Evidence map›Paper›PMID 33894203›Full record

ArticleThe Journal of biological chemistry

Tolerance to nascent protein misfolding stress requires fine-tuning of the cAMP/PKA pathway.

Paraskevi Kritsiligkou, Karol Nowicki-Osuch, Zorana Carter, Chris J Kershaw, Declan R Creamer, Alan J Weids, Chris M Grant

Open access · goldAbstract read
In one paragraph

Article in The Journal of biological chemistry. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.0field-weighted citation impact, top 29% 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

8 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Article
  3. Cytosolic PeroxiredoxinJournal of agricultural and food chemistry · 2025
    Article
  4. Review
  5. Review
  6. Review
  7. Review
  8. 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

7 authors at 2 institutions in 1 country.

Paraskevi KritsiligkouFaculty of Biology, Medicine and Health, The University of Manchester, Manchester, UK. Electronic address: p.kritsiligkou@dkfz-heidelberg.de.
Karol Nowicki-OsuchFaculty of Biology, Medicine and Health, The University of Manchester, Manchester, UK.
Zorana CarterFaculty of Biology, Medicine and Health, The University of Manchester, Manchester, UK.
Chris J KershawFaculty of Biology, Medicine and Health, The University of Manchester, Manchester, UK.
Declan R CreamerFaculty of Biology, Medicine and Health, The University of Manchester, Manchester, UK.
Alan J WeidsFaculty of Biology, Medicine and Health, The University of Manchester, Manchester, UK.
Chris M GrantFaculty of Biology, Medicine and Health, The University of Manchester, Manchester, UK. Electronic address: chris.grant@manchester.ac.uk.
University of Manchester · GBManchester Academic Health Science Centre · GB

Funding

Wellcome Trust
6 · The paper itself

Abstract

Protein aggregation is the abnormal association of misfolded proteins into larger, often insoluble structures that can be toxic during aging and in protein aggregation-associated diseases. Previous research has established a role for the cytosolic Tsa1 peroxiredoxin in responding to protein misfolding stress. Tsa1 is also known to downregulate the cAMP/protein kinase A (PKA) pathway as part of the response to hydrogen peroxide stress. However, whether the cAMP/PKA pathway is involved in protein misfolding stress is not known. Using transcriptomics, we examined the response to protein misfolding stress and found upregulation of numerous stress gene functions and downregulation of many genes related to protein synthesis and other growth-related processes consistent with the well-characterized environmental stress response. The scope of the transcriptional response is largely similar in wild-type and tsa1 mutant strains, but the magnitude is dampened in the strain lacking Tsa1. We identified a direct protein interaction between Tsa1 and the Bcy1 regulatory subunit of PKA that is present under normal growth conditions and explains the observed differences in gene expression profiles. This interaction is increased in a redox-dependent manner in response to nascent protein misfolding, via Tsa1-mediated oxidation of Bcy1. Oxidation of Bcy1 causes a reduction in cAMP binding by Bcy1, which dampens PKA pathway activity, leading to a targeted reprogramming of gene expression. Redox regulation of the regulatory subunit of PKA provides a mechanism to mitigate the toxic consequences of protein misfolding stress that is distinct to stress caused by exogenous sources of reactive oxygen species.

Indexed as

Protein FoldingStress, PhysiologicalCyclic AMPCyclic AMP-Dependent Protein KinasesGene Expression ProfilingMutationProtein AggregatesSaccharomyces cerevisiaeCyclic AMPCyclic AMP-Dependent Protein KinasesProtein Aggregatescell signalinggene expressionhydrogen peroxideoxidation–reduction (redox)oxidative stressperoxiredoxinprotein kinase A (PKA)protein misfoldingstress responseyeast

Identifiers

PMID33894203
PMCPMC8164027
OpenAlexW3155850780

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.