Evidence map›Paper›PMID 27052732›Full record

ArticleMolecular cell2016

Mammalian Heat Shock Response and Mechanisms Underlying Its Genome-wide Transcriptional Regulation.

Dig B Mahat, H Hans Salamanca, Fabiana M Duarte, Charles G Danko, John T Lis

Open access · bronzeAbstract read
In one paragraph

Article in Molecular cell, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 260 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
260citing papers in PubMed, 1 pooled it
21.9field-weighted citation impact, top 1% 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

260 citing papers in PubMed, 1 synthesis or guideline pooled it, 445 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. More than the 'master regulator of cytosolic proteostasis': new roles for HSF1 in promoting tissue health.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2026
    Review
  5. Adaptation to heat stress by diversification of the vertebrate heat shock transcription factor family.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2026
    Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Review
  11. Review
  12. Re-Evaluating Hot Mitochondria: Too Slow to Cool.Acta physiologica (Oxford, England) · 2026
    Review
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Traceless Regulation of Genetic Circuitry.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Review
  19. Article
  20. Article

200 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 1 institution in 1 country.

Dig B MahatDepartment of Molecular Biology and Genetics, Cornell University, Ithaca, New York 14850, USA.
H Hans SalamancaDepartment of Molecular Biology and Genetics, Cornell University, Ithaca, New York 14850, USA.
Fabiana M DuarteDepartment of Molecular Biology and Genetics, Cornell University, Ithaca, New York 14850, USA.
Charles G DankoBaker Institute for Animal Health, Cornell University, Ithaca, New York 14850, USA.
John T LisDepartment of Molecular Biology and Genetics, Cornell University, Ithaca, New York 14850, USA. Electronic address: jtl10@cornell.edu.
Cornell University · US

Funding

COORDINATE GENE REGULATION IN ANIMAL CELLSR01GM025232 · NIGMS · CORNELL UNIVERSITY ITHACA · PI LIS, JOHN T · 1985 to 2020
$8.4M
NIGMS NIH HHS R01 GM025232NIGMS NIH HHS R01GM25232
6 · The paper itself

Abstract

The heat shock response (HSR) is critical for survival of all organisms. However, its scope, extent, and the molecular mechanism of regulation are poorly understood. Here we show that the genome-wide transcriptional response to heat shock in mammals is rapid and dynamic and results in induction of several hundred and repression of several thousand genes. Heat shock factor 1 (HSF1), the "master regulator" of the HSR, controls only a fraction of heat shock-induced genes and does so by increasing RNA polymerase II release from promoter-proximal pause. Notably, HSF2 does not compensate for the lack of HSF1. However, serum response factor appears to transiently induce cytoskeletal genes independently of HSF1. The pervasive repression of transcription is predominantly HSF1-independent and is mediated through reduction of RNA polymerase II pause release. Overall, mammalian cells orchestrate rapid, dynamic, and extensive changes in transcription upon heat shock that are largely modulated at pause release, and HSF1 plays a limited and specialized role.

Indexed as

Heat-Shock ResponseTranscription, GeneticAnimalsCell LineDNA-Binding ProteinsFibroblastsGene Expression RegulationHeat-Shock ProteinsHeat Shock Transcription FactorsMammalsMicePromoter Regions, GeneticRNA Polymerase IISerum Response FactorTranscription FactorsDNA-Binding ProteinsHeat-Shock ProteinsHeat Shock Transcription FactorsHsf1 protein, mouseHsf2 protein, mouseRNA Polymerase IISerum Response FactorTranscription Factors

Identifiers

PMID27052732
PMCPMC4826300
OpenAlexW2306540679

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.