Control of the Cdc2/cyclin B complex in Xenopus egg extracts arrested at a G2/M checkpoint with DNA synthesis inhibitors
- Creators
-
Kumagai, Akiko
-
Dunphy, William G.
Abstract
Proliferating eukaryotic cells possess checkpoint mechanisms that block cell division in the presence of unreplicated or damaged DNA. Using cell-free extracts from Xenopus eggs, we have investigated the mechanisms underlying the inability of a recombinant Cdc2/cyclin B complex to induce mitosis in the presence of incompletely replicated DNA. We found that the activities of the kinases and phosphatases that regulate the major phosphorylation sites on Cdc2 (e.g., tyrosine 15, threonine 14, and threonine 161) are not altered significantly under conditions where Xenopus extracts remain stably arrested in interphase due to the presence of the replication inhibitor aphidicolin. However, at threshold concentrations, a Cdc2/cyclin B complex containing a mutant Cdc2 subunit that cannot be phosphorylated on either tyrosine 15 or threonine 14 displays a markedly reduced capacity to induce mitosis in the presence of aphidicolin. This observation indicates that the replication checkpoint in Xenopus egg extracts functions without the inhibitory tyrosine and threonine phosphorylation of Cdc2. We provide evidence that the checkpoint-dependent suppression of the Cdc2/cyclin B complex involves a titratable inhibitor that is regulated by the presence of unreplicated DNA.
Additional Information
Copyright © 1995 by The American Society for Cell Biology. Under the License and Publishing Agreement, authors grant to the general public, effective two months after publication of (i.e.,. the appearance of) the edited manuscript in an online issue of MBoC, the nonexclusive right to copy, distribute, or display the manuscript subject to the terms of the Creative Commons–Noncommercial–Share Alike 3.0 Unported license (http://creativecommons.org/licenses/by-nc-sa/3.0). Submitted November 18, 1994; Accepted January 11, 1995. Monitoring Editor: Tim Hunt We thank our colleagues for comments on the manuscript. We are grateful to D. Morgan (University of California, San Francisco) for providing a baculovirus vector for histidine tagging. M. Solomon (Yale University) kindly provided the Cdc2 mutant plasmids. This work was supported by grants from the National Institutes of Health, Lucille P. Markey Charitable Trust, National Science Foundation, and Gustavus and Louise Pfeiffer Foundation. W.G.D. is an investigator of the Howard Hughes Medical Institute.Attached Files
Published - KUMmbc95.pdf
Files
| Name | Size | Download all |
|---|---|---|
|
md5:e40d98bb7cab171e123c9fa34482319f
|
3.8 MB | Preview Download |
Additional details
- PMCID
- PMC275829
- Eprint ID
- 3895
- Resolver ID
- CaltechAUTHORS:KUMmbc95
- NIH
- Lucille P. Markey Charitable Trust
- Gustavus and Louise Pfeiffer Foundation
- Howard Hughes Medical Institute (HHMI)
- Created
-
2006-07-18Created from EPrint's datestamp field
- Updated
-
2020-03-09Created from EPrint's last_modified field