Satoh J, Baba K, Nakahira Y, Shiina T, Toyoshima Y
Graduate School of Human and Environmental Studies, Kyoto University, Sakyo-ku, Japan.
Plant Mol Biol. 1997 Jan;33(2):267-78. doi: 10.1023/a:1005799001271.
Dynamical aspects of three chloroplast promoters responding to change in light condition were examined in mature chloroplasts of wheat (Triticum aestivum) by in vitro transcription. The wheat psbD/C operon has four distinct promoters, two of which named as D/C-3 and D/C-4 promoters dominantly function in mature chloroplasts to produce the mRNAs encoding D2/CP43 and CP43 alone, respectively. Activity of the D/C-3 promoter in mature chloroplasts was reduced to less than 30% by 24 h dark adaptation and recovered by re-illumination to the original level within 30 to 60 min. The activation of the D/C-3 promoter which requires de novo cytoplasmic protein synthesis was induced by low fluence of light (e.g. 16 microE m(-2) s(-1)), but the extent of activation increased with increasing light fluence. The accumulation of mRNAs from the D/C-3 promoter saturated at 2- to 3-fold higher level within 2 h when the dark-adapted seedlings were transferred to the light at 72 microE m(-2) s(-1), concomitant with the increase in rate of D2 synthesis, suggesting that synthesis of D2 in mature chloroplasts is controlled via the D/C-3 promoter activity in a light-dependent way. Activity of the D/C-4 promoter slightly increased in the dark and decreased in the light. Effect of light on the psbA promoter activity was not observed at all in mature chloroplasts. In vitro transcriptional analysis of the D/C-3 promoter with 5' deletion mutations revealed that at least two cis elements which are located within the sequences of -78 to -47 and -46 to -29 of the transcription initiation site, respectively, act as enhancing elements in the D/C-3 promoter. The light-switching element of the transcription, however, was suggested to be located in the core promoter sequence downstream of the -35 element.
通过体外转录,研究了小麦(Triticum aestivum)成熟叶绿体中三个响应光照条件变化的叶绿体启动子的动力学特性。小麦psbD/C操纵子有四个不同的启动子,其中两个分别命名为D/C-3和D/C-4启动子,在成熟叶绿体中主要发挥作用,分别单独产生编码D2/CP43和CP43的mRNA。经过24小时暗适应后,成熟叶绿体中D/C-3启动子的活性降低到30%以下,重新光照后在30至60分钟内恢复到原始水平。需要从头合成细胞质蛋白的D/C-3启动子的激活是由低光通量(如16 μE m(-2) s(-1))诱导的,但激活程度随着光通量的增加而增加。当暗适应的幼苗在72 μE m(-2) s(-1)的光照下转移到光照条件下时,来自D/C-3启动子的mRNA在2小时内积累到比原来高2至3倍的饱和水平,同时D2合成速率增加,这表明成熟叶绿体中D2的合成是通过D/C-3启动子活性以光依赖的方式控制的。D/C-4启动子的活性在黑暗中略有增加,在光照下降低。在成熟叶绿体中完全未观察到光对psbA启动子活性的影响。对具有5'缺失突变的D/C-3启动子进行体外转录分析表明,至少两个顺式元件分别位于转录起始位点的-78至-47和-46至-29序列内,作为D/C-3启动子中的增强元件。然而,转录的光开关元件被认为位于-35元件下游的核心启动子序列中。