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PMID: 9288745 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Loading of an Mcm protein onto DNA replication origins is regulated by Cdc6p and CDKs.

Cell ·Vol. 90 ·No. 4 ·1997-08-22 ·Pages 649-60

Tanaka T, Knapp D, Nasmyth K

Abstract

In eukaryotic cells, firing of DNA replication origins normally does not recur until after M phase. This characteristic is thought to be due to the properties of "initiation" proteins like Orc, Cdc6, and Mcms. Using formaldehyde cross-linking, we show that Cdc6p and Mcm7p associate specifically with replication origins during G1 but not during G2 in S. cerevisiae. Mcm7p's association with origins depends on Cdc6p. Ectopic expression of Cdc6p enables it to associate with origins during G2, but this fails to recruit Mcm7p. Our data suggest that the loading of Mcm proteins onto origins is regulated by two mechanisms: first, by Cdc6p occupancy, and second, by S- and M-CDKs, whose activity during S, G2, and M phases prevents Mcm loading.

MeSH Terms
Binding Sites Cell Cycle Proteins/metabolism Cyclin-Dependent Kinases/metabolism DNA Replication DNA-Binding Proteins/metabolism Fungal Proteins/metabolism G1 Phase G2 Phase Minichromosome Maintenance Complex Component 7 Mitosis Nuclear Proteins/metabolism Origin Recognition Complex Protein Binding Saccharomyces cerevisiae Saccharomyces cerevisiae Proteins
Chemicals
CDC6 protein, S cerevisiae Cell Cycle Proteins DNA-Binding Proteins Dbf4 protein, S cerevisiae Fungal Proteins MCM5 protein, S cerevisiae MCM5 protein, human Nuclear Proteins Origin Recognition Complex Saccharomyces cerevisiae Proteins Cyclin-Dependent Kinases MCM7 protein, S cerevisiae Minichromosome Maintenance Complex Component 7
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Tanaka T
Research Institute of Molecular Pathology, Vienna, Austria.
Knapp D
Nasmyth K
Article Info
Journal
Cell
Abbr.
Cell
ISSN
0092-8674
Published
1997-08-22
Pages
649-60
Language
English
Region
United States
NLM ID
0413066
Subset
IM
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