首页> 外文期刊>Plant Biotechnology Journal >Methylation of MdMYB1 locus mediated by RdDM pathway regulates anthocyanin biosynthesis in apple
【24h】

Methylation of MdMYB1 locus mediated by RdDM pathway regulates anthocyanin biosynthesis in apple

机译:RDDM途径介导的MDMYB1基因座的甲基化调节苹果中的花青素生物合成

获取原文
获取外文期刊封面目录资料

摘要

Methylation at the MdMYB1 promoter in apple sports has been reported as a regulator of the anthocyanin pathway, but little is known about how the locus is recognized by the methylation machinery to regulate anthocyanin accumulation. In this study, we analysed three differently coloured ‘Fuji’ apples and found that differences in the transcript levels of MdMYB1, which encodes a key regulator of anthocyanin biosynthesis, control the anthocyanin content (and therefore colour) in fruit skin. The CHH methylation levels in the MR3 region (?1246 to ?780) of the MdMYB1 promoter were found to be negatively correlated with MdMYB1 expression. Thus, they were ideal materials to study DNA methylation in apple sports. The protein of RNA‐directed DNA methylation (RdDM) pathway responsible for CHH methylation, MdAGO4, was found to interact with the MdMYB1 promoter. MdAGO4s can interact with MdRDM1 and MdDRM2s to form an effector complex, fulfilling CHH methylation. When MdAGO4s and MdDRM2s were overexpressed in apple calli and Arabidopsis mutants, those proteins increase the CHH methylation of AGO4‐binding sites. In electrophoretic mobility shift assays, MdAGO4s were found to specifically bind to sequence containing ATATCAGA. Knockdown of MdNRPE1 did not affect the binding of MdAGO4s to the c3 region of the MdMYB1 promoter in 35S::AGO4 calli. Taken together, our data show that the MdMYB1 locus is methylated through binding of MdAGO4s to the MdMYB1 promoter to regulate anthocyanin biosynthesis by the RdDM pathway.
机译:苹果运动中MDMyB1启动子的甲基化已被报告为花青素途径的调节剂,但是关于甲基化机械如何认识到甲基化机械如何调节花青素积累的稳定剂。在这项研究中,我们分析了三种不同颜色的“富士”苹果,发现MDMyB1的转录物水平的差异,它们编码了花青素生物合成的关键调节剂,控制果皮中的花青素含量(和因此颜色)。发现MDMYB1启动子的MR3区(α126至α780)中的CHH甲基化水平与MDMYB1表达呈负相关。因此,它们是在苹果运动中研究DNA甲基化的理想材料。发现负责CHH甲基化的RNA定向DNA甲基化(RDDM)途径的蛋白质与MDMYB1启动子相互作用。 MDAGO4S可以与MDRDM1和MDDRM2相互作用以形成效应复合物,满足CHH甲基化。当MDAGO4S和MDDRM2S在Apple Calli和Arabidopsis突变体中过表达时,那些蛋白质增加了前四次结合位点的CHH甲基化。在电泳迁移率移位测定中,发现MDAGO 4s特异性结合含有Atatcaga的序列。 MDNRPE1的敲低没有影响MDAGO4S与35s ::以前4个Calli的MDMyB1启动子C3区的结合。我们的数据占据,我们的数据表明,MDMyB1基因座通过MDAGO 4S与MDMYB1启动子的结合甲基化,以调节RDDM途径的花青素生物合成。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号