Centre for Forest Biology and Department of Biology, University of Victoria, Victoria, British Columbia, Canada V8W 3N5 (A.M.J., D.M., R.M., A.G., K.Y., V.W., L.T., C.P.C.).
Max-Planck Institute for Chemical Ecology, Department of Biochemistry, 07745 Jena, Germany (M.R., J.G.).
Plant Physiol. 2017 May;174(1):154-171. doi: 10.1104/pp.16.01962. Epub 2017 Mar 27.
The accumulation of proanthocyanidins is regulated by a complex of transcription factors composed of R2R3 MYB, basic helix-loop-helix, and WD40 proteins that activate the promoters of biosynthetic genes. In poplar (genus ), MYB134 is known to regulate proanthocyanidin biosynthesis by activating key flavonoid genes. Here, we characterize a second MYB regulator of proanthocyanidins, MYB115. Transgenic poplar overexpressing MYB115 showed a high-proanthocyanidin phenotype and reduced salicinoid accumulation, similar to the effects of MYB134 overexpression. Transcriptomic analysis of MYB115- and MYB134-overexpressing poplar plants identified a set of common up-regulated genes encoding proanthocyanidin biosynthetic enzymes and several novel uncharacterized MYB transcriptional repressors. Transient expression experiments demonstrated the capacity of both MYB134 and MYB115 to activate flavonoid promoters, but only in the presence of a basic helix-loop-helix cofactor. Yeast two-hybrid experiments confirmed the direct interaction of these transcription factors. The unexpected identification of dihydromyricetin in leaf extracts of both MYB115- and MYB134-overexpressing poplar led to the discovery of enhanced flavonoid B-ring hydroxylation and an increased proportion of prodelphinidins in proanthocyanidin of the transgenics. The dramatic hydroxylation phenotype of MYB115 overexpressors is likely due to the up-regulation of both flavonoid 3',5'-hydroxylases and cytochrome Overall, this work provides new insight into the complexity of the gene regulatory network for proanthocyanidin synthesis in poplar.
原花青素的积累受到由 R2R3 MYB、碱性螺旋-环-螺旋和 WD40 蛋白组成的转录因子复合物的调节,该复合物激活生物合成基因的启动子。在杨属(Populus)中,MYB134 被认为通过激活关键类黄酮基因来调节原花青素的生物合成。在这里,我们鉴定了原花青素的第二个 MYB 调节因子 MYB115。过表达 MYB115 的转基因杨树表现出高原花青素表型和降低的水杨苷积累,类似于 MYB134 过表达的效果。对 MYB115 和 MYB134 过表达的杨树进行转录组分析,确定了一组共同上调的基因,这些基因编码原花青素生物合成酶和几个新的未鉴定的 MYB 转录抑制子。瞬时表达实验表明,MYB134 和 MYB115 都能够激活类黄酮启动子,但仅在存在碱性螺旋-环-螺旋共因子的情况下。酵母双杂交实验证实了这些转录因子的直接相互作用。在 MYB115 和 MYB134 过表达的杨树叶片提取物中意外发现二氢杨梅素,导致发现黄酮类化合物 B 环羟化增强,以及原花青素中前花青素的比例增加。MYB115 过表达体的剧烈羟化表型可能是由于黄酮类化合物 3',5'-羟化酶和细胞色素的上调。总的来说,这项工作为杨树中原花青素合成的基因调控网络的复杂性提供了新的见解。