4D Visualization of replication foci in mammalian cells corresponding to individual replicons

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 im...

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Veröffentlicht in:Nature communications 2016-04, Vol.7 (1), p.11231-11231, Article 11231
Hauptverfasser: Chagin, V. O., Casas-Delucchi, C. S., Reinhart, M., Schermelleh, L., Markaki, Y., Maiser, A., Bolius, J. J., Bensimon, A., Fillies, M., Domaing, P., Rozanov, Y. M., Leonhardt, H., Cardoso, M. C.
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Sprache:eng
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Zusammenfassung: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. Whether replication happens at individual replicons or in replication factories is a controversial debate. Here the authors use super-resolution microscopy and analysis of replication fork speed to present evidence in favour of replicons.
ISSN:2041-1723
2041-1723
DOI:10.1038/ncomms11231