Gao Yanzhe, Yao Jianhong, Poudel Sumeet, Romer Eric, Abu-Niaaj Lubna, Leffak Michael
From the Department of Biochemistry and Molecular Biology, Boonshoft School of Medicine, Wright State University, Dayton, Ohio 45435.
From the Department of Biochemistry and Molecular Biology, Boonshoft School of Medicine, Wright State University, Dayton, Ohio 45435
J Biol Chem. 2014 Dec 26;289(52):35987-6000. doi: 10.1074/jbc.M114.589119. Epub 2014 Sep 25.
The DNA unwinding element (DUE)-binding protein (DUE-B) binds to replication origins coordinately with the minichromosome maintenance (MCM) helicase and the helicase activator Cdc45 in vivo, and loads Cdc45 onto chromatin in Xenopus egg extracts. Human DUE-B also retains the aminoacyl-tRNA proofreading function of its shorter orthologs in lower organisms. Here we report that phosphorylation of the DUE-B unstructured C-terminal domain unique to higher organisms regulates DUE-B intermolecular binding. Gel filtration analyses show that unphosphorylated DUE-B forms multiple high molecular weight (HMW) complexes. Several aminoacyl-tRNA synthetases and Mcm2-7 proteins were identified by mass spectrometry of the HMW complexes. Aminoacyl-tRNA synthetase binding is RNase A sensitive, whereas interaction with Mcm2-7 is nuclease resistant. Unphosphorylated DUE-B HMW complex formation is decreased by PP2A inhibition or direct DUE-B phosphorylation, and increased by inhibition of Cdc7. These results indicate that the state of DUE-B phosphorylation is maintained by the equilibrium between Cdc7-dependent phosphorylation and PP2A-dependent dephosphorylation, each previously shown to regulate replication initiation. Alanine mutation of the DUE-B C-terminal phosphorylation target sites increases MCM binding but blocks Cdc45 loading in vivo and inhibits cell division. In egg extracts alanine mutation of the DUE-B C-terminal phosphorylation sites blocks Cdc45 loading and inhibits DNA replication. The effects of DUE-B C-terminal phosphorylation reveal a novel S phase kinase regulatory mechanism for Cdc45 loading and MCM helicase activation.
DNA解旋元件(DUE)结合蛋白(DUE-B)在体内与微型染色体维持(MCM)解旋酶和解旋酶激活因子Cdc45协同结合到复制起点,并在非洲爪蟾卵提取物中将Cdc45加载到染色质上。人类DUE-B还保留了其在低等生物中较短同源物的氨酰tRNA校对功能。在此我们报告,高等生物特有的DUE-B非结构化C末端结构域的磷酸化调节DUE-B分子间结合。凝胶过滤分析表明,未磷酸化的DUE-B形成多种高分子量(HMW)复合物。通过对HMW复合物进行质谱分析鉴定出了几种氨酰tRNA合成酶和Mcm2-7蛋白。氨酰tRNA合成酶的结合对RNase A敏感,而与Mcm2-7的相互作用对核酸酶具有抗性。PP2A抑制或直接对DUE-B进行磷酸化会减少未磷酸化的DUE-B HMW复合物的形成,而抑制Cdc7则会增加其形成。这些结果表明,DUE-B磷酸化状态由Cdc7依赖性磷酸化和PP2A依赖性去磷酸化之间的平衡维持,此前已证明二者均可调节复制起始。DUE-B C末端磷酸化靶位点的丙氨酸突变增加了MCM结合,但在体内阻断了Cdc45加载并抑制了细胞分裂。在卵提取物中,DUE-B C末端磷酸化位点的丙氨酸突变阻断了Cdc45加载并抑制了DNA复制。DUE-B C末端磷酸化的作用揭示了一种用于Cdc45加载和MCM解旋酶激活的新型S期激酶调节机制。