Cuvier Olivier, Hirano Tatsuya
Cold Spring Harbor Laboratory, 1 Bungtown Rd., Cold Spring Harbor, NY 11724, USA.
J Cell Biol. 2003 Mar 3;160(5):645-55. doi: 10.1083/jcb.200209023. Epub 2003 Feb 25.
The condensin complex and topoisomerase II (topo II) have different biochemical activities in vitro, and both are required for mitotic chromosome condensation. We have used Xenopus egg extracts to investigate the functional interplay between condensin and topo II in chromosome condensation. When unreplicated chromatin is directly converted into chromosomes with single chromatids, the two proteins must function together, although they are independently targeted to chromosomes. In contrast, the requirement for topo II is temporarily separable from that of condensin when chromosome assembly is induced after DNA replication. This experimental setting allows us to find that, in the absence of condensin, topo II becomes enriched in an axial structure within uncondensed chromatin. Subsequent addition of condensin converts this structure into mitotic chromosomes in an ATP hydrolysis-dependent manner. Strikingly, preventing DNA replication by the addition of geminin or aphidicolin disturbs the formation of topo II-containing axes and alters the binding property of topo II with chromatin. Our results suggest that topo II plays an important role in an early stage of chromosome condensation, and that this function of topo II is tightly coupled with prior DNA replication.
凝聚素复合体和拓扑异构酶II(topo II)在体外具有不同的生化活性,二者都是有丝分裂染色体凝聚所必需的。我们利用非洲爪蟾卵提取物来研究凝聚素和topo II在染色体凝聚过程中的功能相互作用。当未复制的染色质直接转化为具有单条染色单体的染色体时,这两种蛋白质必须共同发挥作用,尽管它们是独立靶向染色体的。相比之下,当DNA复制后诱导染色体组装时,对topo II的需求与凝聚素的需求在时间上是可分离的。这种实验设置使我们发现,在没有凝聚素的情况下,topo II在未凝聚染色质的轴向结构中富集。随后添加凝聚素会以ATP水解依赖的方式将这种结构转化为有丝分裂染色体。引人注目的是,通过添加geminin或阿非迪霉素阻止DNA复制会干扰含topo II轴的形成,并改变topo II与染色质的结合特性。我们的结果表明,topo II在染色体凝聚的早期阶段发挥重要作用,并且topo II的这一功能与先前的DNA复制紧密相关。