Dulev Stanimir, Aragon Luis, Strunnikov Alexander
Laboratory of Gene Regulation and Development, National Institute of Child Health and Human Development, Bethesda, MD 20892, USA.
Front Biosci. 2008 May 1;13:5838-46. doi: 10.2741/3120.
Condensin is the core activity responsible for chromosome condensation in mitosis. In the yeast S. cerevisiae, condensin binding is enriched at the regions where DNA replication terminates. Therefore, we investigated whether DNA replication completion determines the condensin-binding proficiency of chromatin. In order to fulfill putative mitotic requirements for condensin activity we analyzed chromosome condensation and condensin binding to unreplicated chromosomes in mitosis. For this purpose we used pGAL:CDC6 cdc15-ts cells that are known to enter mitosis without DNA replication if CDC6 transcription is repressed prior to S-phase. Both the condensation of nucleolar chromatin and proper condensin targeting to rDNA sites failed when unreplicated chromosomes were driven in mitosis. We propose that the DNA replication results in structural and/or biochemical changes to replicated chromatin, which are required for two-phase condensin binding and proper chromosome condensation.
凝聚素是有丝分裂中负责染色体凝聚的核心活性物质。在酿酒酵母中,凝聚素结合在DNA复制终止的区域富集。因此,我们研究了DNA复制的完成是否决定了染色质对凝聚素的结合能力。为了满足对凝聚素活性假定的有丝分裂需求,我们分析了有丝分裂中染色体凝聚以及凝聚素与未复制染色体的结合情况。为此,我们使用了pGAL:CDC6 cdc15-ts细胞,如果在S期之前抑制CDC6转录,已知这些细胞会在没有DNA复制的情况下进入有丝分裂。当未复制的染色体进入有丝分裂时,核仁染色质的凝聚以及凝聚素正确靶向rDNA位点均失败。我们提出,DNA复制导致复制染色质发生结构和/或生化变化,这是凝聚素两阶段结合和正确染色体凝聚所必需的。