Evidence map›Paper›PMID 20727876›Full record

ArticleDevelopmental biology2010

Jagged1 functions downstream of Twist1 in the specification of the coronal suture and the formation of a boundary between osteogenic and non-osteogenic cells.

Hai-Yun Yen, Man-Chun Ting, Robert E Maxson

Open access · greenAbstract read
In one paragraph

Article in Developmental biology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

50 citing papers in PubMed, 74 citations in OpenAlex.

  1. Article
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  6. Complimentary vertebratebioRxiv : the preprint server for biology · 2025
    Article
  7. Review
  8. Non-syndromic craniosynostosis.Nature reviews. Disease primers · 2025
    Review
  9. Review
  10. Cranium growth, patterning and homeostasis.Development (Cambridge, England) · 2022
    Article
  11. Article
  12. Review
  13. Article
  14. Neuroradiological findings in Alagille syndrome.The British journal of radiology · 2022
    Review
  15. Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. Review
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 at 1 institution in 1 country.

Hai-Yun YenDepartment of Biochemistry and Molecular Biology, Norris Cancer Hospital, University of Southern California Keck School of Medicine, 1441 Eastlake Avenue, Los Angeles, CA 90089-9176, USA.
Man-Chun Ting
Robert E Maxson
University of Southern California · US

Funding

TWIST AND Msx2 IN BOUNDARY FORMATION AND CRANIOSYNOSTOSISR01DE016320 · NIDCR · UNIVERSITY OF SOUTHERN CALIFORNIA · PI MAXSON, ROBERT E. · 2005 to 2014
$3.9M
Cellular and Molecular Mechanisms of Patterned Growth of the Mammalian SkullR01DE019650 · NIDCR · UNIVERSITY OF SOUTHERN CALIFORNIA · PI MAXSON, ROBERT E. · 2009 to 2013
$1.9M
NIDCR NIH HHS DE16320NIDCR NIH HHS DE19650NIDCR NIH HHS R01 DE016320NIDCR NIH HHS R01 DE019650
6 · The paper itself

Abstract

The Notch pathway is crucial for a wide variety of developmental processes including the formation of tissue boundaries. That it may function in calvarial suture development and figure in the pathophysiology of craniosynostosis was suggested by the demonstration that heterozygous loss of function of JAGGED1 in humans can cause Alagille syndrome, which has craniosynostosis as a feature. We used conditional gene targeting to examine the role of Jagged1 in the development of the skull vault. We demonstrate that Jagged1 is expressed in a layer of mesoderm-derived sutural cells that lie along the osteogenic-non-osteogenic boundary. We show that inactivation of Jagged1 in the mesodermal compartment of the coronal suture, but not in the neural crest compartment, results in craniosynostosis. Mesodermal inactivation of Jagged1 also results in changes in the identity of sutural cells prior to overt osteogenic differentiation, as well as defects in the boundary between osteogenic and non-osteogenic compartments at the coronal suture. These changes, surprisingly, are associated with increased expression of Notch2 and the Notch effector, Hes1, in the sutural mesenchyme. They are also associated with an increase in nuclear β-catenin. In Twist1 mutants, Jagged1 expression in the suture is reduced substantially, suggesting an epistatic relationship between Twist1 and Jagged1. Consistent with such a relationship, Twist1-Jagged1 double heterozygotes exhibit a substantial increase in the severity of craniosynostosis over individual heterozygotes. Our results thus suggest that Jagged1 is an effector of Twist1 in coronal suture development.

Indexed as

AnimalsCalcium-Binding ProteinsCranial SuturesCraniosynostosesEpistasis, GeneticFemaleGene Expression Regulation, DevelopmentalHeterozygoteHumansIntercellular Signaling Peptides and ProteinsJagged-1 ProteinMembrane ProteinsMesodermMiceMice, KnockoutMice, Mutant StrainsCalcium-Binding ProteinsIntercellular Signaling Peptides and ProteinsJAG1 protein, humanJag1 protein, mouseJagged-1 ProteinMembrane ProteinsNuclear ProteinsSerrate-Jagged ProteinsTwist1 protein, mouseTwist-Related Protein 1

Identifiers

PMID20727876
PMCPMC3210079
OpenAlexW1968506415

What OpenQuestion holds

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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.