Evidence map›Paper›PMID 22581805›Full record

ArticleGlycobiology2012

Detailed O-glycomics of the Muc2 mucin from colon of wild-type, core 1- and core 3-transferase-deficient mice highlights differences compared with human MUC2.

Kristina A Thomsson, Jessica M Holmén-Larsson, Jonas Angström, Malin Ev Johansson, Lijun Xia, Gunnar C Hansson

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in Glycobiology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 67 papers.

0numbers the graph read from it
0cells of the map it votes in
67citing papers in PubMed
3.2field-weighted citation impact, top 7% 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

67 citing papers in PubMed, 100 citations in OpenAlex.

  1. Article
  2. Article
  3. Degradation of mucinbioRxiv : the preprint server for biology · 2026
    Article
  4. Article
  5. Mucinase fromFrontiers in microbiology · 2026
    Article
  6. Article
  7. Review
  8. Review
  9. Article
  10. Article
  11. Article
  12. Frontiers in immunology · 2025
    Article
  13. Article
  14. O-glycosylation contributes to mammalian glycoRNA biogenesis.bioRxiv : the preprint server for biology · 2024
    Article
  15. Article
  16. Article
  17. Revealing Glycosylation Patterns inJournal of agricultural and food chemistry · 2024
    Article
  18. Article
  19. Article
  20. Review

7 more citing papers are in PubMed but not listed here.

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 2 countries.

Kristina A ThomssonDepartment of Medical Biochemistry, University of Gothenburg, PO Box 440, 405 30 Gothenburg, Sweden. kristina.thomsson@medkem.gu.se
Jessica M Holmén-Larsson
Jonas Angström
Malin Ev Johansson
Lijun Xia
Gunnar C Hansson
University of Gothenburg · SEOklahoma Medical Research Foundation · US

Funding

Role of Mucin-type O-glycans in Intestinal InflammationR01DK085691 · NIDDK · OKLAHOMA MEDICAL RESEARCH FOUNDATION · PI David Casero, Lijun Xia · 2010 to 2026
$6.2M
The MUC2 Mucus Gel as an Innate Immune Mechanism that Inhibits InflammationU01AI095473 · NIAID · GOTEBORG UNIVERSITY · PI HANSSON, GUNNAR C., JOHANSSON, MALIN E.V. · 2011 to 2020
$2.6M
NIAID NIH HHS U01 AI095473NIAID NIH HHS U01AI095473NIDDK NIH HHS R01 DK085691NIDDK NIH HHS R01DK085691
6 · The paper itself

Abstract

The heavily O-glycosylated mucin MUC2 constitutes the major protein in the mucosal layer that acts as a physical barrier protecting the epithelial layer in the colon. In this study, Muc2 was purified from mucosal scrapings from the colon of wild-type (WT) mice, core 3 transferase knockout (C3Gnt(-/-)) mice and intestinal epithelial cell-specific core 1 knockout (IEC C1Galt1(-/-)) mice. The Muc2 O-glycans were released by reductive β-elimination and analyzed with liquid chromatography-mass spectrometry in the negative-ion mode. Muc2 from the distal colon of WT and C3Gnt(-/-) knockout mice carried a mixture of core 1- or core 2-type glycans, whereas Muc2 from IEC C1Galt1(-/-) mice carried highly sialylated core 3- and core 4-type glycans. A large portion of NeuAc in all mouse models was positioned on disialylated N-acetyllactosamine units, an epitope not reported on human colonic MUC2. Mass spectra and proton NMR spectroscopy revealed an abundant NeuAc linked to internally positioned N-acetylglucosamine on colonic murine Muc2, which also differs markedly from human MUC2. Our results highlight that murine colonic Muc2 O-glycosylation is substantially different from human MUC2, which could be one explanation for the different commensal microbiota of these two species.

Indexed as

GlycomicsAmino SugarsAnimalsCarbohydrate SequenceChromatography, LiquidColonEpitopesGalactosyltransferasesGlycosylationHumansIntestinal MucosaMagnetic Resonance SpectroscopyMetagenomeMiceMice, Inbred C57BLMice, KnockoutAmino Sugarsbeta-1,3-galactosyl-O-glycosyl-glycoprotein beta-1,6-N-acetylglucosaminyltransferase 3C1galt1 protein, mouseEpitopesGalactosyltransferasesMUC2 protein, humanMuc2 protein, mouseMucin-2N-AcetylglucosaminyltransferasesN-acetyllactosaminePolysaccharides

Identifiers

PMID22581805
PMCPMC3382349
OpenAlexW2161300555

What OpenQuestion holds

Textmetadata
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.