao Zhang, Huanling Li, Zhaoyin Gao
article en

Abstract

Seedless litchi (Litchi chinensis ‘Wu He’) exhibits an excellent parthenocarpic trait, the physiological regulation of which during early fruit development is critical for ultimate yield. Sugar availability serves as the predominant factor governing both fruit abscission and development. However, the molecular mechanisms by which sugar signaling mediates hormonal networks to regulate these processes in seedless litchi remain unclear. This study explored the regulatory patterns in seedless litchi during the massive abscission stage (MA stage) and subsequent developmental stages (SD stages), through integrated physiological and transcriptomic analyses. At the MA stage (15 days after flowering, 15 DAF), the concentrations of glucose and fructose in fruits dropped to their lowest levels. Concurrently, auxin and abscisic acid (ABA) levels increased significantly, while the ethylene (ET) precursor (1-aminocyclopropane-1-carboxylic acid, ACC) content declined. Tissue section revealed that both cell size and cell number were at their lowest, indicating delayed fruit development. Upon entering the SD stages (22 DAF, 29 DAF, 36 DAF), fruit abscission progressively decreased as sugar availability improved. During these stages, cytokinin (iP-type-CK) and gibberellin (GA3) levels increased, accompanied by synchronized increases in cell volume and number, leading to continuous fruit enlargement. Transcriptomic analysis demonstrated that differentially expressed genes were primarily enriched in pathways related to starch and sucrose metabolism, hormone metabolism and signal transduction. During the MA stage, expression of genes such as MAT, ACS, ACO, CTR1, ZEP,NCED, PP2C, and SnRK2 was upregulated, whereas EIN2 was downregulated. In contrast, the SD stages exhibited upregulation of IPT,B-ARR, KAO, GID1, GID2, TFs and DELLA genes, alongside downregulation of CKX, A-ARR, and GA2ox. These gene expression patterns were consistent with fluctuations in hormone levels and collectively regulated fruit abscission and development. RT-qPCR validation confirmed the accuracy of the RNA-Seq results. Deficiencies in fructose and glucose mediate ABA and ET accumulation while disrupting polar auxin transport, thereby exacerbating fruit abscission. Following massive fruit abscission, improved sugar availability enhanced the effects of CK and GA, which promoted cell division and expansion, resulting in gradual fruit enlargement. These findings elucidate the sugar signaling-mediated hormonal regulatory networks during seedless litchi abscission and development, providing a theoretical foundation for achieving high and stable yields in orchards.

BMC Plant BiologyVol. 25(1)
Chinese Academy of Tropical Agricultural Sciences (CN), Environment and Plant Protection Research Institute (CN), Ministry of Agriculture (EE), Tropical Crops Genetic Resources Institute (CN)
Openalex Percentile: Top 75%
Plant Molecular Biology Research
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.