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通过抑制野生型和变异型小鼠肝癌细胞中的蛋白质合成来超诱导细胞色素P1 - 450基因转录。

Superinduction of cytochrome P1-450 gene transcription by inhibition of protein synthesis in wild type and variant mouse hepatoma cells.

作者信息

Israel D I, Estolano M G, Galeazzi D R, Whitlock J P

出版信息

J Biol Chem. 1985 May 10;260(9):5648-53.

PMID:2985607
Abstract

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.

摘要

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。

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