Evidence map›Paper›PMID 36624536›Full record

ArticleActa neuropathologica communications2023

Differential effects of mutations of POPDC proteins on heteromeric interaction and membrane trafficking.

Alexander H Swan, Roland F R Schindler, Marco Savarese, Isabelle Mayer, Susanne Rinné, Felix Bleser, Anne Schänzer, Andreas Hahn, Mario Sabatelli, Francesco Perna and 7 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Acta neuropathologica communications, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.7field-weighted citation impact, top 17% 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

4 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Article
  3. Genes · 2024
    Article
  4. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

17 authors at 10 institutions in 5 countries.

Alexander H SwanNational Heart and Lung Institute (NHLI), Imperial College London, London, UK.ORCID http://orcid.org/0000-0003-2177-8703
Roland F R SchindlerNational Heart and Lung Institute (NHLI), Imperial College London, London, UK.ORCID http://orcid.org/0000-0001-6823-9622
Marco SavareseDepartment of Medical Genetics, Medicum, University of Helsinki, Helsinki, Finland.ORCID http://orcid.org/0000-0002-2591-244X
Isabelle MayerNational Heart and Lung Institute (NHLI), Imperial College London, London, UK.
Susanne RinnéInstitute for Physiology and Pathophysiology, Vegetative Physiology, Philipps-University of Marburg, Marburg, Germany.ORCID http://orcid.org/0000-0003-2326-7069
Felix BleserInstitute for Physiology and Pathophysiology, Vegetative Physiology, Philipps-University of Marburg, Marburg, Germany.
Anne SchänzerInstitute of Neuropathology, Justus Liebig University Giessen, Giessen, Germany.ORCID http://orcid.org/0000-0002-2014-2028
Andreas HahnDepartment of Child Neurology, Justus Liebig University Giessen, Giessen, Germany.ORCID http://orcid.org/0000-0003-0235-5211
Mario SabatelliDepartment of Neurology, Universitá Cattolica del Sacro Cuore, Rome, Italy.ORCID http://orcid.org/0000-0001-6635-4985
Francesco PernaDipartimento Di Scienze Cardiovascolari, Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy.ORCID http://orcid.org/0000-0002-9019-9492
Kathryn ChapmanAssay Biology, Domainex Ltd, Cambridge, CB10 1XL, UK.
Mark PfuhlSchool of Cardiovascular Medicine and Sciences and Randall Centre, King's College London, London, UK.ORCID http://orcid.org/0000-0001-9592-6639
Alan C SpiveyDepartment of Chemistry, Imperial College London, London, UK.ORCID http://orcid.org/0000-0001-5114-490X
Niels DecherInstitute for Physiology and Pathophysiology, Vegetative Physiology, Philipps-University of Marburg, Marburg, Germany.ORCID http://orcid.org/0000-0002-9433-687X
Bjarne UddFolkhälsan Research Center, University of Helsinki, Helsinki, Finland.ORCID http://orcid.org/0000-0002-1101-9730
Giorgio TascaUnità Operativa Complessa di Neurologia, Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy.ORCID http://orcid.org/0000-0003-0849-9144
Thomas BrandNational Heart and Lung Institute (NHLI), Imperial College London, London, UK. t.brand@imperial.ac.uk.ORCID http://orcid.org/0000-0001-7090-5356
Imperial College London · GBPhilipps University of Marburg · DEDomainex (United Kingdom) · GBJustus-Liebig-Universität Gießen · DEUniversity of Helsinki · FIAgostino Gemelli University Polyclinic · ITKing's College London · GBLung Institute · USNewcastle upon Tyne Hospitals NHS Foundation Trust · GBUniversità Cattolica del Sacro Cuore · IT

Funding

British Heart Foundation PG/14/46/30911British Heart Foundation PG/19/13/34247
6 · The paper itself

Abstract

The Popeye domain containing (POPDC) genes encode sarcolemma-localized cAMP effector proteins. Mutations in blood vessel epicardial substance (BVES) also known as POPDC1 and POPDC2 have been associated with limb-girdle muscular dystrophy and cardiac arrhythmia. Muscle biopsies of affected patients display impaired membrane trafficking of both POPDC isoforms. Biopsy material of patients carrying mutations in BVES were immunostained with POPDC antibodies. The interaction of POPDC proteins was investigated by co-precipitation, proximity ligation, bioluminescence resonance energy transfer and bimolecular fluorescence complementation. Site-directed mutagenesis was utilised to map the domains involved in protein-protein interaction. Patients carrying a novel homozygous variant, BVES (c.547G > T, p.V183F) displayed only a skeletal muscle pathology and a mild impairment of membrane trafficking of both POPDC isoforms. In contrast, variants such as BVES p.Q153X or POPDC2 p.W188X were associated with a greater impairment of membrane trafficking. Co-transfection analysis in HEK293 cells revealed that POPDC proteins interact with each other through a helix-helix interface located at the C-terminus of the Popeye domain. Site-directed mutagenesis of an array of ultra-conserved hydrophobic residues demonstrated that some of them are required for membrane trafficking of the POPDC1-POPDC2 complex. Mutations in POPDC proteins that cause an impairment in membrane localization affect POPDC complex formation while mutations which leave protein-protein interaction intact likely affect some other essential function of POPDC proteins.

Indexed as

AntibodiesMuscle ProteinsBiopsyCell Adhesion MoleculesHEK293 CellsHomozygoteHumansMutationAntibodiesCell Adhesion MoleculesMuscle ProteinsPOPDC1 protein, humanCyclic nucleotide binding domainLimb-girdle muscular dystrophyMembrane traffickingMutationPopeye domainProtein–protein interactionα-helix

Identifiers

PMID36624536
PMCPMC9830914
OpenAlexW4315436368

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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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 Socratic graph.