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Papers In Press, published online ahead of print September 10, 2001
J. Biol. Chem, 10.1074/jbc.M105152200
Submitted on June 5, 2001
Revised on August 22, 2001
Accepted on September 9, 2001
Cancer Research Labs, Queen's University, Kingston, Ontario K7L 3N6
Corresponding Author: sd13{at}post.queensu.ca
Cell cycle checkpoints are regulatory mechanisms that maintain genomic integrity by preventing cell cycle progression when genetic anomalies are present. The hRad9 protein is the human homologue of Schizosaccharomyces pombe Rad9, a checkpoint protein required for preventing the onset of mitosis if DNA damage is present or if DNA replication is incomplete. Genetic and biochemical analyses indicate that hRad9 is a component of the checkpoint response in humans, and has possible roles in regulating the cell cycle, apoptosis, and DNA repair. Previous studies have indicated that hRad9 is modified by phosphorylation, both in the absence of exogenous stress and in response to various genotoxins. In this study, we report the mapping of several sites of constitutive phosphorylation of hRad9 to [S/T]-P-X-[R/P] sequences near the C-terminus of the protein. We also demonstrate that a serine to alanine mutation at residue 272 abrogates an ionizing radiation (IR) induced phosphorylation of hRad9, and further show that phosphorylation at [S/T]-P sites is not a prerequisite for IR induced phosphorylation of serine 272. Finally, we report that hRad9 undergoes cell cycle regulated hyper-phosphorylation in G2/M that is enhanced by IR, but distinct from that on serine 272. Unlike the IR-induced phosphorylation at serine 272, this event is dependent on serine 277 and threonine 292, two C-terminal [S/T]-P sites in hRad9.
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