Chevalier S, Tassan J P, Cox R, Philippe M, Ford C
Département de Biologie et Génétique du Développement, CNRS, URA 256, Université de Rennes I, France.
J Cell Sci. 1995 May;108 ( Pt 5):1831-41. doi: 10.1242/jcs.108.5.1831.
Xenopus egg extracts induce S phase DNA replication in added sperm pronuclei in a highly regulated manner, similar to events in vivo. Removal of cyclin-dependant kinases (cdks) or cdk2 from these extracts using affinity matrices severely inhibits initiation of S phase. We have used p13suc1 beads to remove both cdk2 and cdc2 proteins from egg extracts and developed a method to replace either protein alone to assess their capacity to initiate DNA replication. Re-addition of either cdk2 or cdc2 proteins to depleted extracts, through translation of their respective mRNAs, restimulated replication, judged by both total synthesis and labelling index. An ATP-binding-site mutant cdk2 mRNA (cdk2.R33) failed to stimulate replication and inhibited S phase initiation in mock-depleted extracts. Both human and Xenopus cdc2 mRNAs rescued replication in this system. Human mutant mRNAs have been used to show that the stimulation induced requires cdc2 catalytic activity, though not its mitotically active form. Rescue of replication by p34cdc2 is also observed in extracts depleted of cdks with a cdk2 antibody, which still retain much of their endogenous cdc2 protein. We conclude that newly synthesised p34cdc2, but not the inherited 'old' form, can induce S phase and in this form may overlap in function with p33cdk2.
非洲爪蟾卵提取物能以高度调控的方式诱导添加的精子原核进入S期DNA复制,这类似于体内发生的事件。使用亲和基质从这些提取物中去除细胞周期蛋白依赖性激酶(cdks)或cdk2会严重抑制S期的起始。我们已使用p13suc1珠从卵提取物中去除cdk2和cdc2蛋白,并开发了一种方法来单独替换其中任何一种蛋白,以评估它们启动DNA复制的能力。通过各自mRNA的翻译将cdk2或cdc2蛋白重新添加到耗尽的提取物中,从总合成和标记指数来看,重新刺激了复制。一种ATP结合位点突变的cdk2 mRNA(cdk2.R33)未能刺激复制,并在模拟耗尽的提取物中抑制S期起始。人和非洲爪蟾的cdc2 mRNA都能在该系统中挽救复制。已使用人类突变mRNA表明,诱导的刺激需要cdc2催化活性,尽管不是其有丝分裂活性形式。在用cdk2抗体耗尽cdks的提取物中也观察到p34cdc2对复制的挽救,这些提取物仍保留许多内源性cdc2蛋白。我们得出结论,新合成的p34cdc2而非遗传的“旧”形式可以诱导S期,并且这种形式在功能上可能与p33cdk2重叠。