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Regulation of anthocyanin biosynthesis by nitrogen in TTG1–GL3/TT8–PAP1-programmed red cells of Arabidopsis thaliana

机译:拟南芥TTG1-GL3 / TT8-PAP1程序化红细胞中氮对花色苷生物合成的调控

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Nitrogen nutrients can regulate anthocyanin biosynthesis in Arabidopsis thaliana. In this investigation, we report the nitrogen regulation of anthocyanin biosynthesis activated by TTG1–GL3/TT8–PAP1 in red pap1-D cells. To understand the mechanisms of nitrogen regulation, we employed red pap1-D cells and wild-type cells (as a control) to examine the effects of different nitrogen treatments on anthocyanin biosynthesis. In general, the higher concentrations of ammonium and high total nitrogen tested (e.g., 58.8 and 29.8 mM total nitrogen consisting of NH4NO3 and KNO3) reduced the levels and molecular diversity of anthocyanins; in contrast, the lower concentrations of ammonium and total nitrogen conditions (e.g., 9.4 mM KNO3 and the depletion of nitrogen) increased the levels and molecular diversity of anthocyanins. An expression analysis of the main regulatory and pathway genes showed that at conditions of higher concentrations of ammonium and total nitrogen, the expression levels of PAP1 and TT8 decreased, but the expression levels of LBD37, 38 and 39, three negative regulators of anthocyanin biosynthesis, increased. In addition, the expression levels of the main pathway genes decreased. In contrast, at conditions of lower concentrations of ammonium and total nitrogen, the expression levels of PAP1, TT8 and the main pathway genes increased, whereas those of LBD37, 38 and 39 decreased. These results show that nitrogen regulation of anthocyanin biosynthesis in red cells undergoes a mechanism by which nitrogen controls the expression of genes encoding both main components of the TTG1–GL3/TT8–PAP1 complex and negative regulators. Based on these observations, we propose that the regulatory mechanism of nitrogen may occur via two pathways to control the expression of genes encoding positive and negative regulators in red pap1-D cells.
机译:氮养分可以调节拟南芥中花色苷的生物合成。在这项研究中,我们报告了TPG1-GL3 / TT8-PAP1在红色pap1-D细胞中激活花色苷生物合成的氮调控。为了了解氮调节的机制,我们采用了红色的pap1-D细胞和野生型细胞(作为对照)来研究不同氮处理对花色苷生物合成的影响。通常,较高的铵浓度和较高的总氮含量(例如,由NH4 NO3 和KNO3 组成的总氮为58.8和29.8 mM)降低了花色苷的含量和分子多样性。相反,较低的铵浓度和总氮条件(例如9.4 mM KNO3 和氮的消耗)增加了花色苷的水平和分子多样性。对主要调节基因和途径基因的表达分析表明,在铵和总氮浓度较高的条件下,PAP1和TT8的表达水平下降,但LBD37、38和39的表达水平是花色苷生物合成的三个负调节子,增加。另外,主要途径基因的表达水平降低。相反,在铵和总氮浓度较低的条件下,PAP1,TT8和主要途径基因的表达水平升高,而LBD37、38和39的表达水平降低。这些结果表明,红细胞中花青素生物合成的氮调节经历了一种机制,氮通过该机制控制编码TTG1-GL3 / TT8-PAP1复合体和负调节剂的基因的表达。基于这些观察,我们建议氮的调节机制可能通过两种途径来控制,以控制红色pap1-D细胞中编码正负调节剂的基因的表达。

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