Evidence map›Paper›PMID 35729039›Full record

ReviewTrends in cell biology2023

J-domain protein chaperone circuits in proteostasis and disease.

Ruobing Zhang, Duccio Malinverni, Douglas M Cyr, Paolo De Los Rios, Nadinath B Nillegoda

Open access · greenAbstract readReview
In one paragraph

Review in Trends in cell biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
5.1field-weighted citation impact, top 3% 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

44 citing papers in PubMed, 61 citations in OpenAlex.

  1. 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
  2. Article
  3. Review
  4. Human Hsp70 paralogs display selective J-domain interactions tuning proteostasis under stress.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  5. Article
  6. DNAJB6: A guardian against neurodegeneration.Neural regeneration research · 2026
    Article
  7. Article
  8. Article
  9. Article
  10. Mechanisms and regulation of the Hsp70 chaperone network.Nature reviews. Molecular cell biology · 2026
    Review
  11. Origin of class B J-domain proteins involved in amyloid transactions.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  12. Review
  13. Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. A pentatomomorpha-specific salivary protein activates plant immunity and is critical for insect feeding.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  20. Review
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

5 authors at 4 institutions in 4 countries.

Ruobing ZhangAustralian Regenerative Medicine Institute (ARMI), Monash University, Melbourne, Victoria, Australia.
Duccio MalinverniMRC Laboratory of Molecular Biology, Cambridge, UK; Department of Structural Biology and Center for Data Driven Discovery, St Jude Children's Research Hospital, Memphis, TN, USA.
Douglas M CyrDepartment of Cell Biology and Physiology and the Cystic Fibrosis/Pulmonary Research and Treatment Center, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.
Paolo De Los RiosInstitute of Physics, School of Basic Sciences and Institute of Bioengineering, School of Life Sciences, École Polytechnique Fédérale de Lausanne (EPFL), Lausanne, Switzerland.
Nadinath B NillegodaAustralian Regenerative Medicine Institute (ARMI), Monash University, Melbourne, Victoria, Australia. Electronic address: nadinath.nillegoda@monash.edu.
Australian Regenerative Medicine Institute · AUÉcole Polytechnique Fédérale de Lausanne · CHSt. Jude Children's Research Hospital · USUniversity of North Carolina at Chapel Hill · US

Funding

Roles for Hsp70 and Hsp40 in Membrane Protein TriageR01GM056981 · NIGMS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI CYR, DOUGLAS M · 1998 to 2019
$6.1M
Hsp40 and Hsp70 in Membrane Protein TriageR01GM151501 · NIGMS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI DOUGLAS M CYR · 2023 to 2026
$1.7M
Medical Research Council MC_U105185859NIGMS NIH HHS R01 GM056981NIGMS NIH HHS R01 GM151501
6 · The paper itself

Abstract

The J-domain proteins (JDP) form the largest protein family among cellular chaperones. In cooperation with the Hsp70 chaperone system, these co-chaperones orchestrate a plethora of distinct functions, including those that help maintain cellular proteostasis and development. JDPs evolved largely through the fusion of a J-domain with other protein subdomains. The highly conserved J-domain facilitates the binding and activation of Hsp70s. How JDPs (re)wire Hsp70 chaperone circuits and promote functional diversity remains insufficiently explained. Here, we discuss recent advances in our understanding of the JDP family with a focus on the regulation built around J-domains to ensure correct pairing and assembly of JDP-Hsp70 machineries that operate on different clientele under various cellular growth conditions.

Indexed as

HSP40 Heat-Shock ProteinsProteostasisHSP70 Heat-Shock ProteinsHumansMolecular ChaperonesProtein BindingHSP40 Heat-Shock ProteinsHSP70 Heat-Shock ProteinsMolecular ChaperonesHsp40Hsp70J-domainJ-domain proteinsprotein conformational diseasesprotein homeostasis

Identifiers

PMID35729039
PMCPMC9759622
OpenAlexW4283123783

What Socratic 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 Socratic graph.