Koppen Arjen, Ait-Aissa Rachida, Koster Jan, van Sluis Peter G, Ora Ingrid, Caron Huib N, Volckmann Richard, Versteeg Rogier, Valentijn Linda J
Department of Human Genetics, Academic Medical Center, University of Amsterdam, P.O. Box 22700, 1100 DE Amsterdam, The Netherlands.
Eur J Cancer. 2007 Nov;43(16):2413-22. doi: 10.1016/j.ejca.2007.07.024. Epub 2007 Sep 10.
The c-Myc and MYCN oncogenes strongly induce cell proliferation. Although a limited series of cell cycle genes were found to be induced by the myc transcription factors, it is still unclear how they mediate the proliferative phenotype. We therefore analysed a neuroblastoma cell line with inducible MYCN expression. We found that all members of the minichromosome maintenance complex (MCM2-7) and MCM8 and MCM10 were up-regulated by MYCN. Expression profiling of 110 neuroblastoma tumours revealed that these genes strongly correlated with MYCN expression in vivo. Extensive chromatin immunoprecipitation experiments were performed to investigate whether the MCM genes were primary MYCN targets. MYCN was bound to the proximal promoters of the MCM2 to -8 genes. These data suggest that MYCN stimulates the expression of not only MCM7, which is a well defined MYCN target gene, but also of the complete minichromosome maintenance complex.
c-Myc和MYCN癌基因强烈诱导细胞增殖。尽管发现有限系列的细胞周期基因可被myc转录因子诱导,但它们如何介导增殖表型仍不清楚。因此,我们分析了一种具有可诱导MYCN表达的神经母细胞瘤细胞系。我们发现微小染色体维持复合体(MCM2 - 7)的所有成员以及MCM8和MCM10均被MYCN上调。对110例神经母细胞瘤肿瘤的表达谱分析显示,这些基因在体内与MYCN表达密切相关。进行了广泛的染色质免疫沉淀实验,以研究MCM基因是否为MYCN的直接靶标。MYCN与MCM2至 - 8基因的近端启动子结合。这些数据表明,MYCN不仅刺激已明确的MYCN靶基因MCM7的表达,还刺激整个微小染色体维持复合体的表达。