Human heat shock factor 1 is predominantly a nuclear protein before and after heat stress

Citation
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
Citations number
52
Categorie Soggetti
Cell & Developmental Biology
Journal title
JOURNAL OF CELL SCIENCE
ISSN journal
00219533 → ACNP
Volume
112
Issue
16
Year of publication
1999
Pages
2765 - 2774
Database
ISI
SICI code
0021-9533(199908)112:16<2765:HHSF1I>2.0.ZU;2-5
Abstract
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.