Shimizu N, Miura Y, Sakamoto Y, Tsutsui K
Faculty of Integrated Arts and Sciences, Hiroshima University, Hiroshima, 739-8521, Japan.
Cancer Res. 2001 Oct 1;61(19):6987-90.
Gene amplification plays a crucial role in the development of many human malignancies. Amplified genes are frequently localized on double minutes (DMs). We show here that plasmids bearing both a mammalian replication origin and a nuclear matrix attachment region were able to integrate into DMs if transfected to cells having DMs (COLO 320DM). Furthermore, these plasmids triggered the events leading to the de novo formation of the structure similar to DMs if transfected to the cells without DMs (COLO 320HSR or HeLa). Autonomous replication of these plasmids was suggested to be a prerequisite for these events to occur, because the presence of the origin sequences in the plasmids was required. The presence of matrix attachment region in the plasmids is also required for these events to occur, suggesting that matrix attachment plays an indispensable role in extrachromosomal replication. This model system will allow us to investigate the mechanism of gene amplification as well as to analyze the autonomous replication of the plasmid with mammalian replication origins.
基因扩增在许多人类恶性肿瘤的发展中起着关键作用。扩增的基因通常定位于双微体(DMs)上。我们在此表明,携带哺乳动物复制起点和核基质附着区域的质粒,如果转染到具有双微体的细胞(COLO 320DM)中,能够整合到双微体中。此外,如果将这些质粒转染到没有双微体的细胞(COLO 320HSR或HeLa)中,它们会引发导致从头形成类似于双微体结构的事件。这些质粒的自主复制被认为是这些事件发生的先决条件,因为质粒中需要有起点序列。质粒中核基质附着区域的存在对于这些事件的发生也是必需的,这表明核基质附着在染色体外复制中起着不可或缺的作用。这个模型系统将使我们能够研究基因扩增的机制,以及分析具有哺乳动物复制起点的质粒的自主复制。