Onda Yayoi, Yagi Yusuke, Saito Yukiko, Takenaka Nobuhiro, Toyoshima Yoshinori
Department of Bioscience and Nano-biotechnology Research Centre, School of Science and Technology, Kwansei Gakuin University, Sanda, Hyogo, Japan.
Plant J. 2008 Sep;55(6):968-78. doi: 10.1111/j.1365-313X.2008.03567.x. Epub 2008 Jun 4.
In higher plants, multiple nuclear-encoded sigma factors activate select subsets of plastid gene promoters in a partially redundant manner. We analysed the light induction profiles of transcripts from six Arabidopsis sigma factor (AtSIG) genes in mature leaves, focusing on the effects of wavelength and intensity. Red-light illumination (660 nm) of dark-adapted plants strongly induced AtSIG1 transcripts, while blue-light illumination (470 nm) caused strong and rapid induction of AtSIG1 and AtSIG5 transcripts. The fluence response differed in blue-light-responsive rapid induction in AtSIG1 and AtSIG5. AtSIG1 transcripts increased to plateau with a threshold of 2 micromol m(-2) sec(-1) under all fluences examined (1-50 micromol m(-2) sec(-1)), and AtSIG5 transcripts were induced with a distinct two-phase profile, with the lower-fluence induction similar to that of AtSIG1 and further enhancement with increasing fluences greater than 10 micromol m(-2) sec(-1). Blue-light-receptor mutational analysis revealed that AtSIG5-specific two-phase induction is mediated through cryptochrome 1 and cryptochrome 2 at lower fluences and more significantly through cryptochrome 1 at higher fluences. In mature chloroplasts, the promoters of psbA and psbD are predominantly recognized by AtSIG5 among six sigma factors. Using a protoplast transient expression assay with AtSIG5-AtSIG1 chimeric genes, we present evidence that AtSIG5 contains determinants for activating the psbD blue-light-responsive promoter (BLRP) in region 4.2 rather than region 2.4. Amino acid scanning within AtSIG5 region 4.2 revealed that Asn484, but not Arg493, functions as a key residue for psbD BLRP activation. Arginine 493 may be involved in psbA promoter recognition.
在高等植物中,多个核编码的σ因子以部分冗余的方式激活质体基因启动子的特定子集。我们分析了成熟叶片中六个拟南芥σ因子(AtSIG)基因转录本的光诱导谱,重点关注波长和强度的影响。对暗适应的植物进行红光照射(660nm)强烈诱导AtSIG1转录本,而蓝光照射(470nm)则强烈且快速地诱导AtSIG1和AtSIG5转录本。AtSIG1和AtSIG5中蓝光响应快速诱导的光通量响应有所不同。在所有检测的光通量(1-50μmol m-2 s-1)下,AtSIG1转录本增加至平稳状态,阈值为2μmol m-2 s-1,而AtSIG5转录本以独特的两相谱被诱导,低光通量诱导类似于AtSIG1,并且随着光通量增加大于10μmol m-2 s-1进一步增强。蓝光受体突变分析表明,AtSIG5特异性的两相诱导在低光通量下通过隐花色素1和隐花色素2介导,在高光通量下更显著地通过隐花色素1介导。在成熟叶绿体中,psbA和psbD的启动子在六个σ因子中主要由AtSIG5识别。使用AtSIG5-AtSIG1嵌合基因的原生质体瞬时表达分析,我们提供证据表明AtSIG5在区域4.2而非区域2.4中包含激活psbD蓝光响应启动子(BLRP)的决定因素。AtSIG5区域4.2内的氨基酸扫描显示,Asn484而非Arg493作为psbD BLRP激活的关键残基起作用。精氨酸493可能参与psbA启动子的识别。