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The heat shock response in HeLa cells is accompanied by elevated expression of the c-fos proto-oncogene.

机译:HeLa细胞中的热休克反应伴随着c-fos原癌基因的表达升高。

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摘要

Several known inducers of the heat shock response (heat stress, arsenite, and heavy metals) were shown to cause a significant elevation of c-fos mRNA in HeLa cells. Heat stress resulted in a time- and temperature-dependent prolonged elevation in the level of c-fos mRNA, which was accompanied by increased translation of c-fos protein and its appearance in the nucleus. Elevated expression of c-fos during heat stress was paralleled by induction of hsp 70 mRNA, while levels of c-myc and metallothionein mRNAs declined. Treatment of HeLa cells with arsenite or heavy metals also resulted in increased levels of hsp 70, as well as c-fos mRNA. Although elevated expression of c-fos was prevented by inhibitors of RNA synthesis, analysis of relative rates of gene transcription showed that during heat stress there was a negligible change in c-fos transcription. Therefore, the enhanced expression of c-fos during the heat shock response is likely to occur primarily through posttranscriptional processes. Cycloheximide was also shown to significantly increase the c-fos mRNA level in HeLa cells. There results are consistent with the observation that these inducers of the heat shock response, as well as cycloheximide, repress protein synthesis and suggest that the increase in the level of c-fos mRNA is caused by an inhibition of protein synthesis. This supports the hypothesis that c-fos mRNA is preferentially stabilized under conditions which induce the heat shock response, perhaps by decreased synthesis of a short-lived protein which regulates c-fos mRNA turnover.
机译:几种已知的热休克反应诱导物(热应激,亚砷酸盐和重金属)已导致HeLa细胞中c-fos mRNA显着升高。热应激导致c-fos mRNA的水平随时间和温度的延长升高,并伴有c-fos蛋白的翻译增加及其在细胞核中的出现。热应激期间c-fos的表达增加与hsp 70 mRNA的诱导平行,而c-myc和金属硫蛋白mRNA的水平下降。用亚砷酸盐或重金属处理HeLa细胞也导致hsp 70以及c-fos mRNA水平升高。尽管通过RNA合成抑制剂可以阻止c-fos的高表达,但是对基因转录相对速率的分析显示,在热应激期间,c-fos转录的变化可忽略不计。因此,在热激反应过程中c-fos的表达增强很可能主要通过转录后过程发生。还显示出环己酰亚胺可显着增加HeLa细胞中c-fos mRNA的水平。这些结果与以下观察结果一致,即这些热休克反应的诱导物以及环己酰亚胺抑制蛋白质合成,并暗示c-fos mRNA水平的增加是由蛋白质合成的抑制引起的。这支持了以下假设:c-fos mRNA在诱导热休克反应的条件下优先稳定,这可能是由于调节c-fos mRNA转换的短寿蛋白的合成减少。

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