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dc.contributor.authorTYSON, CJen_US
dc.contributor.authorMarlovits, Gen_US
dc.contributor.authorNovak, Ben_US
dc.contributor.authorTyson, JJen_US
dc.date.accessioned2015-06-04T10:38:32Z
dc.date.issued1998-05en_US
dc.identifier.issn0301-4622en_US
dc.identifier.urihttp://qmro.qmul.ac.uk/xmlui/handle/123456789/7589
dc.description.abstractAlternating phases of DNA synthesis and mitosis, during the first 12 cell divisions of frog embryos, are driven by autonomous cytoplasmic oscillations of M-phase promoting factor (MPF). Cell-free extracts of frog eggs provide a convenient preparation for studying the molecular machinery that generates MPF oscillations and the surveillance mechanism that normally prevents entry into mitosis until chromosomal DNA is fully replicated. Early experiments suggested that unreplicated DNA blocks MPF activity by inducing phosphorylation of a crucial tyrosine residue, but recent evidence implicates a stoichiometric inhibitor (an MPF binding protein) as the `braking' agent. Using a realistic mathematical model of the mitotic control system in frog egg extracts, we suggest that both tyrosine phosphorylation and a stoichiometric inhibitors are involved in the block of MPF by unreplicated DNA. Both pathways operate by raising the cyclin threshold for MPF activation. As a bonus, in the process of analyzing these experiments, we obtain more direct and reliable estimates of the rate constants in the model.en_US
dc.format.extent169 - 184en_US
dc.relation.ispartofBiophysical Chemistryen_US
dc.titleModeling M-phase control in Xenopus oocyte extracts: the surveillance mechanism for unreplicated DNAen_US
dc.typeArticle
dc.identifier.doi10.1016/S0301-4622%2898%2900132-Xen_US
pubs.issue1-2en_US
pubs.notesNo embargoen_US
pubs.publication-statusPublisheden_US
pubs.volume72en_US


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