Vertebrate DNA Replication Lab, Centre for Medical Biotechnology, University of Duisburg-Essen, Essen, Germany.
Medical Research Council Human Genetics Unit, IGMM, University of Edinburgh, Edinburgh, Scotland, United Kingdom.
PLoS Biol. 2019 Jan 29;17(1):e2006767. doi: 10.1371/journal.pbio.2006767. eCollection 2019 Jan.
Accurate genome duplication underlies genetic homeostasis. Metazoan Mdm2 binding protein (MTBP) forms a main regulatory platform for origin firing together with Treslin/TICRR and TopBP1 (Topoisomerase II binding protein 1 (TopBP1)-interacting replication stimulating protein/TopBP1-interacting checkpoint and replication regulator). We report the first comprehensive analysis of MTBP and reveal conserved and metazoa-specific MTBP functions in replication. This suggests that metazoa have evolved specific molecular mechanisms to adapt replication principles conserved with yeast to the specific requirements of the more complex metazoan cells. We uncover one such metazoa-specific process: a new replication factor, cyclin-dependent kinase 8/19-cyclinC (Cdk8/19-cyclin C), binds to a central domain of MTBP. This interaction is required for complete genome duplication in human cells. In the absence of MTBP binding to Cdk8/19-cyclin C, cells enter mitosis with incompletely duplicated chromosomes, and subsequent chromosome segregation occurs inaccurately. Using remote homology searches, we identified MTBP as the metazoan orthologue of yeast synthetic lethal with Dpb11 7 (Sld7). This homology finally demonstrates that the set of yeast core factors sufficient for replication initiation in vitro is conserved in metazoa. MTBP and Sld7 contain two homologous domains that are present in no other protein, one each in the N and C termini. In MTBP the conserved termini flank the metazoa-specific Cdk8/19-cyclin C binding region and are required for normal origin firing in human cells. The N termini of MTBP and Sld7 share an essential origin firing function, the interaction with Treslin/TICRR or its yeast orthologue Sld3, respectively. The C termini may function as homodimerisation domains. Our characterisation of broadly conserved and metazoa-specific initiation processes sets the basis for further mechanistic dissection of replication initiation in vertebrates. It is a first step in understanding the distinctions of origin firing in higher eukaryotes.
精确的基因组复制是遗传稳定性的基础。真核生物 Mdm2 结合蛋白 (MTBP) 与 Treslin/TICRR 和 TopBP1(拓扑异构酶 II 结合蛋白 1 (TopBP1)-相互作用的复制刺激蛋白/TopBP1 相互作用的检查点和复制调节剂)一起形成主要的调控平台,用于启动复制原点。我们报告了对 MTBP 的首次全面分析,并揭示了 MTBP 在复制中的保守和特定于后生动物的功能。这表明后生动物已经进化出特定的分子机制,将与酵母保守的复制原理适应于更复杂的后生动物细胞的特定要求。我们揭示了一个这样的后生动物特异性过程:一种新的复制因子,细胞周期蛋白依赖性激酶 8/19-细胞周期蛋白 C(Cdk8/19-cyclin C),与 MTBP 的中心结构域结合。这种相互作用是人类细胞中完成基因组复制所必需的。在没有 MTBP 与 Cdk8/19-cyclin C 结合的情况下,细胞进入有丝分裂时染色体复制不完全,随后的染色体分离也不准确。通过远程同源搜索,我们将 MTBP 鉴定为酵母合成致死与 Dpb11 7(Sld7)的后生动物直系同源物。这种同源性最终证明了在体外复制起始中足够的酵母核心因子集合在后生动物中是保守的。MTBP 和 Sld7 包含两个同源结构域,这些结构域不存在于其他任何蛋白质中,分别位于 N 和 C 末端。在 MTBP 中,保守的末端侧翼是后生动物特异性的 Cdk8/19-cyclin C 结合区域,并且对于人类细胞中的正常起始原点是必需的。MTBP 和 Sld7 的 N 末端分别具有与 Treslin/TICRR 或其酵母直系同源物 Sld3 的必需起始原点功能相互作用。C 末端可能作为同源二聚化结构域发挥作用。我们对广泛保守和特定于后生动物的起始过程的描述为进一步深入研究脊椎动物的复制起始奠定了基础。这是理解高等真核生物起始原点功能差异的第一步。