Murakami H, Nurse P
Cell Cycle Laboratory, Imperial Cancer Research Fund, 44 Lincoln's Inn Fields, London WC2A 3PX, UK.
Nat Genet. 2001 Jul;28(3):290-3. doi: 10.1038/90142.
The meiotic cell cycle is characterized by high levels of recombination induced by DNA double-strand breaks (DSBs), which appear after completion of premeiotic S phase, leading to the view that initiation of recombination depends on meiotic DNA replication. It has also been indicated that DNA replication initiation proteins may differ between the meiotic and mitotic cell cycles, giving rise to an altered S phase, which could contribute to the high level of recombination during meiosis. We have investigated these possibilities in the fission yeast Schizosaccharomyces pombe and found that core DNA replication initiation proteins used during the mitotic cell cycle, including Cdc18p (budding yeast Cdc6p), Cdc19p (Mcm2p), Cdc21p (Mcm4p) and Orp1p (Orc1p), are also required for premeiotic S phase. Reduced activity of these proteins prevents completion of DNA replication but not formation of DSBs. We conclude that recombination-related DSB formation does not depend on the completion of meiotic DNA replication and we propose two parallel developmental sequences during the meiotic cell cycle: one for premeiotic S phase and the other for initiating recombination.
减数分裂细胞周期的特点是由DNA双链断裂(DSB)诱导的高水平重组,这些双链断裂在减数分裂前S期完成后出现,这导致了一种观点,即重组的起始依赖于减数分裂DNA复制。也有研究表明,减数分裂和有丝分裂细胞周期中的DNA复制起始蛋白可能不同,从而导致S期发生改变,这可能有助于减数分裂期间的高水平重组。我们在裂殖酵母粟酒裂殖酵母中研究了这些可能性,发现有丝分裂细胞周期中使用的核心DNA复制起始蛋白,包括Cdc18p(芽殖酵母Cdc6p)、Cdc19p(Mcm2p)、Cdc21p(Mcm4p)和Orp1p(Orc1p),在减数分裂前S期也是必需的。这些蛋白活性的降低会阻止DNA复制的完成,但不会阻止DSB的形成。我们得出结论,与重组相关的DSB形成不依赖于减数分裂DNA复制的完成,并且我们提出在减数分裂细胞周期中有两个平行的发育序列:一个用于减数分裂前S期,另一个用于启动重组。