Miyamoto Koji, Nishizawa Yoko, Minami Eiichi, Nojiri Hideaki, Yamane Hisakazu, Okada Kazunori
Department of Biosciences, Teikyo University, 1-1 Toyosatodai, Utsunomiya, Tochigi 320-8551, Japan; Biotechnology Research Center, The University of Tokyo, 1-1-1 Yayoi, Bunkyo-ku, Tokyo 113-8657, Japan.
Disease Resistant Crops Research Unit, GMO Research Center, National Institute of Agrobiological Sciences, 2-1-2 Kannondai, Tsukuba, Ibaraki 305-8602, Japan.
J Plant Physiol. 2015 Jan 15;173:19-27. doi: 10.1016/j.jplph.2014.09.001. Epub 2014 Sep 16.
Phytoalexins are antimicrobial specialised metabolites that are produced by plants in response to pathogen attack. Momilactones and phytocassanes are major diterpenoid phytoalexins in rice that are synthesised from geranylgeranyl diphosphate that is derived from the methylerythritol phosphate (MEP) pathway. We have previously reported that rice cells overexpressing the basic leucine zipper (bZIP) transcription factor OsTGAP1 exhibit a hyperaccumulation of momilactones and phytocassanes, with hyperinductive expression of momilactone and phytocassane biosynthetic genes and MEP pathway genes, upon response to a chitin oligosaccharide elicitor. For a better understanding of OsTGAP1-mediated regulation of diterpenoid phytoalexin production, we identified OsTGAP1-interacting proteins using yeast two-hybrid screening. Among the OsTGAP1-interacting protein candidates, a TGA factor OsbZIP79 was investigated to verify its physical interaction with OsTGAP1 and involvement in the regulation of phytoalexin production. An in vitro pull-down assay demonstrated that OsTGAP1 and OsbZIP79 exhibited a heterodimeric as well as a homodimeric interaction. A bimolecular fluorescence complementation analysis also showed the interaction between OsTGAP1 and OsbZIP79 in vivo. Intriguingly, whereas OsbZIP79 transactivation activity was observed in a transient reporter assay, the overexpression of OsbZIP79 resulted in suppression of the elicitor-inducible expression of diterpenoid phytoalexin biosynthetic genes, and thus caused a decrease in the accumulation of phytoalexin in rice cells. These results suggest that OsbZIP79 functions as a negative regulator of phytoalexin production triggered by a chitin oligosaccharide elicitor in rice cells, although it remains open under which conditions OsbZIP79 can work with OsTGAP1.
植保素是植物在受到病原体攻击时产生的抗菌特异性代谢产物。稻瘟菌素和植二萜植保素是水稻中的主要二萜类植保素,它们由源自甲基赤藓糖醇磷酸(MEP)途径的香叶基香叶基二磷酸合成。我们之前报道过,过表达碱性亮氨酸拉链(bZIP)转录因子OsTGAP1的水稻细胞在对几丁质寡糖激发子作出反应时,会出现稻瘟菌素和植二萜植保素的超积累,同时稻瘟菌素和植二萜植保素生物合成基因以及MEP途径基因的表达也会超诱导。为了更好地理解OsTGAP1介导的二萜类植保素产生的调控机制,我们通过酵母双杂交筛选鉴定了与OsTGAP1相互作用的蛋白。在与OsTGAP1相互作用的蛋白候选物中,对一个TGA因子OsbZIP79进行了研究,以验证其与OsTGAP1的物理相互作用以及在植保素产生调控中的作用。体外下拉试验表明,OsTGAP1和OsbZIP79表现出异源二聚体以及同源二聚体相互作用。双分子荧光互补分析也显示了OsTGAP1和OsbZIP79在体内的相互作用。有趣的是,虽然在瞬时报告试验中观察到了OsbZIP79的反式激活活性,但OsbZIP79的过表达导致二萜类植保素生物合成基因的激发子诱导表达受到抑制,从而导致水稻细胞中植保素积累减少。这些结果表明,OsbZIP79在水稻细胞中作为几丁质寡糖激发子触发的植保素产生的负调控因子发挥作用,尽管OsbZIP79在何种条件下能与OsTGAP1协同作用仍不明确。