Structural Biology of Chromosome Segregation Laboratory, The Francis Crick Institute, 1 Midland Road, London NW1 1AT, UK.
Chromosome Segregation Laboratory, The Francis Crick Institute, 1 Midland Road, London NW1 1AT, UK.
Nat Commun. 2017 Jan 6;8:13952. doi: 10.1038/ncomms13952.
The functions of cohesin are central to genome integrity, chromosome organization and transcription regulation through its prevention of premature sister-chromatid separation and the formation of DNA loops. The loading of cohesin onto chromatin depends on the Scc2-Scc4 complex; however, little is known about how it stimulates the cohesion-loading activity. Here we determine the large 'hook' structure of Scc2 responsible for catalysing cohesin loading. We identify key Scc2 surfaces that are crucial for cohesin loading in vivo. With the aid of previously determined structures and homology modelling, we derive a pseudo-atomic structure of the full-length Scc2-Scc4 complex. Finally, using recombinantly purified Scc2-Scc4 and cohesin, we performed crosslinking mass spectrometry and interaction assays that suggest Scc2-Scc4 uses its modular structure to make multiple contacts with cohesin.
着丝粒蛋白的功能对于基因组完整性、染色体组织和转录调控至关重要,它可以防止姐妹染色单体过早分离,并形成 DNA 环。着丝粒蛋白在染色质上的加载依赖于 Scc2-Scc4 复合物;然而,对于它如何刺激着丝粒蛋白加载活性知之甚少。在这里,我们确定了 Scc2 负责催化着丝粒蛋白加载的大“钩”结构。我们鉴定了体内着丝粒蛋白加载所必需的关键 Scc2 表面。借助先前确定的结构和同源建模,我们推导出了全长 Scc2-Scc4 复合物的拟原子结构。最后,使用重组纯化的 Scc2-Scc4 和着丝粒蛋白,我们进行了交联质谱和相互作用分析,表明 Scc2-Scc4 利用其模块化结构与着丝粒蛋白形成多种相互作用。