Shim J, Lee H, Park J, Kim H, Choi E J
The Cell Biology Laboratory, Hanhyo Institutes of Technology, Kyongki-do, Korea.
Nature. 1996 Jun 27;381(6585):804-6. doi: 10.1038/381804a0.
The stress-activated protein kinases (SAPKs), which are identical to the c-Jun amino-terminal kinases (JNKs), are activated in response to a variety of cellular stresses, including DNA damage, heat shock or tumour-necrosis factor-alpha. SAPK, a subfamily of the mitogen-activated protein (MAP) kinases, is a major protein kinase that phosphorylates c-Jun and other transcription factors. SAPK phosphorylation of transcription factors is important in stress-activated signalling cascades. Here we report that the protein p21 WAF1/CIP1/Sd:1, a DNA-damage-inducible cell-cycle inhibitor, acts as an inhibitor of the SAPK group of mammalian MAP kinases. This highlights a new biochemical activity of p21, which may provide the first evidence for a non-enzymatic inhibitory protein for SAPK. We suggest that p21, by inhibiting SAPK, may participate in regulating signalling cascades that are activated by cellular stresses such as DNA damage.
应激激活蛋白激酶(SAPK)与c-Jun氨基末端激酶(JNK)相同,可响应多种细胞应激而被激活,包括DNA损伤、热休克或肿瘤坏死因子-α。SAPK是丝裂原激活蛋白(MAP)激酶的一个亚家族,是一种主要的蛋白激酶,可使c-Jun和其他转录因子磷酸化。转录因子的SAPK磷酸化在应激激活的信号级联反应中很重要。我们在此报告,蛋白p21 WAF1/CIP1/Sd:1是一种DNA损伤诱导的细胞周期抑制剂,可作为哺乳动物MAP激酶SAPK组的抑制剂。这突出了p21的一种新的生化活性,这可能为SAPK的非酶抑制蛋白提供首个证据。我们认为,p21通过抑制SAPK,可能参与调节由DNA损伤等细胞应激激活的信号级联反应。