ArticleBMC plant biology2025
Identification of the SWEET gene family and functional characterization of PsSWEET1a and PsSWEET17b in the regulation of sugar accumulation in 'Fengtang' plum (Prunus salicina Lindl.).
Article in BMC plant biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 3 papers.
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Who cites it
3 citing papers in PubMed.
- Comparative Transcriptomic Analysis Reveals Sugar Metabolism and Accumulation Mechanisms inLife (Basel, Switzerland) · 2026Article
- Comprehensive Identification and Expression Analysis of thePlants (Basel, Switzerland) · 2025Article
- Correction: Identification of the SWEET gene family and functional characterization of PsSWEET1a and PsSWEET17b in the regulation of sugar accumulation in 'Fengtang' plum (Prunus salicina Lindl.).BMC plant biology · 2025Article
Corrections and comments
- Erratum issued
Authors and funding
4 authors.
Funding
Abstract
background'Fengtang' plum is a cultivar known for its significant sugar accumulation. Although various studies have been conducted on sugar metabolism, the specific molecular mechanisms underlying the high sugar accumulation in 'Fengtang' plum remain largely unexplored. Here, we present the role of the Sugars Will Eventually be Exported Transporters (SWEETs) family in regulating sugar accumulation in 'Fengtang' plum fruits.
resultsIn this study, 18 PsSWEET genes were identified based on homology with Arabidopsis genes and the Pfam database (ID: PF03083). Alignment of multiple sequences revealed that the seven alpha-helical transmembrane regions (7-TMs) are largely conserved in the PsSWEET family. Phylogenetic analysis demonstrated that the 18 SWEET family members could be categorized into four clades. Nine predicted motifs were identified within the PsSWEET genes of plum. The PsSWEET genes were unevenly distributed across five chromosomes, and synteny analysis revealed three pairs of fragmented duplication events. PsSWEET1a and PsSWEET17b are pivotal in 'Fengtang' plum fruit development. Subcellular localization analyses indicated that PsSWEET1a is localized to the nucleus and cytoplasm, while PsSWEET17b is associated with the vacuolar membrane. Gene function was further validated through transient silencing and overexpression of the PsSWEET1a and PsSWEET17b genes in plum fruits, which significantly impacted their soluble sugar content. Heterologous expression of PsSWEET1a and PsSWEET17b in tomato resulted in an increase in soluble sugar content due to the modulation of sugar accumulation-related genes and enzyme activities.
conclusionThe genes PsSWEET1a and PsSWEET17b, which regulate the content of soluble sugar in plum fruit, were successfully identified. This study provides a comprehensive insight into the SWEET gene family of plum, offering novel perspectives on the regulation of sugar accumulation in fruit and laying a critical foundation for further enhancement of plum fruit quality.
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