Department of Biochemistry, Oxford University, South Parks Road, Oxford, OX1 3QU, UK.
Department of Cell Biology, the Netherlands Cancer Institute, Plesmanlaan 121, 1066 CX Amsterdam, the Netherlands.
Cell Rep. 2017 Sep 19;20(12):2749-2755. doi: 10.1016/j.celrep.2017.08.092.
To ensure disjunction to opposite poles during anaphase, sister chromatids must be held together following DNA replication. This is mediated by cohesin, which is thought to entrap sister DNAs inside a tripartite ring composed of its Smc and kleisin (Scc1) subunits. How such structures are created during S phase is poorly understood, in particular whether they are derived from complexes that had entrapped DNAs prior to replication. To address this, we used selective photobleaching to determine whether cohesin associated with chromatin in G1 persists in situ after replication. We developed a non-fluorescent HaloTag ligand to discriminate the fluorescence recovery signal from labeling of newly synthesized Halo-tagged Scc1 protein (pulse-chase or pcFRAP). In cells where cohesin turnover is inactivated by deletion of WAPL, Scc1 can remain associated with chromatin throughout S phase. These findings suggest that cohesion might be generated by cohesin that is already bound to un-replicated DNA.
为确保在后期中到两极的分离,姐妹染色单体在 DNA 复制后必须保持在一起。这是由黏合蛋白介导的,黏合蛋白被认为将姐妹 DNA 困在由其 Smc 和 kleisin(Scc1)亚基组成的三部分环内。在 S 期期间如何形成这种结构尚不清楚,特别是它们是否来自于在复制之前已困住 DNA 的复合物。为了解决这个问题,我们使用选择性光漂白来确定在复制后 G1 期与染色质结合的黏合蛋白是否仍然存在于原位。我们开发了一种非荧光 HaloTag 配体,以区分新合成的 Halo 标记的 Scc1 蛋白(脉冲追踪或 pcFRAP)的荧光恢复信号。在通过删除 WAPL 使黏合蛋白周转失活的细胞中,Scc1 可以在整个 S 期与染色质保持关联。这些发现表明,黏合可能是由已经结合未复制 DNA 的黏合蛋白产生的。