Since the pioneering proposal of the replicon model of DNA replication 50
years ago, the predicted replicons have not been identified and quantified at
the cellular level. Here, we combine conventional and super-resolution
microscopy of replication sites in live and fixed cells with computational
image analysis. We complement these data with genome size measurements,
comprehensive analysis of S-phase dynamics and quantification of replication
fork speed and replicon size in human and mouse cells. These multidimensional
analyses demonstrate that replication foci (RFi) in three-dimensional (3D)
preserved somatic mammalian cells can be optically resolved down to single
replicons throughout S-phase. This challenges the conventional interpretation
of nuclear RFi as replication factories, that is, the complex entities that
process multiple clustered replicons. Accordingly, 3D genome organization and
duplication can be now followed within the chromatin context at the level of
individual replicons