Comprehensive Identification and Expression Analysis of the SWEET Gene Family in Actinidia eriantha Reveals That Two AeSWEET11 Genes Function in Sucrose and Hexose Transport

Sugars are key metabolites influencing the flavor and quality of kiwifruit, with their accumulation in fruit relying on sugar transporters. Recently identified sugar transporters known as SWEETs play significant roles in modulating plant growth, development, and fruit ripening. However, the characteristics of <i>SWEET</i> genes in <i>Actinidia eriantha</i> remain poorly understood. In this study, a total of 26 <i>AeSWEET</i> genes were identified across 17 chromosomes. These genes encoded proteins ranging from 198 to 305 amino acids in length and contained 5 to 7 transmembrane helices. Both interspecific and intraspecific phylogenetic trees categorized AeSWEET proteins into four distinct clades. The motif and domain structures were conserved within each clade, although variations were observed in exon-intron organizations. One tandem and fourteen segmental duplication events were identified as primary drivers of the <i>AeSWEET</i> family expansion. Comparative syntenic mapping showed a closer homology of the <i>AeSWEET</i> family with that of dicotyledons compared to monocotyledons. Promoter <i>cis</i>-element analysis indicated the potential responses of <i>AeSWEET</i> genes to five phytohormones and seven environmental stressors. Quantitative real-time PCR analysis revealed tissue-specific expression profiles of <i>AeSWEET</i> genes, with two <i>AeSWEET11</i> genes (<i>AeSWEET11a</i> and <i>AeSWEET11b</i>) showing significantly higher expression levels in fruit tissues. Their expressions were positively correlated with sucrose, fructose, and glucose contents throughout fruit development and ripening. Transient transformation tests in tobacco leaves verified the predominant localization of AeSWEET11a and AeSWEET11b to the plasma membrane. Functional assays in yeast mutants revealed that AeSWEET11a and AeSWEET11b both possessed sucrose and hexose transport activities. These findings highlight the potential of targeting <i>AeSWEET11a</i> and <i>AeSWEET11b</i> to enhance sugar accumulation in the fruit of <i>A. eriantha</i>, thereby providing a foundation for improving the flavor profile of commercial cultivars.

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Plants
Published
2025-10-11
DOI
https://doi.org/10.3390/plants14203140
Primary Topic
Plant nutrient uptake and metabolism
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article
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article

Comprehensive Identification and Expression Analysis of the SWEET Gene Family in Actinidia eriantha Reveals That Two AeSWEET11 Genes Function in Sucrose and Hexose Transport

Qingqing Huang, Minxia Gao, Yiting Chen, Ruilian Lai et al.
Plants
Plant nutrient uptake and metabolism
article

Comprehensive Identification and Expression Analysis of the SWEET Gene Family in Actinidia eriantha Reveals That Two AeSWEET11 Genes Function in Sucrose and Hexose Transport

Qingqing Huang, Minxia Gao, Yiting Chen, Ruilian Lai, Xin Feng
article en

Abstract

Sugars are key metabolites influencing the flavor and quality of kiwifruit, with their accumulation in fruit relying on sugar transporters. Recently identified sugar transporters known as SWEETs play significant roles in modulating plant growth, development, and fruit ripening. However, the characteristics of <i>SWEET</i> genes in <i>Actinidia eriantha</i> remain poorly understood. In this study, a total of 26 <i>AeSWEET</i> genes were identified across 17 chromosomes. These genes encoded proteins ranging from 198 to 305 amino acids in length and contained 5 to 7 transmembrane helices. Both interspecific and intraspecific phylogenetic trees categorized AeSWEET proteins into four distinct clades. The motif and domain structures were conserved within each clade, although variations were observed in exon-intron organizations. One tandem and fourteen segmental duplication events were identified as primary drivers of the <i>AeSWEET</i> family expansion. Comparative syntenic mapping showed a closer homology of the <i>AeSWEET</i> family with that of dicotyledons compared to monocotyledons. Promoter <i>cis</i>-element analysis indicated the potential responses of <i>AeSWEET</i> genes to five phytohormones and seven environmental stressors. Quantitative real-time PCR analysis revealed tissue-specific expression profiles of <i>AeSWEET</i> genes, with two <i>AeSWEET11</i> genes (<i>AeSWEET11a</i> and <i>AeSWEET11b</i>) showing significantly higher expression levels in fruit tissues. Their expressions were positively correlated with sucrose, fructose, and glucose contents throughout fruit development and ripening. Transient transformation tests in tobacco leaves verified the predominant localization of AeSWEET11a and AeSWEET11b to the plasma membrane. Functional assays in yeast mutants revealed that AeSWEET11a and AeSWEET11b both possessed sucrose and hexose transport activities. These findings highlight the potential of targeting <i>AeSWEET11a</i> and <i>AeSWEET11b</i> to enhance sugar accumulation in the fruit of <i>A. eriantha</i>, thereby providing a foundation for improving the flavor profile of commercial cultivars.

PlantsVol. 14(20)
Fujian Academy of Agricultural Sciences (CN), Fruit Research Institute (CN)
Openalex Percentile: Top 79%
Plant nutrient uptake and metabolism
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