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Replication in Hydroxyurea: It's a Matter of Time
Author(s) -
Gina M. Alvino,
David Collingwood,
J. M. Murphy,
Jeffrey J. Delrow,
Bonita J. Brewer,
M. K. Raghuraman
Publication year - 2007
Publication title -
molecular and cellular biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.14
H-Index - 327
eISSN - 1067-8824
pISSN - 0270-7306
DOI - 10.1128/mcb.00719-07
Subject(s) - biology , dna replication , replication (statistics) , origin recognition complex , replication timing , g2 m dna damage checkpoint , genome , control of chromosome duplication , origin of replication , genetics , pre replication complex , dna , licensing factor , microbiology and biotechnology , budding yeast , eukaryotic dna replication , saccharomyces cerevisiae , cell cycle , yeast , cell cycle checkpoint , gene , virology
Hydroxyurea (HU) is a DNA replication inhibitor that negatively affects both the elongation and initiation phases of replication and triggers the “intra-S phase checkpoint.” Previous work with budding yeast has shown that, during a short exposure to HU,MEC1/RAD53 prevent initiation at some late S phase origins. In this study, we have performed microarray experiments to follow the fate of all origins over an extended exposure to HU. We show that the genome-wide progression of DNA synthesis, including origin activation, follows the same pattern in the presence of HU as in its absence, although the time frames are very different. We find no evidence for a specific effect that excludes initiation from late origins. Rather, HU causes S phase to proceed in slow motion; all temporal classes of origins are affected, but the order in which they become active is maintained. We propose a revised model for the checkpoint response to HU that accounts for the continued but slowed pace of the temporal program of origin activation.

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