Evidence map›Paper›PMID 22357927›Full record

ArticleDevelopment (Cambridge, England)2012

2-O-sulfotransferase regulates Wnt signaling, cell adhesion and cell cycle during zebrafish epiboly.

Erin L Cadwalader, Maureen L Condic, H Joseph Yost

Abstract read
In one paragraph

Article in Development (Cambridge, England), 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. Epithelial Heparan Sulfate PromotesProteoglycan research · 2025
    Article
  2. Adipocyte-specific deletion of HuR induces spontaneous cardiac hypertrophy and fibrosis.American journal of physiology. Heart and circulatory physiology · 2021
    Article
  3. Article
  4. Deciphering functional glycosaminoglycan motifs in development.Current opinion in structural biology · 2018
    Review
  5. Time-series analysis in imatinib-resistant chronic myeloid leukemia K562-cells under different drug treatments.Journal of Huazhong University of Science and Technology. Medical sciences = Hua zhong ke ji da xue xue bao. Yi xue Ying De wen ban = Huazhong keji daxue xuebao. Yixue Yingdewen ban · 2017
    Article
  6. Article
  7. Review
  8. Article
  9. Review
  10. Article
  11. 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

3 authors.

Erin L CadwaladerDepartment of Neurobiology and Anatomy, Eccles Institute of Human Genetics, University of Utah, Salt Lake City, UT 84112, USA.
Maureen L Condic
H Joseph Yost

Funding

Genetic regulation of left-right organ discordanceR01HL066292 · NHLBI · UNIVERSITY OF UTAH · PI YOST, H. JOSEPH · 2001 to 2009
$3.0M
Specification and development of sensory neuronsR01NS048382 · NINDS · UNIVERSITY OF UTAH · PI CONDIC, MAUREEN L · 2004 to 2009
$1.5M
NHLBI NIH HHS R01 HL066292NHLBI NIH HHS R01 HL66292NINDS NIH HHS R01 NS048382NINDS NIH HHS R01 NS48382
6 · The paper itself

Abstract

O-sulfotransferases modify heparan sulfate proteoglycans (HSPGs) by catalyzing the transfer of a sulfate to a specific position on heparan sulfate glycosaminoglycan (GAG) chains. Although the roles of specific HSPG modifications have been described in cell culture and invertebrates, little is known about their functions or abilities to modulate specific cell signaling pathways in vertebrate development. Here, we report that 2-O-sulfotransferase (2-OST) is an essential component of canonical Wnt signaling in zebrafish development. 2-OST-deficient embryos have reduced GAG chain sulfation and are refractory to exogenous Wnt8 overexpression. Embryos in which maternally encoded 2-OST is knocked down have normal activation of several zygotic mesoderm, endoderm and ectoderm patterning genes, but have decreased deep cell adhesion and fail to initiate epiboly, which can be rescued by re-expression of 2-OST protein. Reduced cell adhesion and altered cell cycle regulation in 2-OST-deficient embryos are associated with decreased β-catenin and E-cadherin protein levels at cell junctions, and these defects can be rescued by reactivation of the intracellular Wnt pathway, utilizing stabilized β-catenin or dominant-negative Gsk3, but not by overexpression of Wnt8 ligand. Together, these results indicate that 2-OST functions within the Wnt pathway, downstream of Wnt ligand signaling and upstream of Gsk3β and β-catenin intracellular localization and function.

Indexed as

AnimalsAnimals, Genetically Modifiedbeta CateninCadherinsCell AdhesionCell CycleCytoskeletal ProteinsGene Expression Regulation, DevelopmentalGlycogen Synthase Kinase 3Glycogen Synthase Kinase 3 betaHeparan Sulfate ProteoglycansLigandsModels, BiologicalSignal TransductionSulfotransferasesTranscription, Geneticbeta CateninCadherinsCytoskeletal ProteinsGlycogen Synthase Kinase 3Glycogen Synthase Kinase 3 betaGSK3B protein, humanheparan sulfate 2-O-sulfotransferase, zebrafishHeparan Sulfate ProteoglycansLigandsSulfotransferaseswnt8a protein, zebrafishWnt ProteinsZebrafish Proteins

Identifiers

PMID22357927
PMCPMC3294434

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.