Vadim O. Chagin1, Jeffrey H. Stear2 and M. Cristina Cardoso1
-Author Affiliations
1Department of Biology, Technische Universität Darmstadt, 64287 Darmstadt, Germany
2Institute for Biology, Humboldt University, 10115 Berlin, Germany
Correspondence:cardoso@bio.tu-darmstadt.de
Abstract
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.
Copyright © 2010 Cold Spring Harbor Laboratory Press; all rights reserved
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