Centre for Forest Biology & Department of Biology, University of Victoria, 3800 Finnerty Road, Victoria, BC, V8P 5C2, Canada.
Department of Biochemistry, Max-Planck Institute for Chemical Ecology, Hans-Knöll Strasse 8, 07745, Jena, Germany.
Plant J. 2018 Dec;96(5):949-965. doi: 10.1111/tpj.14081. Epub 2018 Oct 8.
The phenylpropanoid pathway leads to the production of many important plant secondary metabolites including lignin, chlorogenic acids, flavonoids, and phenolic glycosides. Early studies have demonstrated that flavonoid biosynthesis is transcriptionally regulated, often by a MYB, bHLH, and WDR transcription factor complex. In poplar, several R2R3 MYB transcription factors are known to be involved in flavonoid biosynthesis. Previous work determined that poplar MYB134 and MYB115 are major activators of the proanthocyanidin pathway, and also induce the expression of repressor-like MYB transcription factors. Here we characterize two new repressor MYBs, poplar MYB165 and MYB194, paralogs which comprise a subgroup of R2R3-MYBs distinct from previously reported poplar repressors. Both MYB165 and MYB194 repressed the activation of flavonoid promoters by MYB134 in transient activation assays, and both interacted with a co-expressed bHLH transcription factor, bHLH131, in yeast two-hybrid assays. Overexpression of MYB165 and MYB194 in hybrid poplar resulted in greatly reduced accumulation of several phenylpropanoids including anthocyanins, proanthocyanidins, phenolic glycosides, and hydroxycinnamic acid esters. Transcriptome analysis of MYB165- and MYB194-overexpressing poplars confirmed repression of many phenylpropanoid enzyme genes. In addition, other MYB genes as well as several shikimate pathway enzyme genes were downregulated by MYB165-overexpression. By contrast, leaf aromatic amino acid concentrations were greater in MYB165-overexpressing poplars. Our findings indicate that MYB165 is a major repressor of the flavonoid and phenylpropanoid pathway in poplar, and may also affect the shikimate pathway. The coordinated action of repressor and activator MYBs could be important for the fine tuning of proanthocyanidin biosynthesis during development or following stress.
苯丙烷途径导致许多重要的植物次生代谢物的产生,包括木质素、绿原酸、类黄酮和酚糖苷。早期的研究表明,类黄酮生物合成是转录调控的,通常由一个 MYB、bHLH 和 WDR 转录因子复合物调控。在杨树中,有几个 R2R3 MYB 转录因子被认为参与了类黄酮的生物合成。先前的工作确定杨树 MYB134 和 MYB115 是原花青素途径的主要激活子,同时也诱导了抑制子样 MYB 转录因子的表达。在这里,我们描述了两个新的抑制子 MYB,杨树 MYB165 和 MYB194,它们是 R2R3-MYB 的旁系同源物,与之前报道的杨树抑制子不同。MYB165 和 MYB194 都在瞬时激活测定中抑制了 MYB134 对类黄酮启动子的激活,并且在酵母双杂交测定中都与共表达的 bHLH 转录因子 bHLH131 相互作用。在杂种杨中过表达 MYB165 和 MYB194 导致几种苯丙烷类物质,包括花青素、原花青素、酚糖苷和羟基肉桂酸酯的积累大大减少。MYB165 和 MYB194 过表达杨树的转录组分析证实了许多苯丙烷酶基因的抑制。此外,其他 MYB 基因和几种莽草酸途径酶基因也被 MYB165 过表达下调。相比之下,MYB165 过表达的杨树叶片芳香族氨基酸浓度更高。我们的研究结果表明,MYB165 是杨树中黄酮类和苯丙烷途径的主要抑制剂,也可能影响莽草酸途径。抑制剂和激活剂 MYB 的协调作用对于发育过程中或应激后原花青素生物合成的精细调控可能很重要。