Evidence map›Paper›PMID 41230889›Full record

ArticlePlant physiology2025

Promoter and domain swap analysis delineates heat stress memory-specific determinants of heat shock factor HSFA2.

Vicky Oberkofler, Joan Baltzer, Witold Szymanski, Isabel Bäurle

Abstract read
In one paragraph

Article in Plant physiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Article
  2. Principles and mechanisms of plant acclimation to heat stress.Nature reviews. Molecular cell biology · 2026
    Review
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  4. Article
4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Vicky OberkoflerInstitute for Biochemistry and Biology, University of Potsdam, 14476 Potsdam, Germany.ORCID 0000-0001-6884-147X
Joan BaltzerInstitute for Biochemistry and Biology, University of Potsdam, 14476 Potsdam, Germany.ORCID 0009-0005-5681-2088
Witold SzymanskiInstitute of Translational Proteomics, Biochemical/Pharmacological Center, Philipps University, 35043 Marburg, Germany.ORCID 0000-0002-1202-3299
Isabel BäurleInstitute for Biochemistry and Biology, University of Potsdam, 14476 Potsdam, Germany.ORCID 0000-0001-5633-8068

Funding

European Research Council 725295
6 · The paper itself

Abstract

Exposure to moderate heat stress (HS) primes plants to better withstand future exposure to more severe HS conditions. In Arabidopsis (Arabidopsis thaliana), the primed state is maintained for several days, referred to as HS memory. HEAT SHOCK TRANSCRIPTION FACTOR A2 (HSFA2) and HSFA3 promote this HS memory by jointly mediating transcriptional memory in a subset of HS-inducible genes. Why only 2 of the 21 HSFs in Arabidopsis function specifically in HS memory is unknown. Here, we investigated this question through a promoter and domain swap analysis between HSFA2 and HSFA1D, a regulator of the acute HS response (HSR), aiming to uncover the requirements for HS memory HSFs. We determined that conferring the expression pattern of HSFA2 to HSFA1D is not sufficient for restoring HS memory. In chimeric proteins, the C-terminal regions and the DNA-binding domains (DBDs) of the 2 HSFs are interchangeable, while the presence of the HSFA1D repression domain abrogates HS memory. Interestingly, the oligomerization domain (OD) of HSFA1D cannot replace its HSFA2 counterpart in mediating physiological HS memory, suggesting a role for distinct interacting HSF complexes. The OD-exchanged chimeric HSF hyper-induced memory genes after a single HS, suggesting an altered response of the protein to HS. In summary, our study provides insights into the roles of individual HSF domains in specifying functions in HS memory or the acute HSR, thus providing avenues for tailoring HSFs to the demands of a changing climate.

Indexed as

ArabidopsisArabidopsis ProteinsHeat-Shock ResponseHeat Shock Transcription FactorsPromoter Regions, GeneticTranscription FactorsGene Expression Regulation, PlantPlants, Genetically ModifiedProtein DomainsArabidopsis ProteinsHeat Shock Transcription FactorsHSFA2 protein, ArabidopsisTranscription Factors

Identifiers

PMID41230889
PMCPMC12646075

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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.