Program in Molecular Biology and Memorial Sloan-Kettering Cancer Center, New York, New York 10065.
Department of Medicine, Memorial Sloan-Kettering Cancer Center, New York, New York 10065.
J Biol Chem. 2014 Oct 31;289(44):30810-30821. doi: 10.1074/jbc.M114.552935. Epub 2014 Sep 17.
The initial step in initiation of eukaryotic DNA replication involves the assembly of pre-replicative complexes (pre-RCs) at origins of replication during the G1 phase of the cell cycle. In metazoans initiation is inhibited by the regulatory factor Geminin. We have purified the human pre-RC proteins, studied their interactions in vitro with each other and with origin DNA, and analyzed the effects of HsGeminin on formation of DNA-protein complexes. The formation of an initial complex containing the human origin recognition complex (HsORC), HsCdt1, HsCdc6, and origin DNA is cooperative, involving all possible binary interactions among the components. Maximal association of HsMCM2-7, a component of the replicative helicase, requires HsORC, HsCdc6, HsCdt1, and ATP, and is driven by interactions of HsCdt1 and HsCdc6 with multiple HsMCM2-7 subunits. Formation of stable complexes, resistant to high salt, requires ATP hydrolysis. In the absence of HsMCM proteins, HsGeminin inhibits the association of HsCdt1 with DNA or with HsORC-HsCdc6-DNA complexes. However, HsGeminin does not inhibit recruitment of HsMCM2-7 to DNA to form complexes containing all of the pre-RC proteins. In fact, HsGeminin itself is a component of such complexes, and interacts directly with the HsMcm3 and HsMcm5 subunits of HsMCM2-7, as well as with HsCdt1. Although HsGeminin does not prevent the initial formation of DNA-protein complexes containing the pre-RC proteins, it strongly inhibits the formation of stable pre-RCs that are resistant to high salt. We suggest that bound HsGeminin prevents transition of the pre-RC to a state that is competent for initiation of DNA replication.
真核生物 DNA 复制的起始步骤涉及在细胞周期的 G1 期在复制起点处组装复制前复合物(pre-RC)。在后生动物中,起始被调节因子 Geminin 抑制。我们已经纯化了人 pre-RC 蛋白,研究了它们在体外相互之间以及与起源 DNA 的相互作用,并分析了 HsGeminin 对 DNA-蛋白复合物形成的影响。包含人起始识别复合物(HsORC)、HsCdt1、HsCdc6 和起源 DNA 的初始复合物的形成是合作的,涉及到各组分之间所有可能的二元相互作用。人复制解旋酶的一个组成部分 HsMCM2-7 的最大缔合需要 HsORC、HsCdc6、HsCdt1 和 ATP,并且由 HsCdt1 和 HsCdc6 与多个 HsMCM2-7 亚基的相互作用驱动。形成稳定的复合物,抵抗高盐,需要 ATP 水解。在没有 HsMCM 蛋白的情况下,HsGeminin 抑制 HsCdt1 与 DNA 或与 HsORC-HsCdc6-DNA 复合物的结合。然而,HsGeminin 并不抑制 HsMCM2-7 招募到 DNA 上形成包含所有 pre-RC 蛋白的复合物。事实上,HsGeminin 本身就是这种复合物的一个组成部分,它直接与 HsMcm3 和 HsMcm5 亚基相互作用,以及与 HsCdt1 相互作用。尽管 HsGeminin 不阻止包含 pre-RC 蛋白的 DNA-蛋白复合物的初始形成,但它强烈抑制形成对高盐具有抗性的稳定 pre-RC。我们认为,结合的 HsGeminin 阻止 pre-RC 向具有 DNA 复制起始能力的状态转变。