Key Laboratory of South China Agricultural Plant Molecular Analysis and Genetic Improvement, South China Botanical Garden, Chinese Academy of Sciences, Guangzhou, China 510650.
Department of Plant and Soil Sciences and Kentucky Tobacco Research and Development Center, University of Kentucky, Lexington, Kentucky 40546.
Plant Physiol. 2019 Jul;180(3):1336-1350. doi: 10.1104/pp.19.00489. Epub 2019 May 13.
is the exclusive source of an array of terpenoid indole alkaloids including the anticancer drugs vincristine and vinblastine, derived from the coupling of catharanthine and vindoline. Leaf-synthesized vindoline is regulated by light. A seven-step enzymatic process is involved in the sequential conversion of tabersonine to vindoline; however, the regulatory mechanism controlling the expression of genes encoding these enzymes has not been elucidated. Here, we identified CrGATA1, an Leu-Leu-Met domain GATA transcription factor that regulates light-induced vindoline biosynthesis in seedlings. Expression of and the vindoline pathway genes , , , , and was significantly induced by light. In addition, CrGATA1 activated the promoters of five light-responsive vindoline pathway genes in plant cells. Two GATC motifs in the promoter were critical for CrGATA1-mediated transactivation. Transient overexpression of in seedlings resulted in up-regulation of vindoline pathway genes and increased vindoline accumulation. Conversely, virus-induced gene silencing of in young leaves significantly repressed key vindoline pathway genes and reduced vindoline accumulation. Furthermore, we showed that a Phytochrome Interacting Factor, CrPIF1, is a repressor of and vindoline biosynthesis. Transient overexpression or virus-induced gene silencing of in seedlings altered and vindoline pathway gene expression in the dark. CrPIF1 repressed and promoter activity by binding to G/E-box/PBE elements. Our findings reveal a regulatory module involving Phytochrome Interacting Factor -GATA that governs light-mediated biosynthesis of specialized metabolites.
是一系列萜吲哚生物碱的唯一来源,包括抗癌药物长春新碱和长春碱,这些生物碱来源于卡他林和长春碱的偶联。叶合成的长春碱受光照调控。从三亚藤碱到长春碱的连续转化涉及七个酶促步骤;然而,控制编码这些酶的基因表达的调控机制尚未阐明。在这里,我们鉴定了 CrGATA1,一种 Leu-Leu-Met 结构域 GATA 转录因子,它调节 幼苗中光诱导的长春碱生物合成。表达和长春碱途径基因 、 、 、 和 被光照显著诱导。此外,CrGATA1 在植物细胞中激活了五个光响应长春碱途径基因的启动子。 启动子中的两个 GATC 基序对于 CrGATA1 介导的转录激活至关重要。在 幼苗中转瞬表达 导致长春碱途径基因上调和长春碱积累增加。相反,在年轻的 叶片中病毒诱导的基因沉默显著抑制了关键的长春碱途径基因并减少了长春碱的积累。此外,我们表明,一个 Phytochrome Interacting Factor,CrPIF1,是 和长春碱生物合成的抑制剂。在 幼苗中转瞬表达或病毒诱导的基因沉默改变了 和黑暗中长春碱途径基因的表达。CrPIF1 通过结合 G/E-box/PBE 元件抑制 和 启动子活性。我们的研究结果揭示了一个涉及 Phytochrome Interacting Factor-GATA 的调控模块,它控制着特殊代谢物的光介导生物合成。