State Key Laboratory of Crop Biology, MOA Key Laboratory of Horticultural Crop Biology and Germplasm Innovation, College of Horticulture Science and Engineering, Shandong Agricultural University, Tai-An, Shandong, China.
College of Biological and Agricultural Engineering, Weifang University, Weifang, Shandong, China.
Plant Cell Environ. 2018 Nov;41(11):2678-2692. doi: 10.1111/pce.13393. Epub 2018 Aug 3.
Phytohormone abscisic acid (ABA) induces anthocyanin biosynthesis; however, the underlying molecular mechanism is less known. In this study, we found that the apple MYB transcription factor MdMYB1 activated anthocyanin biosynthesis in response to ABA. Using a yeast screening technique, we isolated MdbZIP44, an ABA-induced bZIP transcription factor in apple, as a co-partner with MdMYB1. MdbZIP44 promoted anthocyanin accumulation in response to ABA by enhancing the binding of MdMYB1 to the promoters of downstream target genes. Furthermore, we identified MdBT2, a BTB protein, as an MdbZIP44-interacting protein. A series of molecular, biochemical, and genetic analysis suggested that MdBT2 degraded MdbZIP44 protein through the Ubiquitin-26S proteasome system, thus inhibiting MdbZIP44-modulated anthocyanin biosynthesis. Taken together, we reveal a novel working mechanism of MdbZIP44-mediated anthocyanin biosynthesis in response to ABA.
植物激素脱落酸(ABA)诱导花青素生物合成;然而,其潜在的分子机制知之甚少。在这项研究中,我们发现苹果 MYB 转录因子 MdMYB1 响应 ABA 激活花青素生物合成。我们使用酵母筛选技术,分离出苹果中受 ABA 诱导的 bZIP 转录因子 MdbZIP44,作为与 MdMYB1 的共同伙伴。MdbZIP44 通过增强 MdMYB1 与下游靶基因启动子的结合,促进 ABA 诱导的花青素积累。此外,我们鉴定出 MdBT2 是 MdbZIP44 的相互作用蛋白。一系列分子、生化和遗传分析表明,MdBT2 通过泛素-26S 蛋白酶体系统降解 MdbZIP44 蛋白,从而抑制 MdbZIP44 调节的花青素生物合成。总之,我们揭示了 MdbZIP44 介导的 ABA 响应花青素生物合成的新工作机制。