Mik1 levels accumulate in S phase and may mediate an intrinsic link between S phase and mitosis
- *Medical Research Council Cell Mutation Unit, Sussex University, Falmer, Sussex, BN1 9RR, United Kingdom; and †Department of Genetics, Institute of Molecular Biology, University of Copenhagen, Copenhagen DK 1353, Denmark
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Edited by Paul Nurse, Imperial Cancer Research Fund, London, United Kingdom, and approved January 7, 2000 (received for review September 20, 1999)
Abstract
Two paradigms exist for maintaining order during cell-cycle progression: intrinsic controls, where passage through one part of the cell cycle directly affects the ability to execute another, and checkpoint controls, where external pathways impose order in response to aberrant structures. By studying the mitotic inhibitor Mik1, we have identified evidence for an intrinsic link between unperturbed S phase and mitosis. We propose a model in which S/M linkage can be generated by the production and stabilization of Mik1 protein during S phase. The production of Mik1 during unperturbed S phase is independent of the Rad3- and Cds1-dependent checkpoint controls. In response to perturbed S phase, Rad3-Cds1 checkpoint controls are required to maintain high levels of Mik1, probably indirectly by extending the S phase period, where Mik1 is stable. In addition, we find that Mik1 protein can be moderately induced in response to irradiation of G2 cells in a Chk1-dependent manner.
Footnotes
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↵ ‡ To whom reprint requests should be addressed. E-mail: a.m.carr{at}sussex.ac.uk.
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This paper was submitted directly (Track II) to the PNAS office.
- Abbreviations:
- HU,
- hydroxyurea;
- FACS,
- fluorescence-activated cell sorter;
- DAPI,
- 4′,6-diamidino-2-phenylindole
- Copyright © 2000, The National Academy of Sciences








