Shimizu N, Ochi T, Itonaga K
Faculty of Integrated Arts and Sciences, Hiroshima University, Hiroshima 739-8521, Japan.
Exp Cell Res. 2001 Aug 15;268(2):201-10. doi: 10.1006/excr.2001.5286.
Amplified genes in many human cancer cells usually localize at the extrachromosomal double minutes (DMs). In the present study, we show that multiple DMs in the human colorectal tumor COLO 320DM line replicated semisynchronously during the early S phase. On the other hand, during longer passage of the cells with DMs, cells with the amplified genes at the chromosomal homogeneously staining region (HSR) generally dominate the population. We currently report that HSR was composed of a tandem array of DM-derived sequences, which was shown using a unique DM-painting probe. Nevertheless, we found that HSR was replicated much later during the S phase, unless the amplified c-myc genes were expressed almost equally from DMs and HSR. Therefore, this provided a novel instance in which the cytogenetic localization affected replication timing without alteration of expression. Furthermore, we unexpectedly found that HSR had a distinctive band structure with respect to replication timing. The replication band structure was usually associated with the chromosomal G/R bands; however, HSR was homogeneous in the G/R band and in the distribution of highly repetitive sequences. We discuss the mechanism by which the replication band may arise, in relation to the folding of chromatin inside the nucleus.
许多人类癌细胞中的扩增基因通常定位于染色体外双微体(DMs)。在本研究中,我们发现人类结肠肿瘤COLO 320DM细胞系中的多个双微体在S期早期进行半同步复制。另一方面,在含有双微体的细胞传代时间延长时,染色体同源染色区(HSR)带有扩增基因的细胞通常在群体中占主导地位。我们目前报道,HSR由一系列串联的源自双微体的序列组成,这是通过一种独特的双微体荧光原位杂交探针证实的。然而,我们发现HSR在S期后期才进行复制,除非扩增的c-myc基因在双微体和HSR上的表达几乎相同。因此,这提供了一个新的例子,即细胞遗传学定位影响复制时间而不改变基因表达。此外,我们意外地发现HSR在复制时间方面具有独特的带型结构。复制带型结构通常与染色体的G/R带相关;然而,HSR在G/R带以及高度重复序列的分布上是均匀的。我们讨论了复制带可能产生的机制,这与细胞核内染色质的折叠有关。