Schwob Etienne
Institute of Molecular Genetics, CNRS UMR5535 and University Montpellier 2, 1919, route de Mende, 34293 Montpellier, France.
Curr Opin Microbiol. 2004 Dec;7(6):680-90. doi: 10.1016/j.mib.2004.10.017.
Eukaryotic DNA replication begins at numerous but often poorly characterized sequences called origins, which are distributed fairly regularly along chromosomes. The elusive and idiosyncratic nature of origins in higher eukaryotes is now understood as resulting from a strong epigenetic influence on their specification, which provides flexibility in origin selection and allows for tailoring the dynamics of chromosome replication to the specific needs of cells. By contrast, the factors that assemble in trans to make these origins competent for replication and the kinases that trigger initiation are well conserved. Genome-wide and single-molecule approaches are being developed to elucidate the dynamics of chromosome replication. The notion that a well-coordinated progression of replication forks is crucial for many aspects of the chromosome cycle besides simply duplication begins to be appreciated.
真核生物的DNA复制始于众多但通常特征不明的序列,即所谓的起点,这些起点沿染色体分布相当规律。高等真核生物中起点难以捉摸且具有特异性的本质,现在被认为是由于对其指定产生强烈的表观遗传影响所致,这在起点选择上提供了灵活性,并允许根据细胞的特定需求调整染色体复制的动态过程。相比之下,反式组装以使这些起点具有复制能力的因子以及触发起始的激酶则高度保守。正在开发全基因组和单分子方法来阐明染色体复制的动态过程。人们开始认识到,复制叉的协调进展对于染色体循环的许多方面至关重要,而不仅仅是简单的复制。