S-phase checkpoint controls mitosis via an APC-independent Cdc20p function

Duncan J. Clarke, Marisa Segal, Catherine A. Andrews, Stanislav G. Rudyak, Sanne Jensen, Karen Smith, Steven I. Reed

Research output: Contribution to journalArticlepeer-review

34 Scopus citations


Cells divide with remarkable fidelity, allowing complex organisms to develop and possess longevity. Checkpoint controls contribute by ensuring that genome duplication and segregation occur without error so that genomic instability, associated with developmental abnormalities and a hallmark of most human cancers, is avoided. S-phase checkpoints prevent cell division while DNA is replicating. Budding yeast Mec1p and Rad53p, homologues of human checkpoint kinases ATM/ATR and Chk2, are needed for this control system. How Mec1p and Rad53p prevent mitosis in S phase is not known. Here we provide evidence that budding yeasts avoid mitosis during S phase by regulating the anaphase-promoting complex (APC) specificity factor Cdc20p: Mec1p and Rad53p repress the accumulation of Cdc20p in S phase. Because precocious Cdc20p accumulation causes anaphase onset and aneuploidy, Cdc20p concentrations must be precisely regulated during each and every cell cycle. Catastrophic mitosis induced by Cdc20p in S phase occurs even in the absence of core APC components. Thus, Cdc20p can function independently of the APC.

Original languageEnglish (US)
Pages (from-to)928-935
Number of pages8
JournalNature Cell Biology
Issue number10
StatePublished - Oct 1 2003

Bibliographical note

Funding Information:
We are grateful to Steve Haase, Lehland Johnston, Jim Hwang and Peter Kaiser for providing strains and plasmids. DJC was supported by US Army DOD Breast Cancer Research Grant BRCP-97-1-7059, SJ by the Danish Medical Research Council. This work was supported in part by NIH grant 1R01CA85487-02 (SIR), Basil O’Connor March of Dimes Starter Scholarship 5-FY02-248 (DJC) and NCI grant 1R01CA99033-01 (DJC).


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