The Key Laboratory of Plant Resources/Beijing Botanical Garden, Institute of Botany, The Chinese Academy of Sciences, Beijing, 100093, China.
University of Chinese Academy of Sciences, Beijing, 100049, China.
Plant Cell Rep. 2017 Dec;36(12):1889-1902. doi: 10.1007/s00299-017-2203-3. Epub 2017 Sep 13.
GmMYB58 and GmMYB205 are key positive regulators that are involved in isoflavonoid biosynthesis in seeds of Glycine max, and they activate the expression of several structural genes in the isoflavonoid pathway. MYB transcription factors (TFs) are major regulators involved in flavonoid/isoflavonoid biosynthesis in many plant species. However, functions of most MYB TFs remain unknown in flavonoid/isoflavonoid pathway in Glycine max. In this study, we identified 321 MYB TFs by genome-wide searching, and further isolated and functionally characterized two MYB TFs, GmMYB58 and GmMYB205. The deduced GmMYB58 and GmMYB205 proteins contain highly conserved R2R3 repeat domain at the N-terminal region that is the signature motif of R2R3-type MYB TFs. GmMYB58 and GmMYB205 were highly expressed in early seed development stages than in the other tested organs. GmMYB58 and GmMYB205 GFP fusion proteins were found to be localized in the nucleus when they were transiently expressed in Arabidopsis thaliana mesophyll protoplast. Both GmMYB58 and GmMYB205 can activate the promoter activities of GmCHS, GmIFS2, and GmHID in the transient trans-activation assays, and the activation of GmHID by both GmMYB58 and GmMYB205 was further confirmed by yeast one-hybrid assay. In addition, over-expression of GmMYB58 and GmMYB205 resulted in significant increases in expression levels of several pathway genes in soybean hairy roots, in particular, IFS2 by more than fivefolds in GmMYB205-over-expressing lines. Moreover, isoflavonoid contents were remarkably enhanced in the GmMYB58 and GmMYB205 over-expressing hairy roots than in the control. Our results suggest that GmMYB58 and GmMYB205 are seed-specific TFs, and they can enhance isoflavonoid biosynthesis mainly through the regulation of GmIFS2 and GmHID in G. max.
GmMYB58 和 GmMYB205 是参与大豆种子中异黄酮生物合成的关键正调控因子,它们激活异黄酮途径中几个结构基因的表达。MYB 转录因子(TFs)是许多植物物种中黄酮类/异黄酮生物合成的主要调控因子。然而,在大豆的黄酮类/异黄酮途径中,大多数 MYB TFs 的功能仍然未知。在这项研究中,我们通过全基因组搜索鉴定了 321 个 MYB TFs,进一步分离和功能表征了两个 MYB TFs,GmMYB58 和 GmMYB205。推测的 GmMYB58 和 GmMYB205 蛋白在 N 端区域含有高度保守的 R2R3 重复结构域,这是 R2R3 型 MYB TFs 的特征基序。GmMYB58 和 GmMYB205 在早期种子发育阶段的表达量高于其他测试器官。当它们在拟南芥叶肉原生质体中瞬时表达时,GmMYB58 和 GmMYB205 的 GFP 融合蛋白被发现定位于细胞核内。在瞬时转录激活测定中,GmMYB58 和 GmMYB205 都可以激活 GmCHS、GmIFS2 和 GmHID 的启动子活性,并且酵母单杂交测定进一步证实了 GmMYB58 和 GmMYB205 对 GmHID 的激活。此外,GmMYB58 和 GmMYB205 的过表达导致大豆毛状根中几个途径基因的表达水平显著增加,特别是 GmMYB205 过表达系中 IFS2 的表达增加了五倍以上。此外,GmMYB58 和 GmMYB205 过表达毛状根中的异黄酮含量明显高于对照。我们的结果表明,GmMYB58 和 GmMYB205 是种子特异性 TF,它们可以通过调节大豆中的 GmIFS2 和 GmHID 来增强异黄酮的生物合成。