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UV-C response of the ribonucleotide reductase large subunit involves both E2F-mediated gene transcriptional regulation and protein subcellular relocalization in tobacco cells

机译:核糖核苷酸还原酶大亚基的UV-C反应涉及烟草细胞中E2F介导的基因转录调控和蛋白质亚细胞再定位

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摘要

E2F factors are implicated in various cellular processes including specific gene induction at the G_1/S transition of the cell cycle. We present in this study a novel regulatory aspect for the tobacco large subunit of ribonucleotide reductase (R1a) and its encoding gene (RNR1a) in the UV-C response. By structural analyses, two E2F sites were identified on the promoter of this gene. Functional analysis showed that, in addition to their role in the specific G_1/S induction of the RNR1a gene, both E2F sites were important for regulating specific RNR1a gene expression in response to UV-C irradiation in non-synchronized and synchronized cells. Concomitantly, western blot and cellular analyses showed an increase of a 60 kDa E2F factor and a transient translocation of a GFP-R1a protein fusion from cytoplasm to nucleus in response to UV irradiation.
机译:E2F因子与各种细胞过程有关,包括在细胞周期的G_1 / S过渡时的特定基因诱导。我们在这项研究中提出了一个新的调节方面,用于烟草核糖核苷酸还原酶大亚基(R1a)及其编码基因(RNR1a)的UV-C反应。通过结构分析,在该基因的启动子上鉴定了两个E2F位点。功能分析表明,除了它们在RNR1a基因的特异性G_1 / S诱导中的作用外,两个E2F位点对于调节非同步和同步细胞中的UV-C辐射对调节特定RNR1a基因表达也很重要。相应地,蛋白质印迹和细胞分析显示60 kDa E2F因子增加,并且响应于紫外线照射,GFP-R1a蛋白融合物从细胞质向细胞核瞬时转移。

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