Chabouté M E, Clément B, Sekine M, Philipps G, Chaubet-Gigot N
Institut de Biologie Moléculaire des Plantes du CNRS, Université Louis Pasteur, 12 rue du Général Zimmer, 67084 Strasbourg Cedex, France.
Plant Cell. 2000 Oct;12(10):1987-2000.
Ribonucleotide reductase (RNR) is a key enzyme involved in the DNA synthesis pathway. The RNR-encoded genes are cell cycle regulated and specifically expressed in S phase. The promoter of the RNR2 gene encoding for the small subunit was isolated from tobacco. Both in vivo and in vitro studies of the DNA-protein interactions in synchronized BY2 tobacco cells showed that two E2F-like motifs were involved in multiple specific complexes, some of which displayed cell cycle-regulated binding activities. Moreover, these two elements could specifically interact with a purified tobacco E2F protein. Involvement of the E2F elements in regulating the RNR2 promoter was checked by functional analyses in synchronized transgenic BY2 cells transformed with various RNR2 promoter constructs fused to the luciferase reporter gene. The two E2F elements were involved in upregulation of the promoter at the G1/S transition and mutation of both elements prevented any significant induction of the RNR promoter. In addition, one of the E2F elements sharing homology with the animal E2F/cell cycle-dependent element motif behaved like a repressor when outside of the S phase. These data provide evidence that E2F elements play a crucial role in cell cycle regulation of gene transcription in plants.
核糖核苷酸还原酶(RNR)是DNA合成途径中的一种关键酶。RNR编码基因受细胞周期调控,且在S期特异性表达。从小麦中分离出了编码小亚基的RNR2基因的启动子。对同步化的BY2小麦细胞中DNA-蛋白质相互作用的体内和体外研究均表明,两个E2F样基序参与了多种特异性复合物的形成,其中一些复合物表现出细胞周期调控的结合活性。此外,这两个元件可与纯化的小麦E2F蛋白特异性相互作用。通过对用与荧光素酶报告基因融合的各种RNR2启动子构建体转化的同步化转基因BY2细胞进行功能分析,检测了E2F元件在调控RNR2启动子中的作用。这两个E2F元件在G1/S期转变时参与启动子的上调,两个元件的突变阻止了RNR启动子的任何显著诱导。此外,与动物E2F/细胞周期依赖性元件基序具有同源性的一个E2F元件在S期之外时表现为阻遏物。这些数据证明E2F元件在植物基因转录的细胞周期调控中起关键作用。