Stable overexpression of human HSF-1 in murine cells suggests activation rather than expression of HSF-1 to be the key regulatory step in the heat shock gene expression.

Abstract

Transcription of the heat shock genes is regulated by the activation of the heat shock transcription factor (HSF-1). After heat shock, HSF-1 forms oligomers and binds to the heat shock element (HSE), which consists of several repeats of NGAAN located in the promoter region of the heat shock genes. HSF-1 is then phosphorylated, leading to the enhanced transcription of the heat shock genes likely by transactivation. We have stably overexpressed the human heat shock transcription factor-1 (HSF-1) in murine cells to investigate whether the regulation of the expression of the heat shock genes may partly reside at the level of HSF-1 expression. Human HSF-1 cDNA was cloned into a retroviral vector (pvhhsf-1) and was overexpressed in a murine fibroblast cell line. The overexpressed human HSF-1 is found in both the cytoplasm and nucleus of control cells but is translocated into the nucleus upon heat shock. Electrophoretic mobility shift analysis suggests that the human HSF-1 has constitutive DNA binding ability and its DNA binding ability is increased upon heat shock. Cross-linking experiments indicate that the overexpressed human HSF-1 is mainly a monomer under control conditions and forms oligomers upon heat shock. Immunoblotting shows that the human HSF-1 is phosphorylated upon heat shock and its apparent molecular weight is shifted up by at least 10 kDa. In spite of both the DNA binding ability and phosphorylation, the overexpression of human HSF-1 does not increase the transcription of murine HSP-70 mRNA or increase the synthesis of other HSPs after heat shock beyond that observed in control untransfected cells. An exception is the enhanced synthesis of a 47-50 kDa protein after heat shock and an apparent lack of induction of one HSP-70 kDa species when the protein pattern is analyzed by isoelectric focusing. Interestingly, cells overexpressing human HSF-1 show a 4-fold increase in the basal expression of luciferase when the plasmids containing the human HSP-70 promoter ligated to the luciferase reporter gene are transiently expressed in these cells. Murine cells overexpressing human HSF-1 are more resistant to the cytotoxic effects of heat when compared to the control untransfected cells, but the kinetics of thermotolerance development and decay is similar between HSF-1 transfected and untransfected cells. In conclusion, human HSF-1 protein in murine fibroblasts is modified in a similar fashion as the endogenous mouse HSF-1 after heat shock. However, the overexpression of HSF-1 does not result in overproduction of heat shock proteins after heat shock, perhaps because these cells contain abundant amounts of endogenous HSF-1.