Mankowitz L, Staffas L, Bakke M, Lund J
Department of Biochemistry, Wallenberg Laboratory, Stockholm University, Sweden.
Biochem J. 1995 Jan 1;305 ( Pt 1)(Pt 1):111-8. doi: 10.1042/bj3050111.
Three different forms of glutathione transferase (GST) have been resolved in the two mouse adrenal tumour cell lines Y1 and Kin 8. Two of these belong to the mu and pi classes respectively. The third form is so far unidentified. In the Y1 cells, the levels of the mu form (mGTmu1) and the unidentified form, are both down-regulated in the presence of adrenocorticotrophic hormone (ACTH) while the pi form is unaffected. The Kin 8 cell line is derived from Y1 cells and harbours a defect in the cyclic AMP (cAMP)-dependent protein kinase, making it refractory to cAMP-dependent regulation of several enzymes. The GST levels in this cell line were unaffected by ACTH. Also, the steady-state levels of mGTmu1 mRNA were much lower in Y1 cells treated with forskolin (which activates adenylate cyclase) compared with control cells, but there was no difference in mGTmu1 mRNA levels between control and forskolin-treated Kin 8 cells. This indicates that the ACTH-dependent regulation of the mu class GST is pre-translational and that a functional cAMP-dependent protein kinase is required for the regulation. We have further shown that the difference in mRNA steady-state levels between control and forskolin-treated Y1 cells is abolished when transcription is inhibited by actinomycin D. In light of the stability of mGTmu1 mRNA, it would appear most likely that actinomycin D inhibits the transcription of short-lived factors which regulate the turn-over of mGTmu1 transcripts in response to changes in intracellular cAMP levels.
在两种小鼠肾上腺肿瘤细胞系Y1和Kin 8中已分辨出三种不同形式的谷胱甘肽转移酶(GST)。其中两种分别属于μ类和π类。第三种形式迄今尚未明确。在Y1细胞中,μ形式(mGTmu1)和未明确形式的水平在促肾上腺皮质激素(ACTH)存在时均下调,而π形式不受影响。Kin 8细胞系源自Y1细胞,在环磷酸腺苷(cAMP)依赖性蛋白激酶中存在缺陷,使得它对几种酶的cAMP依赖性调节不敏感。该细胞系中的GST水平不受ACTH影响。此外,与对照细胞相比,用福斯可林(激活腺苷酸环化酶)处理的Y1细胞中mGTmu1 mRNA的稳态水平要低得多,但对照和用福斯可林处理的Kin 8细胞之间的mGTmu1 mRNA水平没有差异。这表明μ类GST的ACTH依赖性调节是在翻译前进行的,并且调节需要功能性的cAMP依赖性蛋白激酶。我们进一步表明,当用放线菌素D抑制转录时,对照和用福斯可林处理的Y1细胞之间mRNA稳态水平的差异消失。鉴于mGTmu1 mRNA的稳定性,似乎最有可能的是放线菌素D抑制了短寿命因子的转录,这些因子响应细胞内cAMP水平的变化调节mGTmu1转录本的周转。