转录因子CsS40负调控TCS1的表达和咖啡因的生物合成,与茶树叶片衰老有关。

IF 7.6 Q1 GENETICS & HEREDITY
园艺研究(英文) Pub Date : 2023-08-10 eCollection Date: 2023-09-01 DOI:10.1093/hr/uhad162
Xinzhuan Yao, Hufang Chen, Antao Ai, Fen Wang, Shanshan Lian, Hu Tang, Yihe Jiang, Yujie Jiao, Yumei He, Tong Li, Litang Lu
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引用次数: 0

摘要

咖啡因被认为是流行的植物饮料茶、可可和咖啡中最重要的生物活性成分之一,但作为一种广泛分布的植物次生代谢产物,其在转录水平上的生物合成调控仍不清楚。在这里,我们报道了一种新的转录因子Camellia sinensis Senescnece 40(CsS40)作为咖啡因生物合成调节剂,它是在筛选由茶叶cDNA构建的酵母表达文库以激活茶咖啡因合成酶(TCS1)启动子时发现的。除了在酵母单杂交分析中与TCS1启动子结合并激活的非自激活CsS40克隆的多次命中外,分裂萤光素酶互补分析证明CsS40作为转录因子激活CsTCS1基因,EMSA分析也证明CsS50与TCS1基因启动子结合。一致地,免疫荧光数据表明CsS40-GFP融合定位于烟草表皮细胞的细胞核中。CsS40在‘福鼎大白’发育叶片中的表达模式与TCS1相反;CsS40在茶叶愈伤组织中的敲低和过表达分别显著增加和降低了TCS1的表达水平。CsS40的表达水平也与“福鼎大白”发育叶片和转基因愈伤组织中咖啡因的积累呈负相关。此外,CsS40的过表达减少了黄嘌呤和次黄嘌呤在烟草植株中的积累,同时增加了它们对衰老的易感性。CsS40在茶叶中的表达也受到衰老促进激素和环境因素的诱导。总之,我们发现一种新的衰老相关因子CsS40对茶品种“福鼎大白”的TCS1负调控并抑制咖啡因的积累。这项研究为茶树中一种植物特异性衰老调节剂对咖啡因生物合成的调节与叶片衰老和激素信号传导提供了新的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

The transcription factor CsS40 negatively regulates <i>TCS1</i> expression and caffeine biosynthesis in connection to leaf senescence in <i>Camellia sinensis</i>.

The transcription factor CsS40 negatively regulates <i>TCS1</i> expression and caffeine biosynthesis in connection to leaf senescence in <i>Camellia sinensis</i>.

The transcription factor CsS40 negatively regulates <i>TCS1</i> expression and caffeine biosynthesis in connection to leaf senescence in <i>Camellia sinensis</i>.

The transcription factor CsS40 negatively regulates TCS1 expression and caffeine biosynthesis in connection to leaf senescence in Camellia sinensis.

Caffeine is considered as one of the most important bioactive components in the popular plant beverages tea, cacao, and coffee, but as a wide-spread plant secondary metabolite its biosynthetic regulation at transcription level remains largely unclear. Here, we report a novel transcription factor Camellia sinensis Senescnece 40 (CsS40) as a caffeine biosynthesis regulator, which was discovered during screening a yeast expression library constructed from tea leaf cDNAs for activation of tea caffeine synthase (TCS1) promoter. Besides multiple hits of the non-self-activation CsS40 clones that bound to and activated TCS1 promoter in yeast-one-hybrid assays, a split-luciferase complementation assay demonstrated that CsS40 acts as a transcription factor to activate the CsTCS1 gene and EMSA assay also demonstrated that CsS40 bound to the TCS1 gene promoter. Consistently, immunofluorescence data indicated that CsS40-GFP fusion was localized in the nuclei of tobacco epidermal cells. The expression pattern of CsS40 in 'Fuding Dabai' developing leaves was opposite to that of TCS1; and knockdown and overexpression of CsS40 in tea leaf calli significantly increased and decreased TCS1 expression levels, respectively. The expression levels of CsS40 were also negatively correlated to caffeine accumulation in developing leaves and transgenic calli of 'Fuding Dabai'. Furthermore, overexpression of CsS40 reduced the accumulation of xanthine and hypoxanthine in tobacco plants, meanwhile, increased their susceptibility to aging. CsS40 expression in tea leaves was also induced by senescence-promoting hormones and environmental factors. Taken together, we showed that a novel senescence-related factor CsS40 negatively regulates TCS1 and represses caffeine accumulation in tea cultivar 'Fuding Dabai'. The study provides new insights into caffeine biosynthesis regulation by a plant-specific senescence regulator in tea plants in connection to leaf senescence and hormone signaling.

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