Weng Jing J, Yung Benjamin Y M
Cancer Biochemistry Laboratory, Department of Pharmacology, College of Medicine, Chang Gung University, 259 Wen-Hwa 1st Road, Kwei-San, Tao-Yuan 333, Taiwan, ROC.
Biochem Biophys Res Commun. 2005 Sep 30;335(3):826-31. doi: 10.1016/j.bbrc.2005.07.150.
Ectopic over-expression of nucleophosmin/B23 caused a marked up-regulation in the amounts of Yin Yang 1 (YY1) and proliferating cellular nuclear antigen (PCNA) proteins. Transfection with nucleophosmin/B23-targeting siRNA induced a decrease in the intracellular amounts of nucleophosmin/B23, YY1, and PCNA. PCNA expression and its promoter activity were attenuated either by nucleophosmin/B23-siRNA or YY1-siRNA. The ChIP assay showed that positive regulation of PCNA is achieved by binding of YY1 to the initiation site of PCNA promoter. The binding of YY1 to the PCNA promoter and histone H4 acetylation was significantly decreased in nucleophosmin/B23-siRNA-treated cells as compared to control vector-transfected cells. Mutation in YY1 binding site resulted in the loss of PCNA promoter activity and the binding of YY1 to the promoter. The results have indicated that YY1 binds to the initiation site of the PCNA promoter along with histone H4 acetylation, leading to transcriptional activity. We have demonstrated that nucleophosmin/B23 plays an important role in the regulation of PCNA through YY1.
核仁磷酸蛋白/B23的异位过表达导致阴阳1(YY1)和增殖细胞核抗原(PCNA)蛋白量显著上调。用靶向核仁磷酸蛋白/B23的小干扰RNA(siRNA)转染导致细胞内核仁磷酸蛋白/B23、YY1和PCNA量减少。PCNA表达及其启动子活性被核仁磷酸蛋白/B23-siRNA或YY1-siRNA减弱。染色质免疫沉淀(ChIP)分析表明,YY1与PCNA启动子起始位点结合实现对PCNA的正向调控。与对照载体转染细胞相比,在核仁磷酸蛋白/B23-siRNA处理的细胞中,YY1与PCNA启动子的结合以及组蛋白H4乙酰化显著降低。YY1结合位点的突变导致PCNA启动子活性丧失以及YY1与启动子的结合丧失。结果表明,YY1与组蛋白H4乙酰化一起结合到PCNA启动子的起始位点,导致转录活性。我们已经证明核仁磷酸蛋白/B23通过YY1在PCNA的调控中起重要作用。