Heat shock factor

In molecular biology, heat shock factors (HSF), are the transcription factors that regulate the expression of the heat shock proteins.[1][2] A typical example is the heat shock factor of Drosophila melanogaster.[3]

HSF-type DNA-binding
Structure of the dimeric DNA binding domain of the yeast heat shock factor (cyan and green) bound to DNA (brown) based on PDB: 3HTS​.
Identifiers
SymbolHSF_DNA-bind
PfamPF00447
InterProIPR000232
PROSITEPDOC00381
SCOP21hks / SCOPe / SUPFAM
Available protein structures:
Pfam  structures / ECOD  
PDBRCSB PDB; PDBe; PDBj
PDBsumstructure summary
PDB1FBQ​, 1FBS​, 1FBU​, 1FYK​, 1FYL​, 1FYM​, 1HKS​, 1HKT​, 2HTS​, 3HSF​, 3HTS​
Vertebrate heat shock transcription factor
Identifiers
SymbolVert_HS_TF
PfamPF06546
InterProIPR010542
Available protein structures:
Pfam  structures / ECOD  
PDBRCSB PDB; PDBe; PDBj
PDBsumstructure summary

Function

Heat shock factors (HSF) are transcriptional activators of heat shock genes.[3] These activators bind specifically to Heat Shock sequence Elements (HSE) throughout the genome[4] whose consensus-sequence is a tandem array of three oppositely oriented "AGAAN" motifs or a degenerate version thereof. Under non-stressed conditions, Drosophila HSF is a nuclear-localized unbound monomer, whereas heat shock activation results in trimerization and binding to the HSE.[5] The Heat Shock sequence Element is highly conserved from yeast to humans.[6]

Heat shock factor 1 (HSF-1) is the major regulator of heat shock protein transcription in eukaryotes. In the absence of cellular stress, HSF-1 is inhibited by association with heat shock proteins and is therefore not active. Cellular stresses, such as increased temperature, can cause proteins in the cell to misfold. Heat shock proteins bind to the misfolded proteins and dissociate from HSF-1. This allows HSF1 to form trimers and translocate to the cell nucleus and activate transcription.[7] Its function is not only critical to overcome the proteotoxic effects of thermal stress, but also needed for proper animal development and the overall survival of cancer cells.[8][9]

Structure

Each HSF monomer contains one C-terminal and three N-terminal leucine zipper repeats.[10] Point mutations in these regions result in disruption of cellular localisation, rendering the protein constitutively nuclear in humans.[5] Two sequences flanking the N-terminal zippers fit the consensus of a bi-partite nuclear localization signal (NLS). Interaction between the N- and C-terminal zippers may result in a structure that masks the NLS sequences: following activation of HSF, these may then be unmasked, resulting in relocalisation of the protein to the nucleus.[10] The DNA-binding component of HSF lies to the N-terminus of the first NLS region, and is referred to as the HSF domain.

Isoforms

Humans express the following heat shock factors:

gene protein
HSF1 heat shock transcription factor 1
HSF2 heat shock transcription factor 2
HSF2BP heat shock transcription factor 2 binding protein
HSF4 heat shock transcription factor 4
HSF5 heat shock transcription factor family member 5
HSFX1 heat shock transcription factor family, X linked 1
HSFX2 heat shock transcription factor family, X linked 2
HSFY1 heat shock transcription factor, Y-linked 1
HSFY2 heat shock transcription factor, Y-linked 2

See also

References
  1. Sorger PK (May 1991). "Heat shock factor and the heat shock response". Cell. 65 (3): 363–6. doi:10.1016/0092-8674(91)90452-5. PMID 2018972. S2CID 5169812.
  2. Morimoto RI (March 1993). "Cells in stress: transcriptional activation of heat shock genes". Science. 259 (5100): 1409–10. Bibcode:1993Sci...259.1409M. doi:10.1126/science.8451637. PMID 8451637.
  3. Clos J, Westwood JT, Becker PB, Wilson S, Lambert K, Wu C (November 1990). "Molecular cloning and expression of a hexameric Drosophila heat shock factor subject to negative regulation". Cell. 63 (5): 1085–97. doi:10.1016/0092-8674(90)90511-C. PMID 2257625. S2CID 205020185.
  4. Guertin MJ, Lis JT (September 2010). "Chromatin landscape dictates HSF binding to target DNA elements". PLOS Genet. 6 (9): e1001114. doi:10.1371/journal.pgen.1001114. PMC 2936546. PMID 20844575.
  5. Rabindran SK, Giorgi G, Clos J, Wu C (August 1991). "Molecular cloning and expression of a human heat shock factor, HSF1". Proc. Natl. Acad. Sci. U.S.A. 88 (16): 6906–10. Bibcode:1991PNAS...88.6906R. doi:10.1073/pnas.88.16.6906. PMC 52202. PMID 1871105.
  6. Guertin MJ, Petesch SJ, Zobeck KL, Min IM, Lis JT (2010). "Drosophila heat shock system as a general model to investigate transcriptional regulation". Cold Spring Harb. Symp. Quant. Biol. 75: 1–9. doi:10.1101/sqb.2010.75.039. PMC 5967404. PMID 21467139.
  7. Prahlad V, Morimoto RI (February 2009). "Integrating the stress response: lessons for neurodegenerative diseases from C. elegans". Trends Cell Biol. 19 (2): 52–61. doi:10.1016/j.tcb.2008.11.002. PMC 4843516. PMID 19112021.
  8. Salamanca HH, Fuda N, Shi H, Lis JT (August 2011). "An RNA aptamer perturbs heat shock transcription factor activity in Drosophila melanogaster". Nucleic Acids Res. 39 (15): 6729–40. doi:10.1093/nar/gkr206. PMC 3159435. PMID 21576228.
  9. Salamanca HH, Antonyak MA, Cerione RA, Shi H, Lis JT (2014). "Inhibiting heat shock factor 1 in human cancer cells with a potent RNA aptamer". PLOS ONE. 9 (5): e96330. Bibcode:2014PLoSO...996330S. doi:10.1371/journal.pone.0096330. PMC 4011729. PMID 24800749.
  10. Schuetz TJ, Gallo GJ, Sheldon L, Tempst P, Kingston RE (August 1991). "Isolation of a cDNA for HSF2: evidence for two heat shock factor genes in humans". Proc. Natl. Acad. Sci. U.S.A. 88 (16): 6911–5. Bibcode:1991PNAS...88.6911S. doi:10.1073/pnas.88.16.6911. PMC 52203. PMID 1871106.
This article incorporates text from the public domain Pfam and InterPro: IPR000232
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