Evidence map›Paper›PMID 20156966›Full record

ArticleThe Journal of cell biology2010

BAG1 restores formation of functional DJ-1 L166P dimers and DJ-1 chaperone activity.

Sebastian Deeg, Mathias Gralle, Kamila Sroka, Mathias Bähr, Fred Silvester Wouters, Pawel Kermer

Open access · hybridAbstract read
In one paragraph

Article in The Journal of cell biology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

20 citing papers in PubMed, 41 citations in OpenAlex.

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  14. SUMO and Parkinson's disease.Neuromolecular medicine · 2013
    Review
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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

6 authors at 2 institutions in 1 country.

Sebastian DeegDepartment for Neurology, Georg-August University Göttingen, 37073 Göttingen, Germany.
Mathias Gralle
Kamila Sroka
Mathias Bähr
Fred Silvester Wouters
Pawel Kermer
Deutsche Forschungsgemeinschaft · DEUniversity of Göttingen · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mutations in the gene coding for DJ-1 protein lead to early-onset recessive forms of Parkinson's disease. It is believed that loss of DJ-1 function is causative for disease, although the function of DJ-1 still remains a matter of controversy. We show that DJ-1 is localized in the cytosol and is associated with membranes and organelles in the form of homodimers. The disease-related mutation L166P shifts its subcellular distribution to the nucleus and decreases its ability to dimerize, impairing cell survival. Using an intracellular foldase biosensor, we found that wild-type DJ-1 possesses chaperone activity, which is abolished by the L166P mutation. We observed that this aberrant phenotype can be reversed by the expression of the cochaperone BAG1 (Bcl-2-associated athanogene 1), restoring DJ-1 subcellular distribution, dimer formation, and chaperone activity and ameliorating cell survival.

Indexed as

Protein MultimerizationAmino Acid SubstitutionCell DeathCell LineDNA-Binding ProteinsHumansImmunoprecipitationIntracellular Signaling Peptides and ProteinsMolecular ChaperonesMutant ProteinsOncogene ProteinsProtein BindingProtein Deglycase DJ-1Protein TransportRecombinant ProteinsSubcellular FractionsBCL2-associated athanogene 1 proteinDNA-Binding ProteinsIntracellular Signaling Peptides and ProteinsMolecular ChaperonesMutant ProteinsOncogene ProteinsPARK7 protein, humanProtein Deglycase DJ-1Recombinant ProteinsTranscription Factors

Identifiers

PMID20156966
PMCPMC2828921
OpenAlexW2127020153

What OpenQuestion holds

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LicenceCC BY-NC-SA
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.