Department of Biology, Technische Universität Darmstadt, Germany.
Cold Spring Harb Perspect Biol. 2010 Apr;2(4):a000737. doi: 10.1101/cshperspect.a000737.
The discovery of the DNA double helix structure half a century ago immediately suggested a mechanism for its duplication by semi-conservative copying of the nucleotide sequence into two DNA daughter strands. Shortly after, a second fundamental step toward the elucidation of the mechanism of DNA replication was taken with the isolation of the first enzyme able to polymerize DNA from a template. In the subsequent years, the basic mechanism of DNA replication and its enzymatic machinery components were elucidated, mostly through genetic approaches and in vitro biochemistry. Most recently, the spatial and temporal organization of the DNA replication process in vivo within the context of chromatin and inside the intact cell are finally beginning to be elucidated. On the one hand, recent advances in genome-wide high throughput techniques are providing a new wave of information on the progression of genome replication at high spatial resolution. On the other hand, novel super-resolution microscopy techniques are just starting to give us the first glimpses of how DNA replication is organized within the context of single intact cells with high spatial resolution. The integration of these data with time lapse microscopy analysis will give us the ability to film and dissect the replication of the genome in situ and in real time.
半个世纪前 DNA 双螺旋结构的发现,立即为其通过核苷酸序列半保守复制到两条 DNA 子链的机制提供了一种解释。此后不久,通过分离出第一种能够从模板聚合 DNA 的酶,朝着阐明 DNA 复制机制的第二个基本步骤迈进。在随后的几年里,通过遗传方法和体外生物化学,阐明了 DNA 复制的基本机制及其酶学机制成分。最近,在染色质和完整细胞内的背景下,体内 DNA 复制过程的时空组织终于开始被阐明。一方面,全基因组高通量技术的最新进展为在高空间分辨率下研究基因组复制的进展提供了一波新的信息。另一方面,新型超分辨率显微镜技术才刚刚开始让我们初步了解 DNA 复制在单个完整细胞内的组织情况,具有很高的空间分辨率。将这些数据与延时显微镜分析相结合,将使我们能够实时原位拍摄和剖析基因组的复制。