Evidence map›Paper›PMID 32130108›Full record

ArticleeLife2020

Proteome profile of peripheral myelin in healthy mice and in a neuropathy model.

Sophie B Siems, Olaf Jahn, Maria A Eichel, Nirmal Kannaiyan, Lai Man N Wu, Diane L Sherman, Kathrin Kusch, Dörte Hesse, Ramona B Jung, Robert Fledrich and 4 more

Open access · goldAbstract read
In one paragraph

Article in eLife, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed
7.0field-weighted citation impact, top 2% 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

55 citing papers in PubMed, 94 citations in OpenAlex.

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  14. Schwann Cell Development and Myelination.Cold Spring Harbor perspectives in biology · 2024
    Review
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  18. HomozygousGenes · 2024
    Article
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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

14 authors at 4 institutions in 2 countries.

Sophie B Siems *Department of Neurogenetics, Max Planck Institute of Experimental Medicine, Göttingen, Germany.
Olaf Jahn *Proteomics Group, Max Planck Institute of Experimental Medicine, Göttingen, Germany.ORCID 0000-0002-3397-8924
Maria A EichelDepartment of Neurogenetics, Max Planck Institute of Experimental Medicine, Göttingen, Germany.
Nirmal KannaiyanDepartment of Psychiatry and Psychotherapy, University Hospital, LMU Munich, Munich, Germany.
Lai Man N WuCentre for Discovery Brain Sciences, University of Edinburgh, Edinburgh, United Kingdom.
Diane L ShermanCentre for Discovery Brain Sciences, University of Edinburgh, Edinburgh, United Kingdom.
Kathrin KuschDepartment of Neurogenetics, Max Planck Institute of Experimental Medicine, Göttingen, Germany.ORCID 0000-0002-5079-502X
Dörte HesseProteomics Group, Max Planck Institute of Experimental Medicine, Göttingen, Germany.
Ramona B JungDepartment of Neurogenetics, Max Planck Institute of Experimental Medicine, Göttingen, Germany.
Robert FledrichDepartment of Neurogenetics, Max Planck Institute of Experimental Medicine, Göttingen, Germany.
Michael W SeredaDepartment of Neurogenetics, Max Planck Institute of Experimental Medicine, Göttingen, Germany.
Moritz J RossnerDepartment of Psychiatry and Psychotherapy, University Hospital, LMU Munich, Munich, Germany.
Peter J BrophyCentre for Discovery Brain Sciences, University of Edinburgh, Edinburgh, United Kingdom.
Hauke B WernerDepartment of Neurogenetics, Max Planck Institute of Experimental Medicine, Göttingen, Germany.ORCID 0000-0002-7710-5738
Max Planck Institute of Experimental Medicine · DEUniversity of Edinburgh · GBLMU Klinikum · DEUniversitätsmedizin Göttingen · DE

Funding

Deutsche Forschungsgemeinschaft RO 4076/3-2Deutsche Forschungsgemeinschaft WE 2720/2-2Deutsche Forschungsgemeinschaft WE 2720/4-1Deutsche Forschungsgemeinschaft WE 2720/5-1Wellcome 0842424Wellcome Trust
6 · The paper itself

Abstract

Proteome and transcriptome analyses aim at comprehending the molecular profiles of the brain, its cell-types and subcellular compartments including myelin. Despite the relevance of the peripheral nervous system for normal sensory and motor capabilities, analogous approaches to peripheral nerves and peripheral myelin have fallen behind evolving technical standards. Here we assess the peripheral myelin proteome by gel-free, label-free mass-spectrometry for deep quantitative coverage. Integration with RNA-Sequencing-based developmental mRNA-abundance profiles and neuropathy disease genes illustrates the utility of this resource. Notably, the periaxin-deficient mouse model of the neuropathy Charcot-Marie-Tooth 4F displays a highly pathological myelin proteome profile, exemplified by the discovery of reduced levels of the monocarboxylate transporter MCT1/SLC16A1 as a novel facet of the neuropathology. This work provides the most comprehensive proteome resource thus far to approach development, function and pathology of peripheral myelin, and a straightforward, accurate and sensitive workflow to address myelin diversity in health and disease.

Indexed as

AnimalsDemyelinating DiseasesGene Expression RegulationGenotypeMembrane ProteinsMiceMitochondrial MyopathiesMyelin ProteinsMyelin SheathPeripheral NervesProteomeRetinitis PigmentosaTranscriptomeMembrane ProteinsMyelin ProteinsperiaxinProteomecharcot-marie-tooth (cmt) neuropathydemyelinationmousemyelin proteomeneuroscienceperipheral nervous systemschwann cell

Identifiers

PMID32130108
PMCPMC7056269
OpenAlexW3009926058

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.