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DNA replication checkpoint control of Wee1 stability by vertebrate Hsl7
Correspondence to Sally Kornbluth: Kornb001{at}mc.duke.edu
G2/M checkpoints prevent mitotic entry upon DNA damage or replication inhibition by targeting the Cdc2 regulators Cdc25 and Wee1. Although Wee1 protein stability is regulated by DNA-responsive checkpoints, the vertebrate pathways controlling Wee1 degradation have not been elucidated. In budding yeast, stability of the Wee1 homologue, Swe1, is controlled by a regulatory module consisting of the proteins Hsl1 and Hsl7 (histone synthetic lethal 1 and 7), which are targeted by the morphogenesis checkpoint to prevent Swe1 degradation when budding is inhibited. We report here the identification of Xenopus Hsl7 as a positive regulator of mitosis that is controlled, instead, by an entirely distinct checkpoint, the DNA replication checkpoint. Although inhibiting Hsl7 delayed mitosis, Hsl7 overexpression overrode the replication checkpoint, accelerating Wee1 destruction. Replication checkpoint activation disrupted Hsl7–Wee1 interactions, but binding was restored by active polo-like kinase. These data establish Hsl7 as a component of the replication checkpoint and reveal that similar cell cycle control modules can be co-opted for use by distinct checkpoints in different organsims.
Abbreviations used in this paper: ß-TrCP, ß transducin repeat containing protein; ELB, egg lysis buffer; GVBD, germinal vesicle breakdown; Hsl7, histone synthetic lethal 7; JBP1, Janus kinase binding protein 1; Plk1, Polo-like kinase; Plx1, Xenopus Polo-like kinase; SCF, Skp1–cullin–F box.
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