Yujiri T, Sather S, Fanger G R, Johnson G L
Program in Molecular Signal Transduction, Division of Basic Sciences, National Jewish Medical and Research Center, Denver, CO 80206, USA.
Science. 1998 Dec 4;282(5395):1911-4. doi: 10.1126/science.282.5395.1911.
Targeted disruption of the gene encoding MEK kinase 1 (MEKK1), a mitogen-activated protein kinase (MAPK) kinase kinase, defined its function in the regulation of MAPK pathways and cell survival. MEKK1(-/-) embryonic stem cells from mice had lost or altered responses of the c-Jun amino-terminal kinase (JNK) to microtubule disruption and cold stress but activated JNK normally in response to heat shock, anisomycin, and ultraviolet irradiation. Activation of JNK was lost and that of extracellular signal-regulated protein kinase (ERK) was diminished in response to hyperosmolarity and serum factors in MEKK1(-/-) cells. Loss of MEKK1 expression resulted in a greater apoptotic response of cells to hyperosmolarity and microtubule disruption. When activated by specific stresses that alter cell shape and the cytoskeleton, MEKK1 signals to protect cells from apoptosis.
有丝分裂原激活蛋白激酶(MAPK)激酶激酶——MEK激酶1(MEKK1)编码基因的靶向破坏,确定了其在MAPK信号通路调节和细胞存活中的功能。来自小鼠的MEKK1(-/-)胚胎干细胞对微管破坏和冷应激失去或改变了c-Jun氨基末端激酶(JNK)的反应,但在热休克、茴香霉素和紫外线照射下能正常激活JNK。在MEKK1(-/-)细胞中,高渗和血清因子会导致JNK激活丧失,细胞外信号调节蛋白激酶(ERK)激活减弱。MEKK1表达缺失导致细胞对高渗和微管破坏的凋亡反应增强。当被改变细胞形状和细胞骨架的特定应激激活时,MEKK1发出信号保护细胞免于凋亡。