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PMID: 1310257 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Oscillation of MPF is accompanied by periodic association between cdc25 and cdc2-cyclin B.

Cell ·Vol. 68 ·No. 2 ·1992-01-24 ·Pages 323-32

Jessus C, Beach D

Abstract

Activation of maturation-promoting factor at the onset of mitosis requires the tyrosine dephosphorylation of one of its components, the cdc2 protein kinase. cdc25 is the specific tyrosine phosphatase that activates cdc2. We find that Xenopus oocytes contain a relative of cdc25, p72. In Xenopus embryos the abundance of p72 does not oscillate during the cell cycle. However, p72 directly associates with cdc2-cyclin B in a cell cycle-dependent manner, reaching a peak at M phase. The M phase kinase that associates with p72 is catalytically active. These results suggest that the mechanism by which cdc25 triggers cdc2 activation involves a periodic physical association between cdc25 and the cyclin B-cdc2 complex and also that mitotic control can be affected by mechanisms other than transcriptional regulation of the cdc25 gene.

MeSH Terms
Animals Blotting, Western CDC2 Protein Kinase/metabolism Cell Cycle Proteins Cross Reactions Cyclins/metabolism Fungal Proteins/metabolism Kinetics Macromolecular Substances Maturation-Promoting Factor/metabolism Oocytes/metabolism Protamine Kinase/metabolism Xenopus laevis ras-GRF1
Chemicals
Cell Cycle Proteins Cyclins Fungal Proteins Macromolecular Substances ras-GRF1 Protamine Kinase CDC2 Protein Kinase Maturation-Promoting Factor
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Jessus C
Howard Hughes Medical Institute, Cold Spring Harbor Laboratory, New York 11724.
Beach D
Article Info
Journal
Cell
Abbr.
Cell
ISSN
0092-8674
Published
1992-01-24
Pages
323-32
Language
English
Region
United States
NLM ID
0413066
Subset
IM
Grants
NIGMS NIH HHS · GM69620 · United States
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