Cdc6 is regulated by E2F and is essential for DNA replication in mammalian cells
- Zhen Yan*,
- James DeGregori†,
- Ralph Shohet*,
- Gustavo Leone†,
- Bruce Stillman‡,
- Joseph R. Nevins†, and
- R. Sanders Williams*,§
- *University of Texas Southwestern Medical Center, Dallas, TX 75235; †Duke University Medical Center, Durham, NC 27710; and ‡Cold Spring Harbor Laboratory, Cold Spring Harbor, NY 11724
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Communicated by Steven L. McKnight, University of Texas Southwestern, Dallas, TX (received for review October 21, 1997)
Abstract
Cdc6 has a critical regulatory role in the initiation of DNA replication in yeasts, but its function in mammalian cells has not been characterized. We show here that Cdc6 is expressed selectively in proliferating but not quiescent mammalian cells, both in culture and within tissues of intact animals. During the transition from a growth-arrested to a proliferative state, transcription of mammalian Cdc6 is regulated by E2F proteins, as revealed by a functional analysis of the human Cdc6 promoter and by the ability of exogenously expressed E2F proteins to stimulate the endogenous Cdc6 gene. Immunodepletion of Cdc6 by microinjection of anti-Cdc6 antibody blocks initiation of DNA replication in a human tumor cell line. We conclude that expression of human Cdc6 is regulated in response to mitogenic signals though transcriptional control mechanisms involving E2F proteins, and that Cdc6 is required for initiation of DNA replication in mammalian cells.
Footnotes
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↵ § University of Texas Southwestern Medical Center, 5323 Harry Hines Boulevard, NB11.200, Dallas, TX 75235-8573. e-mail: williams{at}ryburn.swmed.edu.
- ABBREVIATION:
- ORC,
- origin recognition complex
- Copyright © 1998, The National Academy of Sciences





