Yamada Yoshiki, Nakagawa Takuro, Masukata Hisao
Graduate School of Science, Osaka University, Osaka 560-0043 Japan.
Mol Biol Cell. 2004 Aug;15(8):3740-50. doi: 10.1091/mbc.e04-04-0292. Epub 2004 Jun 11.
Assembly of initiation factors on individual replication origins at onset of S phase is crucial for regulation of replication timing and repression of initiation by S-phase checkpoint control. We dissected the process of preinitiation complex formation using a point mutation in fission yeast nda4-108/mcm5 that shows tight genetic interactions with sna41(+)/cdc45(+). The mutation does not affect loading of MCM complex onto origins, but impairs Cdc45-loading, presumably because of a defect in interaction of MCM with Cdc45. In the mcm5 mutant, however, Sld3, which is required for Cdc45-loading, proficiently associates with origins. Origin-association of Sld3 without Cdc45 is also observed in the sna41/cdc45 mutant. These results suggest that Sld3-loading is independent of Cdc45-loading, which is different from those observed in budding yeast. Interestingly, returning the arrested mcm5 cells to the permissive temperature results in immediate loading of Cdc45 to the origin and resumption of DNA replication. These results suggest that the complex containing MCM and Sld3 is an intermediate for initiation of DNA replication in fission yeast.
在S期开始时,起始因子在各个复制起点上的组装对于复制时间的调控以及S期检查点控制对起始的抑制至关重要。我们利用裂殖酵母nda4-108/mcm5中的一个点突变来剖析起始前复合物形成的过程,该突变与sna41(+)/cdc45(+)表现出紧密的遗传相互作用。该突变不影响MCM复合物加载到起点上,但会损害Cdc45的加载,推测是由于MCM与Cdc45相互作用存在缺陷。然而,在mcm5突变体中,Cdc45加载所需的Sld3能有效地与起点结合。在sna41/cdc45突变体中也观察到没有Cdc45时Sld3与起点的结合。这些结果表明Sld3的加载独立于Cdc45的加载,这与在芽殖酵母中观察到的情况不同。有趣的是,将停滞的mcm5细胞恢复到允许温度会导致Cdc45立即加载到起点并恢复DNA复制。这些结果表明,含有MCM和Sld3的复合物是裂殖酵母中DNA复制起始的中间体。