Zhou D X, Li Y F, Rocipon M, Mache R
Laboratoire de Biologie Moléculaire Végétale, Centre National de la Recherche Scientifique, Unité de Recherche Associée 1178, Université J. Fourier, Grenoble, France.
J Biol Chem. 1992 Nov 25;267(33):23515-9.
The nuclear gene rps1 coding for the spinach plastid ribosomal protein CS1 exhibits both a constitutive and leaf-specific expression pattern. In contrast to other chloroplast-related genes like rbcS and cab, the leaf induction of rps1 expression is light-independent. These unique features of rps1 expression provide good models to study the mechanisms regulating plastid development and differentiation in higher plants. We report on the identification of a spinach leaf nuclear factor, designated S1F, interacting with the rps1 promoter. The S1F binding site is conserved in the promoter region of many plastid-related genes, including rbcS, cab, and rpl21. A binding activity similar to S1F was detected in nuclear extract from dark-grown de-differentiated soybean suspension cells. Through site-specific mutagenesis and transient expression in soybean cell protoplasts, we show that the S1F binding site is a negative element down-regulating the promoter activity of rps1. A ligated tetramer of S1F site was able to repress activity of the cauliflower mosaic virus 35 S promoter extending the negative function of the S1F binding site on promoter activity.
编码菠菜质体核糖体蛋白CS1的核基因rps1呈现出组成型和叶片特异性的表达模式。与其他叶绿体相关基因如rbcS和cab不同,rps1表达的叶片诱导不依赖于光。rps1表达的这些独特特征为研究高等植物中质体发育和分化的调控机制提供了良好的模型。我们报道了一种菠菜叶片核因子的鉴定,该因子命名为S1F,它与rps1启动子相互作用。S1F结合位点在许多叶绿体相关基因的启动子区域是保守的,包括rbcS、cab和rpl21。在黑暗培养的去分化大豆悬浮细胞的核提取物中检测到一种与S1F相似的结合活性。通过定点诱变和在大豆细胞原生质体中的瞬时表达,我们表明S1F结合位点是下调rps1启动子活性的负调控元件。S1F位点的连接四聚体能够抑制花椰菜花叶病毒35S启动子的活性,从而扩展了S1F结合位点对启动子活性的负调控功能。