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两个 Dof 转录因子通过激活 C-葡萄糖基转移酶促进金桔果实中类黄酮的合成。

Two Dof transcription factors promote flavonoid synthesis in kumquat fruit by activating C-glucosyltransferase.

机构信息

College of Horticulture and Landscape Architecture, Southwest University, Chongqing 400715, China; Key Laboratory of Horticulture Science for Southern Mountainous Regions, Ministry of Education, Chongqing 400715, China.

College of Horticulture and Landscape Architecture, Southwest University, Chongqing 400715, China.

出版信息

Plant Sci. 2022 May;318:111234. doi: 10.1016/j.plantsci.2022.111234. Epub 2022 Feb 23.

Abstract

Although DNA binding with one finger (Dof) constitutes a crucial plant-specific family of transcription factors (TFs) that plays important roles in a wide range of biological processes, the molecular mechanisms underlying Dof regulation of flavonoid biosynthesis in plants remain largely unknown. Here, we characterized 28 Dof genes (FhDof1-FhDof28) from the 'Hongkong' kumquat (Fortunella hindsii) cultivar genome. Promoter analysis and transcriptome profiling revealed that four FhDofs - FhDof4, FhDof9, FhDof15, and FhDof16 - may be involved in flavonoid biosynthesis through binding to the flavonoid C-glycosyltransferase (FhCGT) promoter. We cloned homologous genes of four FhDofs, designated as FcDof4, FcDof9, FcDof15, FcDof16, and a homologous gene of FhCGT, designated as FcCGT, from the widely cultivated 'HuaPi' kumquat (F. crassifolia). Quantitative reverse transcription-polymerase chain reaction analysis revealed that FcDof4 and FcDof16 were significantly correlated with FcCGT expression during development stages in the 'HuaPi' fruit (Pearson's correlation coefficient > 0.7) and were localized to the nucleus. Results of yeast one-hybrid, electrophoretic mobility shift, and dual-luciferase assays indicated that the two FcDofs trigger FcCGT expression by specifically binding to its promoters. Moreover, transient overexpression of FcDof4 and FcDof16 enhances the transcription of structural genes in the flavonoid biosynthetic pathway and increases C-glycosylflavonoid content. Our results provide strong evidence that the TFs FcDof4 and FcDof16 promote flavonoid synthesis in kumquat fruit by activating FcCGT expression.

摘要

尽管 DNA 结合一个手指 (Dof) 构成了一个关键的植物特异性转录因子 (TFs) 家族,在广泛的生物学过程中发挥着重要作用,但 Dof 调节植物类黄酮生物合成的分子机制在很大程度上仍然未知。在这里,我们从 'Hongkong' 金桔 ( Fortunella hindsii ) 品种基因组中鉴定了 28 个 Dof 基因 (FhDof1-FhDof28)。启动子分析和转录组分析表明,四个 FhDofs - FhDof4、FhDof9、FhDof15 和 FhDof16 - 可能通过与类黄酮 C-糖基转移酶 (FhCGT) 启动子结合而参与类黄酮生物合成。我们从广泛种植的 'HuaPi' 金桔 ( F. crassifolia ) 中克隆了四个 FhDofs 的同源基因,分别命名为 FcDof4、FcDof9、FcDof15 和 FcDof16,以及 FhCGT 的同源基因,命名为 FcCGT。定量反转录聚合酶链反应分析显示,在 'HuaPi' 果实发育阶段,FcDof4 和 FcDof16 与 FcCGT 表达呈显著相关 (皮尔逊相关系数 > 0.7),并定位于细胞核内。酵母单杂交、电泳迁移率变动分析和双荧光素酶报告基因分析结果表明,这两个 FcDofs 通过特异性结合其启动子触发 FcCGT 表达。此外,瞬时过表达 FcDof4 和 FcDof16 增强了类黄酮生物合成途径中结构基因的转录,并增加了 C-糖基黄酮的含量。我们的研究结果提供了有力的证据表明,TFs FcDof4 和 FcDof16 通过激活 FcCGT 的表达促进金桔果实中类黄酮的合成。

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