Evidence map›Paper›PMID 36717059›Full record

ArticleMolecular & cellular proteomics : MCP2023

Increasing Complexity of the N-Glycome During Caenorhabditis Development.

Iain B H Wilson, Shi Yan, Chunsheng Jin, Zuzanna Dutkiewicz, Dubravko Rendić, Dieter Palmberger, Ralf Schnabel, Katharina Paschinger

Abstract read
In one paragraph

Article in Molecular & cellular proteomics : MCP, 2023. 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
–field-weighted citation impact
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.

  1. Article
  2. Article
  3. Article
  4. The Historiography of Galactose and Its Recognition by Galectins.Advances in experimental medicine and biology · 2026
    Review
  5. Article
  6. Dual roles ofFrontiers in immunology · 2025
    Article
  7. Analysis of Caenorhabditis Protein Glycosylation.Methods in molecular biology (Clifton, N.J.) · 2024
    Article
  8. Article
  9. Article
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

8 authors.

Iain B H WilsonDepartment für Chemie, Universität für Bodenkultur, Wien, Austria. Electronic address: iain.wilson@boku.ac.at.
Shi YanDepartment für Chemie, Universität für Bodenkultur, Wien, Austria; Institut für Parasitologie, Veterinärmedizinische Universität Wien, Wien, Austria.
Chunsheng JinInstitutionen för Biomedicin, Göteborgs universitet, Göteborg, Sweden.
Zuzanna DutkiewiczDepartment für Chemie, Universität für Bodenkultur, Wien, Austria.
Dubravko RendićDepartment für Chemie, Universität für Bodenkultur, Wien, Austria.
Dieter PalmbergerDepartment für Chemie, Universität für Bodenkultur, Wien, Austria.
Ralf SchnabelInstitut für Genetik, Technische Universität Braunschweig, Braunschweig, Germany.
Katharina PaschingerDepartment für Chemie, Universität für Bodenkultur, Wien, Austria.

Funding

Austrian Science Fund FWF P 23922Austrian Science Fund FWF P 29466Austrian Science Fund FWF P 30021Austrian Science Fund FWF P 32572Austrian Science Fund FWF TRP 127Austrian Science Fund FWF W 1224
6 · The paper itself

Abstract

Caenorhabditis elegans is a frequently employed genetic model organism and has been the object of a wide range of developmental, genetic, proteomic, and glycomic studies. Here, using an off-line MALDI-TOF-MS approach, we have analyzed the N-glycans of mixed embryos and liquid- or plate-grown L4 larvae. Of the over 200 different annotatable N-glycan structures, variations between the stages as well as the mode of cultivation were observed. While the embryonal N-glycome appears less complicated overall, the liquid- and plate-grown larvae differ especially in terms of methylation of bisecting fucose, α-galactosylation of mannose, and di-β-galactosylation of core α1,6-fucose. Furthermore, we analyzed the O-glycans by LC-electrospray ionization-MS following β-elimination; especially the embryonal O-glycomes included a set of phosphorylcholine-modified structures, previously not shown to exist in nematodes. However, the set of glycan structures cannot be clearly correlated with levels of glycosyltransferase transcripts in developmental RNA-Seq datasets, but there is an indication for coordinated expression of clusters of potential glycosylation-relevant genes. Thus, there are still questions to be answered in terms of how and why a simple nematode synthesizes such a diverse glycome.

Indexed as

CaenorhabditisAnimalsCaenorhabditis elegansChromatography, High Pressure LiquidFucoseGlycomicsPolysaccharidesProteomicsSpectrometry, Mass, Matrix-Assisted Laser Desorption-IonizationFucosePolysaccharidesfucosegalactoseglycomicsmass spectrometryphosphorylcholine

Identifiers

PMID36717059
PMCPMC7614267

What OpenQuestion holds

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LicenceCC BY
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.