Cell Cycle Laboratory, London Research Institute, Blanche Lane, Hertfordshire EN6 3LD, UK.
EMBO Rep. 2010 Apr;11(4):270-8. doi: 10.1038/embor.2010.27. Epub 2010 Feb 26.
Although the basic mechanisms of DNA synthesis are conserved across species, there are differences between simple and complex organisms. In contrast to lower eukaryotes, replication origins in complex eukaryotes lack DNA sequence specificity, can be activated in response to stressful conditions and require poorly conserved factors for replication firing. The response to replication fork damage is monitored by conserved proteins, such as the TIPIN-TIM-CLASPIN complex. The absence of this complex induces severe effects on yeast replication, whereas in higher eukaryotes it is only crucial when the availability of replication origins is limiting. Finally, the dependence of DNA replication on homologous recombination proteins such as RAD51 and the MRE11-RAD50-NBS1 complex is also different; they are dispensable for yeast S-phase but essential for accurate DNA replication in metazoans under unchallenged conditions. The reasons for these differences are not yet understood. Here, we focus on some of these known unknowns of DNA replication.
尽管 DNA 合成的基本机制在物种间是保守的,但简单和复杂生物之间存在差异。与低等真核生物不同,复杂真核生物的复制起点缺乏 DNA 序列特异性,可以响应应激条件而被激活,并需要较差保守的因子来启动复制。复制叉损伤的反应由保守蛋白监测,例如 TIPIN-TIM-CLASPIN 复合物。该复合物的缺失会对酵母复制产生严重影响,而在高等真核生物中,只有在复制起点的可用性受到限制时才至关重要。最后,DNA 复制对同源重组蛋白(如 RAD51 和 MRE11-RAD50-NBS1 复合物)的依赖性也不同;它们对酵母 S 期是可有可无的,但在未受挑战的条件下,对于后生动物中准确的 DNA 复制是必不可少的。这些差异的原因尚不清楚。在这里,我们专注于 DNA 复制的一些这些已知的未知。