Karlsson-Rosenthal Christina, Millar Jonathan B A
Department of Cell and Molecular Biology, Karolinska Institute, S-171 77 Stockholm, Sweden.
Trends Cell Biol. 2006 Jun;16(6):285-92. doi: 10.1016/j.tcb.2006.04.002. Epub 2006 May 8.
Members of the eukaryotic Cdc25 phosphatase family are key targets of the Chk1 and Chk2 checkpoint kinases, which inactivate Cdc25 to halt cell cycle progression when DNA is damaged or incompletely replicated. Now, new kinases that phosphorylate and inactivate Cdc25 are being discovered, including MAPKAP kinase-2, a component of the p38 stress-activated MAP kinase pathway. The roles of other kinases, such as cyclin-dependent kinase, Polo and Aurora A kinase, in controlling the localization or the activation of Cdc25, are controversial. Here, we discuss new data that suggests that different Cdc25 isoforms and regulators of Cdc25 are differentially required for normal cell cycle progression and recovery from checkpoint arrest.
真核生物Cdc25磷酸酶家族成员是Chk1和Chk2检查点激酶的关键靶点,当DNA受损或复制不完全时,Chk1和Chk2会使Cdc25失活,从而阻止细胞周期进程。现在,人们发现了新的能使Cdc25磷酸化并使其失活的激酶,包括p38应激激活的丝裂原活化蛋白激酶(MAPK)途径的组成部分MAPKAP激酶-2。其他激酶,如细胞周期蛋白依赖性激酶、Polo激酶和Aurora A激酶,在控制Cdc25的定位或激活方面所起的作用存在争议。在这里,我们讨论的新数据表明,正常细胞周期进程以及从检查点阻滞中恢复需要不同的Cdc25亚型和Cdc25调节剂。