Literature DB >> 1936996

Attenuation of the heat shock response in HeLa cells is mediated by the release of bound heat shock transcription factor and is modulated by changes in growth and in heat shock temperatures.

K Abravaya1, B Phillips, R I Morimoto.   

Abstract

When HeLa S3 cells are subjected to a continuous 42 degrees C heat shock, activation of heat shock transcription factor (HSF) and transcriptional activation of the heat shock genes hsp70, hsp89 alpha, and hsp60 is transient, peaking at 40-60 min of heat shock, and then attenuating. We have used in vivo genomic footprinting to demonstrate that attenuation of hsp70 transcription is mediated by release of bound HSF from the heat shock element (HSE) of the hsp70 gene promoter. Release of bound HSF in vivo occurs at a higher rate than would be predicted from in vitro measurements of dissociation. Attenuation of HSF activation and heat shock gene transcription occurs only when mild heat shock temperatures are employed (42 degrees C); increasing the heat shock temperature by 1 degree C elicits a much higher level of activation, which does not attenuate during a 4-hr heat shock. Surprisingly, altering the temperature at which cells are grown prior to heat shock modulates the magnitude and temporal pattern of the response to a given heat shock temperature. This finding suggests that HSF does not sense temperature directly but, instead, may be responsive to the magnitude of the difference between growth and heat shock temperatures.

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Year:  1991        PMID: 1936996     DOI: 10.1101/gad.5.11.2117

Source DB:  PubMed          Journal:  Genes Dev        ISSN: 0890-9369            Impact factor:   11.361


  61 in total

1.  Short-term hyperthermia prevents activation of proinflammatory genes in fibroblast-like synoviocytes by blocking the activation of the transcription factor NF-kappaB.

Authors:  Marica Markovic; Karl M Stuhlmeier
Journal:  J Mol Med (Berl)       Date:  2006-09-06       Impact factor: 4.599

Review 2.  Transcellular chaperone signaling: an organismal strategy for integrated cell stress responses.

Authors:  Patricija van Oosten-Hawle; Richard I Morimoto
Journal:  J Exp Biol       Date:  2014-01-01       Impact factor: 3.312

3.  Molecular chaperones as HSF1-specific transcriptional repressors.

Authors:  Y Shi; D D Mosser; R I Morimoto
Journal:  Genes Dev       Date:  1998-03-01       Impact factor: 11.361

4.  The proteasome inhibitor bortezomib is a potent inducer of zinc finger AN1-type domain 2a gene expression: role of heat shock factor 1 (HSF1)-heat shock factor 2 (HSF2) heterocomplexes.

Authors:  Antonio Rossi; Anna Riccio; Marta Coccia; Edoardo Trotta; Simone La Frazia; M Gabriella Santoro
Journal:  J Biol Chem       Date:  2014-03-11       Impact factor: 5.157

5.  Near-infrared optogenetic engineering of photothermal nanoCRISPR for programmable genome editing.

Authors:  Xiaohong Chen; Yuxuan Chen; Huhu Xin; Tao Wan; Yuan Ping
Journal:  Proc Natl Acad Sci U S A       Date:  2020-01-15       Impact factor: 11.205

6.  Characterization of constitutive HSF2 DNA-binding activity in mouse embryonal carcinoma cells.

Authors:  S P Murphy; J J Gorzowski; K D Sarge; B Phillips
Journal:  Mol Cell Biol       Date:  1994-08       Impact factor: 4.272

7.  Focused cerebellar laser light induced hyperthermia improves symptoms and pathology of polyglutamine disease SCA1 in a mouse model.

Authors:  Scoty M Hearst; Qingmei Shao; Mariper Lopez; Drazen Raucher; Parminder J S Vig
Journal:  Cerebellum       Date:  2014-10       Impact factor: 3.847

Review 8.  Molecular parameters of hyperthermia for radiosensitization.

Authors:  Tej K Pandita; Shruti Pandita; Sukesh R Bhaumik
Journal:  Crit Rev Eukaryot Gene Expr       Date:  2009       Impact factor: 1.807

9.  The DNA-binding activity of the human heat shock transcription factor is regulated in vivo by hsp70.

Authors:  D D Mosser; J Duchaine; B Massie
Journal:  Mol Cell Biol       Date:  1993-09       Impact factor: 4.272

10.  Glycogen synthase kinase 3beta and extracellular signal-regulated kinase inactivate heat shock transcription factor 1 by facilitating the disappearance of transcriptionally active granules after heat shock.

Authors:  B He; Y H Meng; N F Mivechi
Journal:  Mol Cell Biol       Date:  1998-11       Impact factor: 4.272

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