Israel D I, Estolano M G, Galeazzi D R, Whitlock J P
J Biol Chem. 1985 May 10;260(9):5648-53.
Inhibition of protein synthesis superinduces transcription of the cytochrome P1-450 gene in Hepa 1c1c7 mouse hepatoma cells. The superinduced transcription rate is 10-15-fold higher than the maximal rate of transcription induced by the known inducer 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) alone. Superinduction is maximal within 30-40 min and remains maximal for at least 90 min. Cytochrome P1-450 mRNA is the same length in TCDD-induced and superinduced cells. Superinduction does not occur in variant cells in which TCDD-receptor complexes bind weakly to nuclei and which do not transcribe the cytochrome P1-450 gene in response to TCDD. Inhibition of protein synthesis does not alter several properties of TCDD-receptor complexes. The results imply that a second control mechanism modulates the action of the TCDD-receptor complex in regulating cytochrome P1-450 gene transcription.
蛋白质合成的抑制超诱导了Hepa 1c1c7小鼠肝癌细胞中细胞色素P1 - 450基因的转录。超诱导的转录速率比已知诱导剂2,3,7,8 - 四氯二苯并 - p - 二恶英(TCDD)单独诱导的最大转录速率高10 - 15倍。超诱导在30 - 40分钟内达到最大值,并至少持续90分钟保持最大值。细胞色素P1 - 450 mRNA在TCDD诱导的细胞和超诱导的细胞中长度相同。在TCDD受体复合物与细胞核弱结合且不响应TCDD转录细胞色素P1 - 450基因的变异细胞中不发生超诱导。蛋白质合成的抑制不会改变TCDD受体复合物的几个特性。结果表明,第二种控制机制调节TCDD受体复合物在调节细胞色素P1 - 450基因转录中的作用。