Akiyama K, Kanda N, Yamada M, Tadokoro K, Matsunaga T, Nishi Y
Life Science Research Laboratory, Japan Tobacco Inc., Kanagawa.
Nucleic Acids Res. 1994 Jan 25;22(2):187-93. doi: 10.1093/nar/22.2.187.
In order to elucidate the initiation of the N-myc gene amplification, we have analyzed the original structures of the N-myc amplicons among 38 human neuroblastomas. Nineteen DNAs isolated from the N-myc amplicons recognized a continuous stretch totally encompassing a 5.5 megabase region spanning the normal N-myc gene. The co-amplification profiles with these DNAs showed that two of them, which mapped into a 300 kb region flanking the N-myc gene, were commonly amplified in most specimens, while others were differentially amplified among various subsets. These profiles enabled us to divide the N-myc amplicons into several groups and outline their original domains as a continuous stretches, pointing to the existence of 'consensus sites' for the ends of the initial domains in the original region. In one cell line, the domain was found to be several times larger than that of the derivative amplicon; and the rearranged sites identified within the amplicons, which showed no site specificity, were consistent with those deduced from the domain structure. These results lead to a model in which N-myc gene amplification is initiated at some consensus sites by a preferential mechanism and followed by a random loss of the domain structures during subsequent stages.
为了阐明N-myc基因扩增的起始机制,我们分析了38例人类神经母细胞瘤中N-myc扩增子的原始结构。从N-myc扩增子中分离出的19个DNA识别出一个连续的片段,该片段完全覆盖了跨越正常N-myc基因的5.5兆碱基区域。与这些DNA的共扩增图谱显示,其中两个定位在N-myc基因侧翼300 kb区域的DNA在大多数标本中共同扩增,而其他DNA在不同亚组中差异扩增。这些图谱使我们能够将N-myc扩增子分为几个组,并将它们的原始结构域勾勒为连续的片段,表明原始区域中初始结构域末端存在“共有位点”。在一个细胞系中,发现该结构域比衍生扩增子的结构域大几倍;并且在扩增子内鉴定出的重排位点没有位点特异性,与从结构域结构推导的位点一致。这些结果导致了一个模型,即N-myc基因扩增通过优先机制在一些共有位点起始,随后在后续阶段结构域结构随机丢失。