Takenaka K, Moriguchi T, Nishida E
Department of Biophysics, Graduate School of Science, Kyoto University, Kitashirakawa-Oiwake, Sakyo-ku, Kyoto 606-01, Japan.
Science. 1998 Apr 24;280(5363):599-602. doi: 10.1126/science.280.5363.599.
The mitogen-activated protein kinase (MAPK) superfamily comprises classical MAPK (also called ERK), c-Jun amino-terminal or stress-activated protein kinase (JNK or SAPK), and p38. Although MAPK is essential for meiotic processes in Xenopus oocytes and the spindle assembly checkpoint in Xenopus egg extracts, the role of members of the MAPK superfamily in M phase or the spindle assembly checkpoint during somatic cell cycles has not been elucidated. The kinase p38, but not MAPK or JNK, was activated in mammalian cultured cells when the cells were arrested in M phase by disruption of the spindle with nocodazole. Addition of activated recombinant p38 to Xenopus cell-free extracts caused arrest of the extracts in M phase, and injection of activated p38 into cleaving embryos induced mitotic arrest. Treatment of NIH 3T3 cells with a specific inhibitor of p38 suppressed activation of the checkpoint by nocodazole. Thus, p38 functions as a component of the spindle assembly checkpoint in somatic cell cycles.
丝裂原活化蛋白激酶(MAPK)超家族包括经典的MAPK(也称为ERK)、c-Jun氨基末端激酶或应激激活蛋白激酶(JNK或SAPK)以及p38。虽然MAPK对于非洲爪蟾卵母细胞的减数分裂过程以及非洲爪蟾卵提取物中的纺锤体组装检查点至关重要,但MAPK超家族成员在体细胞周期的M期或纺锤体组装检查点中的作用尚未阐明。当用诺考达唑破坏纺锤体使哺乳动物培养细胞停滞在M期时,激酶p38被激活,而MAPK或JNK未被激活。将活化的重组p38添加到非洲爪蟾无细胞提取物中会导致提取物停滞在M期,并且将活化的p38注射到正在分裂的胚胎中会诱导有丝分裂停滞。用p38的特异性抑制剂处理NIH 3T3细胞可抑制诺考达唑对检查点的激活。因此,p38在体细胞周期中作为纺锤体组装检查点的一个组成部分发挥作用。