Kalbina Irina, Strid Ake
Department of Science and Orebro Life Science Center, Orebro University, S-70182 Orebro, Sweden.
Plant Cell Environ. 2006 Sep;29(9):1783-93. doi: 10.1111/j.1365-3040.2006.01555.x.
Plant responses to supplementary UV-B irradiation have been reported to include formation of reactive oxygen species (ROS), hydrogen peroxide, in particular, and regulation by mitogen-activated protein kinase (MAPK) cascades which in turn are fine-tuned by MAPK phosphatases (MKPs). Here we present direct genetic evidence for the involvement of plasma membrane NADPH oxidase, a source of superoxide and hydrogen peroxide in the apoplasts, in UV-B signalling in Arabidopsis thaliana, by analysis of gene expression of the UV-B molecular markers in NADPH oxidase (atrbohD, F and DF) and MAP kinase phosphatase 1 (MKP1) knockout mutants (mkp1). Whereas the NADPH oxidase mutants were affected in UV-B-dependent CHS, PYROA and MEB5.2 gene expression, the mkp1 mutant was affected in the general expression pattern of the pathogenesis-related (PR) and PDF1.2 genes. The results indicate involvement of MKP1 in repressive action on gene expression of more general stress response pathways, similar to those activated by pathogen attack, while NADPH oxidase is involved in quantitative (rather than absolute) regulation of more UV-B-specific genes. The expressions of the molecular markers in the knockout mutant mkp1 and in its complemented lines (lines 6 and 10) were similar, as opposed to the responses of the corresponding wild-type Wassilewskija-4 (Ws-4). Lines 6 and 10 showed much higher MKP1 mRNA than Ws-4 but did not complement the mutant. This suggests a complex dependency of the MAPK phosporylation level of the PR and PDF1.2 genes. Both NADPH oxidase mutants and the mkp1 mutant phenotypically responded to UV-B by growth retardation.
据报道,植物对补充紫外线B辐射的反应包括活性氧(ROS)的形成,尤其是过氧化氢,以及丝裂原活化蛋白激酶(MAPK)级联反应的调节,而MAPK级联反应又由MAPK磷酸酶(MKP)进行微调。在这里,我们通过分析拟南芥中紫外线B分子标记物在NADPH氧化酶(atrbohD、F和DF)和MAP激酶磷酸酶1(MKP1)敲除突变体(mkp1)中的基因表达,提供了质膜NADPH氧化酶(质外体中超氧化物和过氧化氢的来源)参与拟南芥紫外线B信号传导的直接遗传学证据。虽然NADPH氧化酶突变体在紫外线B依赖的CHS、PYROA和MEB5.2基因表达方面受到影响,但mkp1突变体在病程相关(PR)和PDF1.2基因的总体表达模式方面受到影响。结果表明,MKP1参与对更一般应激反应途径基因表达的抑制作用,类似于病原体攻击激活的途径,而NADPH氧化酶参与对更多紫外线B特异性基因的定量(而非绝对)调节。敲除突变体mkp1及其互补系(6号和10号线)中分子标记物的表达与相应野生型Wassilewskija-4(Ws-4)的反应相反,相似。6号和10号线显示出比Ws-4高得多的MKP1 mRNA,但不能互补突变体。这表明PR和PDF1.2基因的MAPK磷酸化水平存在复杂的依赖性。NADPH氧化酶突变体和mkp1突变体在表型上都通过生长迟缓对紫外线B作出反应。