Chen C, Xie Y, Stevenson M A, Auron P E, Calderwood S K
Dana-Farber Cancer Institute and Joint Center for Radiation Therapy, Harvard Medical School, Boston, Massachusetts 02115, USA.
J Biol Chem. 1997 Oct 24;272(43):26803-6. doi: 10.1074/jbc.272.43.26803.
Heat shock factor 1, the critical molecular regulator of the stress response is conserved throughout eukaryotic organisms and activates the transcription of heat shock genes. We now show that heat shock factor 1 inhibits the expression of c-fos, an immediate early gene that controls responses to extracellular stimuli for growth and differentiation. Heat shock factor 1 inhibits the transcription of the c-fos gene and antagonizes the activating effects of the signal transducing protein Ras on the c-fos promoter and on the promoter of another Ras responsive gene uPA. This property was specific for heat shock factor 1; c-fos repression was not seen with the structurally related protein heat shock factor 2. Repression involved different molecular mechanisms compared with those involved in transcriptional activation by heat shock factor 1 and specifically did not require binding to the c-fos promoter. Thus, in addition to its known role as a transcriptional activator of the cellular heat shock response, heat shock factor 1 also antagonizes the expression of Fos, a key component of the ubiquitous AP-1 transcription factor complex and as such could influence multiple aspects of cell regulation.
热休克因子1是应激反应的关键分子调节因子,在整个真核生物中保守,并激活热休克基因的转录。我们现在表明,热休克因子1抑制c-fos的表达,c-fos是一种即时早期基因,控制对细胞外刺激的生长和分化反应。热休克因子1抑制c-fos基因的转录,并拮抗信号转导蛋白Ras对c-fos启动子和另一个Ras反应基因uPA启动子的激活作用。这种特性对热休克因子1具有特异性;与结构相关的蛋白热休克因子2相比,未观察到c-fos的抑制作用。与热休克因子1的转录激活相比,抑制涉及不同的分子机制,并且特别不需要与c-fos启动子结合。因此,除了其作为细胞热休克反应的转录激活剂的已知作用外,热休克因子1还拮抗Fos的表达,Fos是普遍存在的AP-1转录因子复合物的关键成分,因此可能影响细胞调节的多个方面。