首页> 外文期刊>Frontiers in Plant Science >DNA Methylation Influences Chlorogenic Acid Biosynthesis in Lonicera japonica by Mediating LjbZIP8 to Regulate Phenylalanine Ammonia-Lyase 2 Expression
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DNA Methylation Influences Chlorogenic Acid Biosynthesis in Lonicera japonica by Mediating LjbZIP8 to Regulate Phenylalanine Ammonia-Lyase 2 Expression

机译:DNA甲基化介导LjbZIP8调节苯丙氨酸氨解酶2的表达影响<忍冬>忍冬的绿原酸生物合成

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The content of active compounds differ in buds and flowers of Lonicera japonica (FLJ) and L. japonica var. chinensis (rFLJ). Chlorogenic acid (CGAs) were major active compounds of L. japonica and regarded as measurements for quality evaluation. However, little is known concerning the formation of active compounds at the molecular level. We quantified the major CGAs in FLJ and rFLJ, and found the concentrations of CGAs were higher in the buds of rFLJ than those of FLJ. Further analysis of CpG methylation of CGAs biosynthesis genes showed differences between FLJ and rFLJ in the 5′-UTR of phenylalanine ammonia-lyase 2 ( PAL2 ). We identified 11 LjbZIP proteins and 24 rLjbZIP proteins with conserved basic leucine zipper domains, subcellular localization, and electrophoretic mobility shift assay showed that the transcription factor LjbZIP8 is a nuclear-localized protein that specifically binds to the G-box element of the LjPAL2 5′-UTR. Additionally, a transactivation assay and LjbZIP8 overexpression in transgenic tobacco indicated that LjbZIP8 could function as a repressor of transcription. Finally, treatment with 5-azacytidine decreased the transcription level of LjPAL2 and CGAs content in FLJ leaves. These results raise the possibility that DNA methylation might influence the recruitment of LjbZIP8, regulating PAL2 expression level and CGAs content in L. japonica .
机译:忍冬(Lonicera japonica)和日本忍冬(L. japonica var)的芽和花中活性化合物的含量不同。中华(rFLJ)。绿原酸(CGAs)是粳稻的主要活性成分,被认为是质量评价的标准。但是,关于在分子水平上形成活性化合物的知之甚少。我们对FLJ和rFLJ中的主要CGA进行了定量,发现rFLJ的芽中CGA的浓度高于FLJ。对CGAs生物合成基因的CpG甲基化的进一步分析表明,在苯丙氨酸解氨酶2(PAL2)的5'-UTR中,FLJ和rFLJ之间存在差异。我们鉴定了11个LjbZIP蛋白和24个rLjbZIP蛋白,它们具有保守的基本亮氨酸拉链结构域,亚细胞定位和电泳迁移率变动分析,表明转录因子LjbZIP8是一种核定域蛋白,与LjPAL2 5'的G-box元件特异性结合。 -UTR。此外,反式激活试验和LjbZIP8在转基因烟草中的过表达表明LjbZIP8可以作为转录的阻遏物。最后,用5-氮杂胞苷处理降低了FLJ叶片中LjPAL2的转录水平和CGA含量。这些结果增加了DNA甲基化可能影响LjbZIP8募集,调节L.japonica中PAL2表达水平和CGA含量的可能性。

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