Bioproduction Research Institute, National Institute of Advanced Industrial Science and Technology, Higashi 1-1-1, Tsukuba 305-8562, Japan.
Plant Cell. 2013 May;25(5):1609-24. doi: 10.1105/tpc.113.110783. Epub 2013 May 24.
The waxy plant cuticle protects cells from dehydration, repels pathogen attack, and prevents organ fusion during development. The transcription factor WAX INDUCER1/SHINE1 (WIN1/SHN1) regulates the biosynthesis of waxy substances in Arabidopsis thaliana. Here, we show that the MIXTA-like MYB transcription factors MYB106 and MYB16, which regulate epidermal cell morphology, also regulate cuticle development coordinately with WIN1/SHN1 in Arabidopsis and Torenia fournieri. Expression of a MYB106 chimeric repressor fusion (35S:MYB106-SRDX) and knockout/down of MYB106 and MYB16 induced cuticle deficiencies characterized by organ adhesion and reduction of epicuticular wax crystals and cutin nanoridges. A similar organ fusion phenotype was produced by expression of a WIN1/SHN1 chimeric repressor. Conversely, the dominant active form of MYB106 (35S:MYB106-VP16) induced ectopic production of cutin nanoridges and increased expression of WIN1/SHN1 and wax biosynthetic genes. Microarray experiments revealed that MYB106 and WIN1/SHN1 regulate similar sets of genes, predominantly those involved in wax and cutin biosynthesis. Furthermore, WIN1/SHN1 expression was induced by MYB106-VP16 and repressed by MYB106-SRDX. These results indicate that the regulatory cascade of MIXTA-like proteins and WIN1/SHN1 coordinately regulate cutin biosynthesis and wax accumulation. This study reveals an additional key aspect of MIXTA-like protein function and suggests a unique relationship between cuticle development and epidermal cell differentiation.
蜡质植物表皮层可以保护细胞免受脱水、抵御病原体的攻击,并在发育过程中防止器官融合。转录因子 WAX INDUCER1/SHINE1(WIN1/SHN1)调节拟南芥中蜡质物质的生物合成。在这里,我们发现调节表皮细胞形态的 MIXTA 样 MYB 转录因子 MYB106 和 MYB16 与 WIN1/SHN1 一起协调调节拟南芥和蓝猪耳的表皮层发育。表达 MYB106 嵌合阻遏融合蛋白(35S:MYB106-SRDX)和 MYB106 和 MYB16 的敲除/下调导致表皮层缺陷,表现为器官粘连和减少角质层蜡晶体和角质纳米脊。WIN1/SHN1 嵌合阻遏物的表达产生了类似的器官融合表型。相反,MYB106 的显性激活形式(35S:MYB106-VP16)诱导角质纳米脊的异位产生,并增加 WIN1/SHN1 和蜡生物合成基因的表达。微阵列实验表明,MYB106 和 WIN1/SHN1 调节相似的基因集,主要是参与蜡质和角质生物合成的基因。此外,WIN1/SHN1 的表达被 MYB106-VP16 诱导,被 MYB106-SRDX 抑制。这些结果表明,MIXTA 样蛋白和 WIN1/SHN1 的调控级联协同调节角质生物合成和蜡质积累。本研究揭示了 MIXTA 样蛋白功能的另一个关键方面,并暗示了表皮层发育和表皮细胞分化之间的独特关系。