Zhao Jinfeng, Zhang Wenhui, Zhao Yang, Gong Ximing, Guo Lei, Zhu Guoli, Wang Xuechen, Gong Zhizhong, Schumaker Karen S, Guo Yan
State Key Laboratory of Plant Physiology and Biochemistry, College of Biological Sciences, China Agricultural University, Beijing 100094, China.
Plant Cell. 2007 Nov;19(11):3805-18. doi: 10.1105/tpc.106.048900. Epub 2007 Nov 9.
We report that the Arabidopsis thaliana mutant sensitive to ABA and drought2 (sad2), which harbors a T-DNA insertion in an importin beta-like gene, is more tolerant to UV-B radiation than the wild type. Analysis of cyclobutane pyrimidine dimer accumulation revealed that less DNA damage occurred in sad2 than in the wild type during UV-B treatment. No significant growth difference was observed between sad2 and the wild type when treated with the genotoxic drug methyl methanesulfonate, suggesting that SAD2 functions in UV-B protection rather than in DNA damage repair. Whereas the R2R3-type transcription repressor MYB4 has previously been shown to negatively regulate the transcription of cinnamate 4-hydroxylase (C4H) and thus to regulate the synthesis of sinapate esters, expression of both MYB4 and C4H and accumulation of UV-absorbing compounds were significantly higher in sad2 than in the wild type. MYB4 did not localize to the nucleus in the sad2 mutant, suggesting that SAD2 is required for MYB4 nuclear trafficking. SAD2 and MYB4 coimmunoprecipitated, indicating that these proteins localize in the same complex in vivo. MYB4 protein specifically bound to its own promoter in gel shift assays and repressed its own expression, demonstrating that MYB4 protein and mRNA are part of a negative autoregulatory loop. This feedback loop is altered in the sad2 mutant due to the absence of MYB4 protein in the nucleus, leading to the constitutive expression of MYB4 and C4H and resulting in accumulation of UV-absorbing pigments that shield the plant from UV-B radiation.
我们报道,拟南芥对脱落酸和干旱敏感2(sad2)突变体在一个类输入蛋白β基因中存在T-DNA插入,该突变体比野生型对UV-B辐射更具耐受性。对环丁烷嘧啶二聚体积累的分析表明,在UV-B处理期间,sad2中发生的DNA损伤比野生型少。在用遗传毒性药物甲磺酸甲酯处理时,未观察到sad2与野生型之间有显著的生长差异,这表明SAD2在UV-B保护而非DNA损伤修复中起作用。此前已表明,R2R3型转录抑制因子MYB4负调控肉桂酸4-羟化酶(C4H)的转录,从而调控芥子酸酯的合成,而sad2中MYB4和C4H的表达以及紫外线吸收化合物的积累均显著高于野生型。在sad2突变体中,MYB4未定位到细胞核,这表明SAD2是MYB4核运输所必需的。SAD2和MYB4进行了共免疫沉淀,表明这些蛋白质在体内定位于同一复合物中。在凝胶迁移实验中,MYB4蛋白特异性结合其自身的启动子并抑制其自身表达,这表明MYB4蛋白和mRNA是负自调节环的一部分。由于细胞核中不存在MYB4蛋白,该反馈环在sad2突变体中发生改变,导致MYB4和C4H的组成型表达,并导致紫外线吸收色素的积累,从而保护植物免受UV-B辐射。