Gerhardt Jeannine, Guler Gulfem D, Fanning Ellen
Department of Cell Biology, Albert Einstein College of Medicine, Bronx, NY 10461, USA.
Department of Biological Sciences, Vanderbilt University, Nashville, TN 37235, USA.
Exp Cell Res. 2015 Jun 10;334(2):283-93. doi: 10.1016/j.yexcr.2015.04.014. Epub 2015 Apr 29.
The chromosomal DNA replication in eukaryotic cells begins at replication initation sites, which are marked by the assembly of the pre-replication complexes in early G1. At the G1/S transition, recruitment of additional replication initiation proteins enables origin DNA unwinding and loading of DNA polymerases. We found that depletion of the human DNA helicase B (HDHB) inhibits the initiation of DNA replication, suggesting a role of HDHB in the beginning of the DNA synthesis. To gain insight into the function of HDHB during replication initiation, we examined the physical interactions of purified recombinant HDHB with key initiation proteins. HDHB interacts directly with two initiation factors TopBP1 and Cdc45. In addition we found that both, the N-terminus and helicase domain of HDHB bind to the N-terminus of Cdc45. Furthermore depletion of HDHB from human cells diminishes Cdc45 association with chromatin, suggesting that HDHB may facilitate Cdc45 recruitment at G1/S in human cells.
真核细胞中的染色体DNA复制始于复制起始位点,这些位点在G1早期由前复制复合体的组装标记。在G1/S转换时,招募额外的复制起始蛋白可使起始点DNA解旋并加载DNA聚合酶。我们发现,人类DNA解旋酶B(HDHB)的缺失会抑制DNA复制的起始,这表明HDHB在DNA合成起始过程中发挥作用。为深入了解HDHB在复制起始过程中的功能,我们检测了纯化的重组HDHB与关键起始蛋白的物理相互作用。HDHB直接与两个起始因子TopBP1和Cdc45相互作用。此外,我们发现HDHB的N端和解旋酶结构域都与Cdc45的N端结合。此外,从人类细胞中去除HDHB会减少Cdc45与染色质的结合,这表明HDHB可能在人类细胞的G1/S期促进Cdc45的招募。