Department of Biological Sciences, Vanderbilt University, Nashville, United States.
Department of Medicine, Vanderbilt University School of Medicine, Nashville, United States.
Elife. 2018 Oct 2;7:e39140. doi: 10.7554/eLife.39140.
Control of DNA copy number is essential to maintain genome stability and ensure proper cell and tissue function. In polyploid cells, the SNF2-domain-containing SUUR protein inhibits replication fork progression within specific regions of the genome to promote DNA underreplication. While dissecting the function of SUUR's SNF2 domain, we identified an interaction between SUUR and Rif1. Rif1 has many roles in DNA metabolism and regulates the replication timing program. We demonstrate that repression of DNA replication is dependent on Rif1. Rif1 localizes to active replication forks in a partially SUUR-dependent manner and directly regulates replication fork progression. Importantly, SUUR associates with replication forks in the absence of Rif1, indicating that Rif1 acts downstream of SUUR to inhibit fork progression. Our findings uncover an unrecognized function of the Rif1 protein as a regulator of replication fork progression.
控制 DNA 拷贝数对于维持基因组稳定性和确保细胞和组织功能正常至关重要。在多倍体细胞中,含有 SNF2 结构域的 SUUR 蛋白抑制基因组特定区域内的复制叉前进,以促进 DNA 复制不足。在解析 SUUR 的 SNF2 结构域功能时,我们发现 SUUR 与 Rif1 之间存在相互作用。 Rif1 在 DNA 代谢中具有多种功能,并调节复制起始程序。我们证明 DNA 复制的抑制依赖于 Rif1。 Rif1 以部分依赖于 SUUR 的方式定位于活跃的复制叉上,并直接调节复制叉的前进。重要的是,在没有 Rif1 的情况下,SUUR 与复制叉结合,表明 Rif1 作为复制叉前进的抑制剂,作用于 SUUR 的下游。我们的研究结果揭示了 Rif1 蛋白作为复制叉前进的调节剂的一个未被识别的功能。