Magome Hiroshi, Yamaguchi Shinjiro, Hanada Atsushi, Kamiya Yuji, Oda Kenji
Research Institute for Biological Sciences, 7549-1 Yoshikawa, Kayo, Okayama 716-1241, Japan.
Plant J. 2004 Mar;37(5):720-9. doi: 10.1111/j.1365-313x.2003.01998.x.
A novel gibberellin (GA)-deficient mutant designated dwarf and delayed-flowering 1 (ddf1) was isolated from a library of activation-tagged Arabidopsis. This mutant showed dwarfism and late-flowering, but the phenotype was rescued by exogenous GA3 like known mutants defective in GA biosynthesis. The contents of bioactive GA4 and GA1 were in fact decreased in ddf1 at least partially through the repression of biosynthetic steps catalyzed by GA 20-oxidase (GA20ox). Genetic and molecular analyses revealed that the ddf1 phenotypes are caused by increased or ectopic expression of a putative AP2 transcription factor. Overexpression of DDF2, encoding another putative AP2 transcription factor closely related to DDF1, also conferred the ddf1-like phenotype. Among genes encoding (putative) AP2 transcription factors in Arabidopsis, DDFs are phylogenetically close to dehydration-responsive element binding protein (DREB1)/C-repeat binding factor (CBF) genes, which are known to be involved in stress responses. The ddf1 mutation upregulates a stress-related gene RD29A. DDF1 mRNA is strongly induced by high-salinity stress within 1 h. Moreover, transgenic plants overexpressing DDF1 showed increased tolerance to high-salinity stress. These results suggest that DDF1 is involved in the regulation of GA biosynthesis and stress tolerance. The possible relation between the contents of endogenous GAs and acquisition of stress protection is discussed.
从激活标签拟南芥文库中分离出一个新的赤霉素(GA)缺陷型突变体,命名为矮化和开花延迟1(ddf1)。该突变体表现出矮化和晚花现象,但与已知的GA生物合成缺陷型突变体一样,其表型可通过外源GA3恢复。事实上,ddf1中生物活性GA4和GA1的含量至少部分通过抑制由GA 20-氧化酶(GA20ox)催化的生物合成步骤而降低。遗传和分子分析表明,ddf1的表型是由一个假定的AP2转录因子的表达增加或异位表达引起的。编码另一个与DDF1密切相关的假定AP2转录因子的DDF2的过表达也赋予了类似ddf1的表型。在拟南芥中编码(假定的)AP2转录因子的基因中,DDFs在系统发育上与脱水响应元件结合蛋白(DREB1)/C-重复结合因子(CBF)基因接近,已知这些基因参与应激反应。ddf1突变上调了一个与应激相关的基因RD29A。DDF1 mRNA在高盐胁迫1小时内被强烈诱导。此外,过表达DDF1的转基因植物对高盐胁迫的耐受性增强。这些结果表明,DDF1参与GA生物合成的调控和胁迫耐受性。本文还讨论了内源GA含量与获得胁迫保护之间的可能关系。