Zegerman Philip, Diffley John F X
Cancer Research UK London Research Institute, Clare Hall Laboratories, South Mimms, Hertfordshire EN6 3LD, UK.
Nature. 2007 Jan 18;445(7125):281-5. doi: 10.1038/nature05432. Epub 2006 Dec 13.
Cyclin-dependent kinases (CDKs) drive major cell cycle events including the initiation of chromosomal DNA replication. We identified two S phase CDK (S-CDK) phosphorylation sites in the budding yeast Sld3 protein that, together, are essential for DNA replication. Here we show that, when phosphorylated, these sites bind to the amino-terminal BRCT repeats of Dpb11. An Sld3-Dpb11 fusion construct bypasses the requirement for both Sld3 phosphorylation and the N-terminal BRCT repeats of Dpb11. Co-expression of this fusion with a phospho-mimicking mutant in a second essential CDK substrate, Sld2, promotes DNA replication in the absence of S-CDK. Therefore, Sld2 and Sld3 are the minimal set of S-CDK targets required for DNA replication. DNA replication in cells lacking G1 phase CDK (G1-CDK) required expression of the Cdc7 kinase regulatory subunit, Dbf4, as well as Sld2 and Sld3 bypass. Our results help to explain how G1- and S-CDKs promote DNA replication in yeast.
细胞周期蛋白依赖性激酶(CDK)驱动包括染色体DNA复制起始在内的主要细胞周期事件。我们在芽殖酵母Sld3蛋白中鉴定出两个S期CDK(S-CDK)磷酸化位点,这两个位点共同对DNA复制至关重要。在此我们表明,磷酸化后,这些位点与Dpb11的氨基末端BRCT重复序列结合。一个Sld3-Dpb11融合构建体绕过了对Sld3磷酸化和Dpb11氨基末端BRCT重复序列的需求。该融合体与第二个必需的CDK底物Sld2中的磷酸模拟突变体共表达,可在无S-CDK的情况下促进DNA复制。因此,Sld2和Sld3是DNA复制所需的最小一组S-CDK靶标。缺乏G1期CDK(G1-CDK)的细胞中的DNA复制需要Cdc7激酶调节亚基Dbf4的表达以及Sld2和Sld3的旁路。我们的结果有助于解释G1-CDK和S-CDK如何促进酵母中的DNA复制。