Ghoshal K, Jacob S T
Department of Pharmacology and Molecular Biology, Chicago Medical School, North Chicago, IL 60064, USA.
Biochem J. 1996 Aug 1;317 ( Pt 3)(Pt 3):689-95. doi: 10.1042/bj3170689.
The effect of heat shock on RNA polymerase I (pol I)-directed transcription of the rRNA gene was studied in S-100 extract derived from mouse lymphosarcoma cells, and by in vivo labelling of rRNA. Exposure of cells to 42 degrees C for 2 h resulted in complete inhibition of rRNA synthesis in vivo. Pol I transcription was inhibited by 50% within 2 h of heat shock and was abolished after 3 h exposure at 42 degrees C. Under this condition, the core-promoter-binding activity of the factor (CPBF) that modulates pol I transcription was unaffected. In contrast, the promoter-binding activity of enhancer-1-binding factor, a protein related to the Ku autoantigen, which is involved in pol I transcription initiation, was reduced by 50 and 90% after 2 and 3 h of heat shock respectively. Western-blot analysis with antibodies specific for the two subunits of Ku protein showed the absence of p72 subunit after 3 h of heat shock. Under this condition, pol II transcription from the adenovirus major late promoter and pol III transcription of 5 S RNA gene remained unaffected. Mixing experiments ruled out the possibility that the inhibition of transcription was due to activation of nucleases or other inhibitors. This is the first report to show selective down-regulation of pol I transcription in vitro by heat shock and of the potential involvement of a pol I transcription factor in this process.
在源自小鼠淋巴肉瘤细胞的S-100提取物中,以及通过对rRNA进行体内标记,研究了热休克对RNA聚合酶I(pol I)指导的rRNA基因转录的影响。将细胞暴露于42℃ 2小时导致体内rRNA合成完全抑制。热休克2小时内,pol I转录被抑制50%,在42℃暴露3小时后被完全抑制。在此条件下,调节pol I转录的因子(CPBF)的核心启动子结合活性未受影响。相反,增强子-1结合因子的启动子结合活性,一种与Ku自身抗原相关的蛋白质,其参与pol I转录起始,在热休克2小时和3小时后分别降低了50%和90%。用针对Ku蛋白两个亚基的特异性抗体进行的蛋白质印迹分析表明,热休克3小时后p72亚基缺失。在此条件下,腺病毒主要晚期启动子的pol II转录和5 S RNA基因的pol III转录未受影响。混合实验排除了转录抑制是由于核酸酶或其他抑制剂激活的可能性。这是第一份显示热休克在体外选择性下调pol I转录以及pol I转录因子可能参与这一过程的报告。