Hainan Key Laboratory for Sustainable Utilization of Tropical Bioresources and College of Biology, Institute of Tropical Agriculture and Forestry, Hainan University, Haikou, 570228, China.
Leeds University.
J Exp Bot. 2017 Oct 13;68(17):4997-5006. doi: 10.1093/jxb/erx305.
Similar to the situation in animals, melatonin biosynthesis is regulated by four sequential enzymatic steps in plants. Although the melatonin synthesis genes have been identified in various plants, the upstream transcription factors of them remain unknown. In this study on cassava (Manihot esculenta), we found that MeWRKY79 and heat-shock transcription factor 20 (MeHsf20) targeted the W-box and the heat-stress elements (HSEs) in the promoter of N-acetylserotonin O-methyltransferase 2 (MeASMT2), respectively. The interaction between MeWRKY79, MeHsf20, and the MeASMT2 promoter was evidenced by the activation of promoter activity and chromatin immunoprecipitation (ChIP) in cassava protoplasts, and by an in vitro electrophoretic mobility shift assay (EMSA). The transcripts of MeWRKY79, MeHsf20, and MeASMT2 were all regulated by a 22-amino acid flagellin peptide (flg22) and by Xanthomonas axonopodis pv manihotis (Xam). In common with the phenotype of MeASMT2, transient expression of MeWRKY79 and MeHsf20 in Nicotiana benthamiana leaves conferred improved disease resistance. Through virus-induced gene silencing (VIGS) in cassava, we found that MeWRKY79- and MeHsf20-silenced plants showed lower transcripts of MeASMT2 and less accumulation of melatonin, which resulted in disease sensitivity that could be reversed by exogenous melatonin. Taken together, these results indicate that MeASMT2 is a target of MeWRKY79 and MeHsf20 in plant disease resistance. This study identifies novel upstream transcription factors of melatonin synthesis genes in cassava, thus extending our knowledge of the complex modulation of melatonin synthesis in plant defense.
类似于动物中的情况,植物中的褪黑素生物合成受四个连续的酶促步骤调节。尽管已经在各种植物中鉴定出了褪黑素合成基因,但它们的上游转录因子仍然未知。在这项关于木薯(Manihot esculenta)的研究中,我们发现 MeWRKY79 和热休克转录因子 20(MeHsf20)分别靶向 N-乙酰血清素 O-甲基转移酶 2(MeASMT2)启动子中的 W 框和热应激元件(HSEs)。MeWRKY79、MeHsf20 和 MeASMT2 启动子之间的相互作用通过木薯原生质体中启动子活性和染色质免疫沉淀(ChIP)的激活以及体外电泳迁移率变动分析(EMSA)得到证实。MeWRKY79、MeHsf20 和 MeASMT2 的转录均受 22 个氨基酸鞭毛肽(flg22)和黄单胞菌木薯致病变种(Xam)的调节。与 MeASMT2 的表型相同,MeWRKY79 和 MeHsf20 在烟草原生质体中的瞬时表达赋予了对疾病的抗性。通过木薯中的病毒诱导基因沉默(VIGS),我们发现 MeWRKY79 和 MeHsf20 沉默的植物中 MeASMT2 的转录物水平较低,褪黑素积累较少,导致疾病敏感性增加,而外源性褪黑素可以逆转这种敏感性。综上所述,这些结果表明 MeASMT2 是植物抗病性中 MeWRKY79 和 MeHsf20 的靶标。本研究鉴定了木薯中褪黑素合成基因的新型上游转录因子,从而扩展了我们对植物防御中褪黑素合成复杂调节的认识。