The <i>CsMYB36-CsSWEET17</i> module mediates the calcium-induced sucrose accumulation in citrus

Sugar content serves as a crucial determinant of fruit flavor quality and nutritional value. Calcium plays extensive regulatory roles in fruit development and quality formation, yet the molecular mechanisms underlying calcium-mediated sugar accumulation remain poorly understood. In this study, we demonstrate that calcium treatment enhances sugar accumulation in both citrus fruits and calli, concomitant with upregulated expression of the sucrose transporter gene <i>CsSWEET17</i>. Functional characterization revealed that the membrane-localized CsSWEET17 protein exhibits sucrose transport activity. Transgenic overexpression of <i>CsSWEET17</i> in citrus juice sacs, calli and heterologous tomato systems consistently elevated sucrose levels. Conversely, suppression of <i>CsSWEET17</i> expression through either virus-induced gene silencing or RNA interference significantly reduced sucrose content in citrus. Further investigation identified CsMYB36 as a calcium-responsive transcription factor that directly activates <i>CsSWEET17</i> expression. Transgenic validation demonstrated that both calcium signaling and CsMYB36-mediated sucrose accumulation strictly depend on <i>CsSWEET17</i> transcriptional regulation. Our findings elucidate a novel calcium-MYB36-SWEET17 regulatory module controlling sucrose accumulation, providing molecular insights into calcium-based strategies in citrus quality improvement and informing fundamental mechanisms of sugar transporter regulation in fruit crops.

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Publication Details

Journal
Horticulture Research
Published
2025-07-16
DOI
https://doi.org/10.1093/hr/uhaf175
Citations
1
Primary Topic
Plant nutrient uptake and metabolism
Type
article
Field-Weighted Citation Impact
1.75

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article

The CsMYB36-CsSWEET17 module mediates the calcium-induced sucrose accumulation in citrus

Xijing Sheng, Manqiao Li, Zuolin Mao, Yangzhi Luo et al.
1 citations
Horticulture Research
Plant nutrient uptake and metabolism
1.75
article

The CsMYB36-CsSWEET17 module mediates the calcium-induced sucrose accumulation in citrus

Xijing Sheng, Manqiao Li, Zuolin Mao, Yangzhi Luo, Ji‐Hong Liu, Chunlong Li, Xiawan Zhai
article en
1 citations

Abstract

Sugar content serves as a crucial determinant of fruit flavor quality and nutritional value. Calcium plays extensive regulatory roles in fruit development and quality formation, yet the molecular mechanisms underlying calcium-mediated sugar accumulation remain poorly understood. In this study, we demonstrate that calcium treatment enhances sugar accumulation in both citrus fruits and calli, concomitant with upregulated expression of the sucrose transporter gene <i>CsSWEET17</i>. Functional characterization revealed that the membrane-localized CsSWEET17 protein exhibits sucrose transport activity. Transgenic overexpression of <i>CsSWEET17</i> in citrus juice sacs, calli and heterologous tomato systems consistently elevated sucrose levels. Conversely, suppression of <i>CsSWEET17</i> expression through either virus-induced gene silencing or RNA interference significantly reduced sucrose content in citrus. Further investigation identified CsMYB36 as a calcium-responsive transcription factor that directly activates <i>CsSWEET17</i> expression. Transgenic validation demonstrated that both calcium signaling and CsMYB36-mediated sucrose accumulation strictly depend on <i>CsSWEET17</i> transcriptional regulation. Our findings elucidate a novel calcium-MYB36-SWEET17 regulatory module controlling sucrose accumulation, providing molecular insights into calcium-based strategies in citrus quality improvement and informing fundamental mechanisms of sugar transporter regulation in fruit crops.

Horticulture ResearchVol. 12(10)
Huazhong Agricultural University (CN), Shanghai Zhangjiang Laboratory (CN)
National Natural Science Foundation of China, Huazhong Agricultural University, National Key Research and Development Program of China, Fundamental Research Funds for the Central Universities
Openalex Percentile: Top 14%
Plant nutrient uptake and metabolism
1.75
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