Nakahira Y, Baba K, Yoneda A, Shiina T, Toyoshima Y
Graduate School of Human and Environmental Studies, Kyoto University, Yoshida-nihonmatu-cho, Sakyo-ku, Kyoto 606-8501, Japan.
Plant Physiol. 1998 Nov;118(3):1079-88. doi: 10.1104/pp.118.3.1079.
The level of mRNAs derived from the plastid-encoded psbD light-responsive promoter (LRP) is controlled by a circadian clock(s) in wheat (Triticum aestivum). The circadian oscillations in the psbD LRP mRNA level persisted for at least three cycles in continuous light and for one cycle in continuous dark, with maxima in subjective morning and minima in subjective early night. In vitro transcription in chloroplast extracts revealed that the circadian cycles in the psbD LRP mRNA level were dominantly attributed to the circadian-regulated transcription of the psbD LRP. The effects of various mutations introduced into the promoter region on the psbD LRP activity in vitro suggest the existence of two positive elements located between -54 and -36, which generally enhance the transcription activity, and an anomalous core promoter structure lacking the functional "-35" element, which plays a crucial role in the circadian fluctuation and light dependency of psbD LRP transcription activity.
源自质体编码的psbD光响应启动子(LRP)的mRNA水平受小麦(Triticum aestivum)生物钟调控。在持续光照下,psbD LRP mRNA水平的昼夜节律振荡持续至少三个周期,在持续黑暗中持续一个周期,在主观早晨达到最大值,在主观深夜达到最小值。叶绿体提取物中的体外转录表明,psbD LRP mRNA水平的昼夜节律周期主要归因于psbD LRP的昼夜节律调控转录。启动子区域引入的各种突变对psbD LRP体外活性的影响表明,在-54至-36之间存在两个通常增强转录活性的正向元件,以及一个缺乏功能性“-35”元件的异常核心启动子结构,该结构在psbD LRP转录活性的昼夜节律波动和光依赖性中起关键作用。