近日，華中農業大學果蔬園藝作物種質創新與利用全國重點實驗室、湖北洪山實驗室、園藝林學學院李春龍教授課題組在Journal of Integrative Plant Biology上發表了題為“The CBL1/CIPK23 phosphorylates tonoplast sugar transporter TST2 to enhance the sugar accumulation in sweet orange （Citrus sinensis）”的研究論文，揭示了CBL1/CIPK23-TST2模塊響應鈣信號通過調控液泡膜糖轉運蛋白活性作用于柑橘果實糖積累的機制。
柑橘是我國及全球產量最高的水果，其風味和營養價值備受消費者青睞。其中果實甜度是影響消費者喜好和選擇的重要因素?？扇苄蕴侵饕e累于果實液泡中，這一過程依賴于液泡膜定位的糖轉運蛋白，但目前關于柑橘果實糖分累積的具體機制尚未完全了解。
為了深入理解柑橘果實風味品質的形成以及調控機理，該研究在課題組前期柑橘果實液泡蛋白組的基礎上，發掘到與可溶性糖積累顯著正相關的液泡膜轉運蛋白CsTST2。利用酵母和爪蟾蛙卵體系證明CsTST2具有轉運己糖和雙糖的功能。通過柑橘汁胞瞬時轉化、柑橘愈傷組織及番茄材料穩定遺傳轉化，證明過表達CsTST2可以顯著提高轉基因材料中糖含量，而干涉表達則降低糖含量。
通過酵母雙雜交文庫篩選，鑒定到與CsTST2互作的蛋白CsCIPK23。體外和體內實驗證實CsCIPK23與CsTST2非跨膜LOOP環互作，并且磷酸化Ser277/337/354位點，以上位點突變為非磷酸化狀態后降低CsTST2的糖轉運活性。進一步分析表明CsCIPK23與CsCBL1互作響應鈣信號，并且CsCIPK23及鈣處理增加可溶性糖積累，這一過程依賴于CsTST2的存在及其磷酸化修飾水平。
綜上，本研究證實了CsTST2貢獻于柑橘果實液泡中可溶性糖的轉運積累，而CsCIPK23通過與鈣信號傳感器CsCBL1形成復合物，磷酸化修飾CsTST2以增強其轉運活性，進一步促進柑橘果實糖分的積累（圖2）。這項研究不僅揭示了CsTST2在柑橘果實糖積累中的重要作用，還為鈣信號調控果實風味品質形成的分子機制提供新的見解。
華中農業大學園藝林學學院李春龍和劉繼紅教授為共同通訊作者，2022級果樹學博士研究生李夢迪為該論文的第一作者。該研究依托華中農業大學果蔬園藝作物種質創新與利用全國重點實驗室平臺，獲得國家重點研發計劃項目、國家自然科學基金項目等項目資助。
【英文摘要】
Fruit taste quality is greatly influenced by the content of soluble sugars, which are predominantly stored in the vacuolar lumen. However, the accumulation and regulation mechanisms of sugars in most fruits remain unclear. Recently, we established the citrus fruit vacuole proteome and discovered the major transporters localized in the vacuole membrane. Here, we demonstrated that the expression of tonoplast sugar transporter 2 （CsTST2） is closely associated with sugar accumulation during sweet orange （Citrus sinensis） ripening. It was further demonstrated that CsTST2 had the function of transporting hexose and sucrose into the vacuole. Overexpression of CsTST2 resulted in an elevation of sugar content in citrus juice sac, calli, and tomato fruit, whereas the downregulation of its expression led to the reduction in sugar levels. CsTST2 was identified as interacting with CsCIPK23, which binds to the upstream calcium signal sensor protein CsCBL1. The phosphorylation of the three serine residues （Ser277, Ser337, and Ser354） in the loop region of CsTST2 by CsCIPK23 is crucial for maintaining the sugar transport activity of CsTST2. Additionally, the expression of CsCIPK23 is positively correlated with sugar content. Genetic evidence further confirmed that calcium and CsCIPK23‐mediated increase in sugar accumulation depends on CsTST2 and its phosphorylation level. These findings not only unveil the functional mechanism of CsTST2 in sugar accumulation, but also explore a vital calcium signal regulation module of CsCBL1/CIPK23 for citrus sweetness quality.
日期：2025-02-03
柑橘是我國及全球產量最高的水果，其風味和營養價值備受消費者青睞。其中果實甜度是影響消費者喜好和選擇的重要因素?？扇苄蕴侵饕e累于果實液泡中，這一過程依賴于液泡膜定位的糖轉運蛋白，但目前關于柑橘果實糖分累積的具體機制尚未完全了解。
為了深入理解柑橘果實風味品質的形成以及調控機理，該研究在課題組前期柑橘果實液泡蛋白組的基礎上，發掘到與可溶性糖積累顯著正相關的液泡膜轉運蛋白CsTST2。利用酵母和爪蟾蛙卵體系證明CsTST2具有轉運己糖和雙糖的功能。通過柑橘汁胞瞬時轉化、柑橘愈傷組織及番茄材料穩定遺傳轉化，證明過表達CsTST2可以顯著提高轉基因材料中糖含量，而干涉表達則降低糖含量。
通過酵母雙雜交文庫篩選，鑒定到與CsTST2互作的蛋白CsCIPK23。體外和體內實驗證實CsCIPK23與CsTST2非跨膜LOOP環互作，并且磷酸化Ser277/337/354位點，以上位點突變為非磷酸化狀態后降低CsTST2的糖轉運活性。進一步分析表明CsCIPK23與CsCBL1互作響應鈣信號，并且CsCIPK23及鈣處理增加可溶性糖積累，這一過程依賴于CsTST2的存在及其磷酸化修飾水平。
綜上，本研究證實了CsTST2貢獻于柑橘果實液泡中可溶性糖的轉運積累，而CsCIPK23通過與鈣信號傳感器CsCBL1形成復合物，磷酸化修飾CsTST2以增強其轉運活性，進一步促進柑橘果實糖分的積累（圖2）。這項研究不僅揭示了CsTST2在柑橘果實糖積累中的重要作用，還為鈣信號調控果實風味品質形成的分子機制提供新的見解。
華中農業大學園藝林學學院李春龍和劉繼紅教授為共同通訊作者，2022級果樹學博士研究生李夢迪為該論文的第一作者。該研究依托華中農業大學果蔬園藝作物種質創新與利用全國重點實驗室平臺，獲得國家重點研發計劃項目、國家自然科學基金項目等項目資助。
【英文摘要】
Fruit taste quality is greatly influenced by the content of soluble sugars, which are predominantly stored in the vacuolar lumen. However, the accumulation and regulation mechanisms of sugars in most fruits remain unclear. Recently, we established the citrus fruit vacuole proteome and discovered the major transporters localized in the vacuole membrane. Here, we demonstrated that the expression of tonoplast sugar transporter 2 （CsTST2） is closely associated with sugar accumulation during sweet orange （Citrus sinensis） ripening. It was further demonstrated that CsTST2 had the function of transporting hexose and sucrose into the vacuole. Overexpression of CsTST2 resulted in an elevation of sugar content in citrus juice sac, calli, and tomato fruit, whereas the downregulation of its expression led to the reduction in sugar levels. CsTST2 was identified as interacting with CsCIPK23, which binds to the upstream calcium signal sensor protein CsCBL1. The phosphorylation of the three serine residues （Ser277, Ser337, and Ser354） in the loop region of CsTST2 by CsCIPK23 is crucial for maintaining the sugar transport activity of CsTST2. Additionally, the expression of CsCIPK23 is positively correlated with sugar content. Genetic evidence further confirmed that calcium and CsCIPK23‐mediated increase in sugar accumulation depends on CsTST2 and its phosphorylation level. These findings not only unveil the functional mechanism of CsTST2 in sugar accumulation, but also explore a vital calcium signal regulation module of CsCBL1/CIPK23 for citrus sweetness quality.
日期：2025-02-03
