Victor M, Benecke B J
Department of Biochemistry, Ruhr-University Bochum, Germany.
Mol Biol Rep. 1998 Jul;25(3):135-41. doi: 10.1023/a:1006801205904.
The expression patterns of two mammalian heat shock factors (HSFs) were analysed in cell systems known to reflect an altered heat shock response. For being able to discriminate between the two closely related factors HSF 1 and HSF 2, specific cDNA sequences were cloned and used to generate antisense RNAs as hybridization probes. In general, in various cell lines expression of the two heat shock factors was clearly different. These expression patterns of the HSF genes were not influenced by retinoic acid-induced differentiation of human NT2 and mouse F9 teratocarcinoma cells. Generally, HSF 2 expression was extremely low, whereas the significantly higher expression of HSF 1 revealed cell specific differences. The highest expression rates of both HSFs were observed in 293 cells. To examine whether these high levels are involved in the constitutive expression of heat shock genes in these cells, we analysed the binding pattern of 293 cell proteins to the heat shock elements (HSEs). As with other cells, HSE-binding activity in 293 cells was only observed after heat shock treatment. This points to an HSE-independent way for high level expression of heat shock genes in these cells.
在已知能反映热休克反应改变的细胞系统中分析了两种哺乳动物热休克因子(HSF)的表达模式。为了能够区分两个密切相关的因子HSF 1和HSF 2,克隆了特定的cDNA序列并用于生成反义RNA作为杂交探针。一般来说,在各种细胞系中,两种热休克因子的表达明显不同。HSF基因的这些表达模式不受视黄酸诱导的人NT2和小鼠F9畸胎瘤细胞分化的影响。通常,HSF 2的表达极低,而HSF 1的明显较高表达显示出细胞特异性差异。在293细胞中观察到两种HSF的最高表达率。为了检查这些高水平是否参与这些细胞中热休克基因的组成型表达,我们分析了293细胞蛋白与热休克元件(HSE)的结合模式。与其他细胞一样,293细胞中的HSE结合活性仅在热休克处理后才观察到。这表明这些细胞中热休克基因高水平表达存在一种不依赖HSE的方式。