A Caltech Library Service

Regulation of Saccharomyces cerevisiae CDC7 function during the cell cycle

Yoon, Hye-Joo and Loo, Seng and Campbell, Judith L. (1993) Regulation of Saccharomyces cerevisiae CDC7 function during the cell cycle. Molecular Biology of the Cell, 4 (2). pp. 195-208. ISSN 1059-1524. PMCID PMC300915.

PDF - Published Version
Creative Commons Attribution Non-commercial Share Alike.


Use this Persistent URL to link to this item:


The yeast Cdc7 function is required for the G1/S transition and is dependent on passage through START, a point controlled by the Cdc28/cdc2/p34 protein kinase. CDC7 encodes a protein kinase activity, and we now show that this kinase activity varies in the cell cycle but that protein levels appear to remain constant. We present several lines of evidence that periodic activation of CDC7 kinase is at least in part through phosphorylation. First, the kinase activity of the Cdc7 protein is destroyed by dephosphorylation of the protein in vitro with phosphatase. Second, Cdc7 protein is hypophosphorylated and inactive as a kinase in extracts of cells arrested at START but becomes active and maximally phosphorylated subsequent to passage through START. The phosphorylation pattern of Cdc7 protein is complex. Phosphopeptide mapping reveals four phosphopeptides in Cdc7 prepared from asynchronous yeast cells. Both autophosphorylation and phosphorylation in trans appear to contribute to this pattern. Autophosphorylation is shown to occur by using a thermolabile Cdc7 protein. A protein in yeast extracts can phosphorylate and activate Cdc7 protein made in Escherichia coli, and phosphorylation is thermolabile in cdc28 mutant extracts. Cdc7 protein carrying a serine to alanine change in the consensus recognition site for Cdc28 kinase shows an altered phosphopeptide map, suggesting that this site is important in determining the overall Cdc7 phosphorylation pattern.

Item Type:Article
Related URLs:
URLURL TypeDescription CentralArticle
Additional Information:Copyright © 1993 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 ( Submitted November 2, 1992; Accepted December 16, 1992 We are grateful to M. Tyers, B. Futcher, C. Wittenberg, and W. Dunphy who provided the Cdc28 reagents for this study and to William Dunphy for discussion and comments on the manuscript. This work was supported by USPHS GM25508 and NSF CHE8509637.
Funding AgencyGrant Number
Issue or Number:2
PubMed Central ID:PMC300915
Record Number:CaltechAUTHORS:YOOmbc93
Persistent URL:
Usage Policy:No commercial reproduction, distribution, display or performance rights in this work are provided.
ID Code:3897
Deposited By: Archive Administrator
Deposited On:18 Jul 2006
Last Modified:02 Oct 2019 23:07

Repository Staff Only: item control page