Villain P, Clabault G, Mache R, Zhou D X
Laboratoire de Biologie Moléculaire Végétale, Centre National de la Recherche Scientifique, Unité de Recherche Associée 1178, Université Joseph Fourier, Grenoble, France.
J Biol Chem. 1994 Jun 17;269(24):16626-30.
Nuclear genes encoding plastid ribosomal proteins are more highly expressed in leaves than in roots. This leaf-specific induction seems to be light-independent. We have previously characterized a spinach nuclear factor S1F binding to a cis-element within the rps1 promoter, which negatively regulates both the rps1 and the cauliflower mosaic virus 35S promoters in transient expression assays. Here, we show that the S1F binding site is related to but different from the light-responsive Box II of the pea rbcS-3A promoter, which is recognized by the nuclear factor GT-1. Transgenic plant analyses showed that the S1F site tissue-specifically represses the rps1 promoter in roots as well as in etiolated seedlings. We suggest that the GT-1-related S1F binding site is responsible, at least in part, for the transcriptional repression of rps1 in nonphotosynthetic tissues such as roots.
编码质体核糖体蛋白的核基因在叶片中的表达水平高于根中。这种叶片特异性诱导似乎与光照无关。我们之前鉴定了一种菠菜核因子S1F,它能与rps1启动子内的一个顺式元件结合,在瞬时表达分析中,该因子对rps1和花椰菜花叶病毒35S启动子均具有负调控作用。在此,我们表明S1F结合位点与豌豆rbcS - 3A启动子的光响应元件Box II相关,但又有所不同,后者可被核因子GT - 1识别。转基因植物分析表明,S1F位点在根以及黄化幼苗中对rps1启动子具有组织特异性抑制作用。我们认为,与GT - 1相关的S1F结合位点至少部分负责rps1在根等非光合组织中的转录抑制。