Evidence map›Paper›PMID 34964690›Full record

ArticleAutophagy2022

Converging roles of PSENEN/PEN2 and CLN3 in the autophagy-lysosome system.

Marcel Klein, Abuzar Kaleem, Sandra Oetjen, Daniela Wünkhaus, Lars Binkle, Sandra Schilling, Milena Gjorgjieva, Ralf Scholz, Doris Gruber-Schoffnegger, Stephan Storch and 5 more

Open access · bronzeAbstract read
In one paragraph

Article in Autophagy, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

9 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
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  7. A HomozygousGenes · 2023
    Article
  8. Review
  9. Functions and mechanisms of cytosolic phospholipase ANeural regeneration research · 2023
    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

15 authors at 3 institutions in 1 country.

Marcel KleinInstitute for Molecular and Cellular Cognition, Center for Molecular Neurobiology Hamburg, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Abuzar KaleemInstitute for Molecular and Cellular Cognition, Center for Molecular Neurobiology Hamburg, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Sandra OetjenInstitute for Molecular and Cellular Cognition, Center for Molecular Neurobiology Hamburg, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Daniela WünkhausEvotec SE, Manfred Eigen Campus, Hamburg, Germany.
Lars BinkleInstitute of Neuroimmunology and Multiple Sclerosis, Center for Molecular Neurobiology Hamburg, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Sandra SchillingDivision of Human Biology and Human Genetics, University of Kaiserslautern, Kaiserslautern, Germany.
Milena GjorgjievaInstitute for Molecular and Cellular Cognition, Center for Molecular Neurobiology Hamburg, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Ralf ScholzInstitute for Molecular and Cellular Cognition, Center for Molecular Neurobiology Hamburg, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Doris Gruber-SchoffneggerEvotec SE, Manfred Eigen Campus, Hamburg, Germany.
Stephan StorchDepartment of Pediatrics, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Stefan KinsDivision of Human Biology and Human Genetics, University of Kaiserslautern, Kaiserslautern, Germany.
Gerard DrewesCellzome, Functional Genomics Research and Development, Heidelberg, Germany.
Sabine Hoffmeister-UllerichBioanalytics, Center for Molecular Neurobiology Hamburg, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Dietmar KuhlInstitute for Molecular and Cellular Cognition, Center for Molecular Neurobiology Hamburg, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Guido HermeyInstitute for Molecular and Cellular Cognition, Center for Molecular Neurobiology Hamburg, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.ORCID 0000-0003-4762-5262
Universität Hamburg · DEEvotec (Germany) · DEUniversity of Kaiserslautern · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PSENEN/PEN2 is the smallest subunit of the γ-secretase complex, an intramembrane protease that cleaves proteins within their transmembrane domains. Mutations in components of the γ-secretase underlie familial Alzheimer disease. In addition to its proteolytic activity, supplementary, γ-secretase independent, functions in the macroautophagy/autophagy-lysosome system have been proposed. Here, we screened for PSENEN-interacting proteins and identified CLN3. Mutations in

Indexed as

Alzheimer DiseaseNeuronal Ceroid-LipofuscinosesAmyloid Precursor Protein SecretasesAutophagyChildHumansLysosomesMembrane GlycoproteinsMembrane ProteinsMolecular ChaperonesPresenilinsTranscription FactorsAmyloid Precursor Protein SecretasesCLN3 protein, humanMembrane GlycoproteinsMembrane ProteinsMolecular ChaperonesPresenilinsPSENEN protein, humanTranscription FactorsAlzheimer diseasecln3 diseaseknockout cellsneuronal ceroid lipofuscinosistranscription factor ebγ-secretase

Identifiers

PMID34964690
PMCPMC9397472
OpenAlexW4200390887

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.