Université Pierre et Marie Curie-Paris6, Laboratoire Arago, Banyuls-sur-mer, BP44, Avenue du Fontaulé, F-66651, France.
Dev Biol. 2010 Apr 15;340(2):557-70. doi: 10.1016/j.ydbio.2010.02.009. Epub 2010 Feb 11.
Fertilization relieves the oocyte from a cell cycle arrest, inducing progression towards mitotic cycles. While the signalling pathways involved in oocyte to embryo transition have been widely investigated, how they specifically trigger DNA replication is still unclear. We used sea urchin eggs whose oocytes are arrested in G1 to investigate in vivo the molecular mechanisms regulating initiation of replication after fertilization. Unexpectedly, we found that CDC6, Cdt1 and MCM3, components of the pre-replication complexes (pre-RC) which license origins for replication, were already loaded on female chromatin before fertilization. This is the first demonstration of a cell cycle arrest in metazoan in which chromatin is already licensed for replication. In contrast pre-RC assemble on chromatin post-fertilization as in other organisms. These differences in the timing of pre-RC assembly are accompanied by differences in Cdk2 requirement for DNA replication initiation between female and male chromatin post-fertilization. Finally, we demonstrated that a concomitant inhibition of MAP kinase and ATM/ATR pathways releases the block to DNA synthesis. Our findings provide new insight into the mechanisms contributing to the release of G1 arrest and the control of S-phase entry at fertilization.
受精使卵母细胞从细胞周期阻滞中解脱出来,促使其向有丝分裂周期推进。虽然卵母细胞向胚胎过渡过程中涉及的信号通路已被广泛研究,但它们如何特异性地触发 DNA 复制仍不清楚。我们使用海胆卵,其卵母细胞在 G1 期被阻滞,以体内方式研究受精后复制起始的调控分子机制。出乎意料的是,我们发现,CDC6、Cdt1 和 MCM3,即预复制复合物(pre-RC)的组成部分,在受精前就已经加载到雌性染色质上了。这是在多细胞动物中首次证明染色质在细胞周期阻滞时已经获得了复制许可。相比之下,在其他生物中,pre-RC 是在受精后组装在染色质上的。这些 pre-RC 组装时间上的差异伴随着受精后雌性和雄性染色质中 CDK2 对 DNA 复制起始的需求不同。最后,我们证明了同时抑制 MAP 激酶和 ATM/ATR 途径可以释放 DNA 合成的阻滞。我们的研究结果为阐明 G1 阻滞的释放机制以及控制受精时 S 期进入提供了新的认识。