Pa. Mercier et al., Human heat shock factor 1 is predominantly a nuclear protein before and after heat stress, J CELL SCI, 112(16), 1999, pp. 2765-2774
The induction of the heat shock genes in eukaryotes by heat and other forms
of stress is mediated by a transcription factor known as heat shock factor
1 (HSF1). HSF1 is present in unstressed metazoan cells as a monomer with l
ow affinity for DNA, and upon exposure to stress it is converted to an 'act
ive' homotrimer that binds the promoters of heat shock genes with high affi
nity and induces their transcription. The conversion of HSF1 to its active
form is hypothesized to be a multistep process involving physical changes i
n the HSF1 molecule and the possible translocation of HSF1 from the cytopla
sm to the nucleus. While all studies to date have found active HSF1 to be a
nuclear protein, there have been conflicting reports on whether the inacti
ve form of HSF is predominantly a cytoplasmic or nuclear protein. In this s
tudy, we have made antibodies against human HSF1 and have reexamined its lo
calization in unstressed and heat-shocked human HeLa and A549 cells, and in
green monkey Vero cells. Biochemical fractionation of heat-shocked HeLa ce
lls followed by western blot analysis showed that HSF1 was mostly found in
the nuclear fraction. In extracts made from unshocked cells, HSF1 was predo
minantly found in the cytoplasmic fraction using one fractionation procedur
e, but was distributed approximately equally between the cytoplasmic and nu
clear fractions when a different procedure was used. Immunofluorescence mic
roscopy revealed that HSF1 was predominantly a nuclear protein in both heat
shocked and unstressed cells. Quantification of HSF1 staining showed that
approximately 80% of HSF1 was present in the nucleus both before and after
heat stress. These results suggest that HSF1 is predominantly a nuclear pro
tein prior to being exposed to stress, but has low affinity for the nucleus
and is easily extracted using most biochemical fractionation procedures. T
hese results also imply that HSF1 translocation is probably not part of the
multistep process in HSF1 activation for many cell types.