Kumagai A, Dunphy W G
Division of Biology, Howard Hughes Medical Institute, California Institute of Technology, Pasadena 91125, USA.
Mol Cell. 2000 Oct;6(4):839-49. doi: 10.1016/s1097-2765(05)00092-4.
We have identified Claspin, a novel protein that binds to Xenopus Chk1 (Xchk1). Binding of Claspin to Xchk1 is highly elevated in the presence of DNA templates that trigger a checkpoint arrest of the cell cycle in Xenopus egg extracts. Xchk1 becomes phosphorylated during a checkpoint response, and we demonstrate directly that this phosphorylation results in the activation of Xchk1. Immunodepletion of Claspin from egg extracts abolishes both the phosphorylation and activation of Xchk1. Furthermore, Claspin-depleted extracts are unable to arrest the cell cycle in response to DNA replication blocks. Taken together, these findings indicate that Claspin is an essential upstream regulator of Xchk1.
我们鉴定出了Claspin,一种与非洲爪蟾Chk1(Xchk1)结合的新型蛋白质。在能触发非洲爪蟾卵提取物中细胞周期关卡停滞的DNA模板存在时,Claspin与Xchk1的结合显著增强。Xchk1在关卡反应过程中发生磷酸化,并且我们直接证明这种磷酸化导致Xchk1的激活。从卵提取物中免疫去除Claspin会消除Xchk1的磷酸化和激活。此外,去除Claspin的提取物无法响应DNA复制阻滞而使细胞周期停滞。综上所述,这些发现表明Claspin是Xchk1必不可少的上游调节因子。