Evidence map›Paper›PMID 25688804›Full record

ArticleJournal of molecular biology2015

Lysine deacetylases regulate the heat shock response including the age-associated impairment of HSF1.

Elena Zelin, Brian C Freeman

Abstract read
In one paragraph

Article in Journal of molecular biology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
3.0field-weighted citation impact, top 9% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

37 citing papers in PubMed, 53 citations in OpenAlex.

  1. Proteostasis and ageing dissidence.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2026
    Review
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. HSF1 and Its Role in Huntington's Disease Pathology.Advances in experimental medicine and biology · 2023
    Review
  10. Review
  11. Article
  12. Article
  13. Classic and exertional heatstroke.Nature reviews. Disease primers · 2022
    Review
  14. Article
  15. Heat Shock Proteins and HSF1 in Cancer.Frontiers in oncology · 2022
    Review
  16. The heat shock response and small molecule regulators.European journal of medicinal chemistry · 2021
    Review
  17. Article
  18. Mechanisms of TDP-43 Proteinopathy Onset and Propagation.International journal of molecular sciences · 2021
    Review
  19. Review
  20. Cellular proteostasis decline in human senescence.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors at 1 institution in 1 country.

Elena ZelinDepartment of Cell and Developmental Biology, University of Illinois at Urbana-Champaign, 601 South Goodwin Avenue, Urbana, IL 61801, USA.
Brian C FreemanDepartment of Cell and Developmental Biology, University of Illinois at Urbana-Champaign, 601 South Goodwin Avenue, Urbana, IL 61801, USA. Electronic address: bfree@illinois.edu.
University of Illinois Urbana-Champaign · US

Funding

The Hsp90 molecular chaperone systemR01CA155333 · NCI · UNIVERSITY OF ILLINOIS AT URBANA-CHAMPAIGN · PI FREEMAN, BRIAN C · 2011 to 2015
$1.5M
NCI NIH HHS CA155333NCI NIH HHS R01 CA155333
6 · The paper itself

Abstract

Heat shock factor 1 (HSF1) is critical for defending cells from both acute and chronic stresses. In aging cells, the DNA binding activity of HSF1 deteriorates correlating with the onset of pathological events including neurodegeneration and heart disease. We find that DNA binding by HSF1 is controlled by lysine deacetylases with HDAC7, HDAC9, and SIRT1 distinctly increasing the magnitude and length of a heat shock response (HSR). In contrast, HDAC1 inhibits HSF1 in a deacetylase-independent manner. In aging cells, the levels of HDAC1 are elevated and the HSR is impaired, yet reduction of HDAC1 in aged cells restores the HSR. Our results provide a mechanistic basis for the age-associated regulation of the HSR. Besides HSF1, the deacetylases differentially modulate the activities of unrelated DNA binding proteins. Taken together, our data further support the model that lysine deacetylases are selective regulators of DNA binding proteins.

Indexed as

Heat-Shock ResponseAcetylationAnimalsCells, CulturedCellular SenescenceDNA-Binding ProteinsHeat Shock Transcription FactorsHEK293 CellsHeLa CellsHistone Deacetylase 1HumansLysineMicep300-CBP-Associated Factorp300-CBP Transcription FactorsTranscription FactorsDNA-Binding ProteinsHeat Shock Transcription FactorsHistone Deacetylase 1HSF1 protein, humanLysinep300-CBP-Associated Factorp300-CBP Transcription FactorsTranscription Factorsagingheat shock factor 1heat shock responselysine deacetylase

Identifiers

PMID25688804
PMCPMC4357550
OpenAlexW2002852563

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.