Evidence map›Paper›PMID 23300083›Full record

ArticleThe Journal of biological chemistry2013

Runx2 protein represses Axin2 expression in osteoblasts and is required for craniosynostosis in Axin2-deficient mice.

Meghan E McGee-Lawrence, Xiaodong Li, Krista L Bledsoe, Hai Wu, John R Hawse, Malayannan Subramaniam, David F Razidlo, Bridget A Stensgard, Gary S Stein, Andre J van Wijnen and 3 more

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed, 1 pooled it
2.5field-weighted citation impact, top 10% 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

26 citing papers in PubMed, 1 synthesis or guideline pooled it, 36 citations in OpenAlex.

  1. Pooled it
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  12. Integrative regulation of physiology by histone deacetylase 3.Nature reviews. Molecular cell biology · 2019
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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

13 authors at 3 institutions in 1 country.

Meghan E McGee-LawrenceMayo Clinic, Rochester, Minnesota 55905, USA.
Xiaodong Li
Krista L Bledsoe
Hai Wu
John R Hawse
Malayannan Subramaniam
David F Razidlo
Bridget A Stensgard
Gary S Stein
Andre J van Wijnen
Jane B Lian
Wei Hsu
Jennifer J Westendorf
Mayo Clinic · USUniversity of Vermont · USUniversity of Rochester Medical Center · US

Funding

GENETIC REGULATORY NETWORK IN CRANIOFACIAL DEVELOPMENTR01DE015654 · NIDCR · UNIVERSITY OF ROCHESTER · PI Wei Hsu · 2006 to 2026
$8.2M
CONTROL OF OSTEOBLAST PROLIFERATION AND DIFFERENTIATIONR01AR039588 · NIAMS · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI LIAN, JANE B., STEIN, GARY S. · 1990 to 2019
$8.0M
Musculoskeletal Research Training ProgramT32AR056950 · NIAMS · MAYO CLINIC ROCHESTER · PI Jennifer J Westendorf · 2009 to 2026
$7.0M
Molecular Control of Bone FormationR01AR049069 · NIAMS · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI WESTENDORF, JENNIFER J · 2003 to 2021
$5.8M
Synthesis of Osteocalcin in BoneR37DE012528 · NIDCR · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI LIAN, JANE B. · 2008 to 2017
$5.0M
REGULATION OF RUNX-2 TRANSCRIPTIONAL ACTIVITYR01AR048147 · NIAMS · UNIVERSITY OF MINNESOTA TWIN CITIES · PI WESTENDORF, JENNIFER J · 2002 to 2010
$2.7M
Runx2 and Axin2 Interactions During Bone FormationR01DE020194 · NIDCR · MAYO CLINIC ROCHESTER · PI WESTENDORF, JENNIFER J · 2010 to 2014
$2.1M
Tumor Microenvironment/Angiogenesis Training GrantT32CA148073 · NCI · MAYO CLINIC ROCHESTER · PI MC NIVEN, MARK A. · 2010 to 2014
$1.2M
Relationship between Hdac3 suppression and Wnt signaling in osteoblastsF32AR060140 · NIAMS · MAYO CLINIC ROCHESTER · PI MCGEE-LAWRENCE, MEGHAN E. · 2010 to 2011
$99k
NCI NIH HHS T32 CA148073NIAMS NIH HHS F32 AR060140NIAMS NIH HHS F32 AR60140NIAMS NIH HHS R01 AR039588NIAMS NIH HHS R01 AR048147NIAMS NIH HHS R01 AR049069NIAMS NIH HHS R01 AR48147NIAMS NIH HHS T32 AR056950NIDCR NIH HHS R01 DE015654NIDCR NIH HHS R01 DE020194NIDCR NIH HHS R37 DE012528
6 · The paper itself

Abstract

Runx2 and Axin2 regulate craniofacial development and skeletal maintenance. Runx2 is essential for calvarial bone development, as Runx2 haploinsufficiency causes cleidocranial dysplasia. In contrast, Axin2-deficient mice develop craniosynostosis because of high β-catenin activity. Axin2 levels are elevated in Runx2(-/-) calvarial cells, and Runx2 represses transcription of Axin2 mRNA, suggesting a direct relationship between these factors in vivo. Here we demonstrate that Runx2 binds several regions of the Axin2 promoter and that Runx2-mediated repression of Axin2 transcription depends on Hdac3. To determine whether Runx2 contributes to the etiology of Axin2 deficiency-induced craniosynostosis, we generated Axin2(-/-):Runx2(+/-) mice. These double mutant mice had longer skulls than Axin2(-/-) mice, indicating that Runx2 haploinsufficiency rescued the craniosynostosis phenotype of Axin2(-/-) mice. Together, these studies identify a key mechanistic pathway for regulating intramembranous bone development within the skull that involves Runx2- and Hdac3-mediated suppression of Axin2 to prevent the untimely closure of the calvarial sutures.

Indexed as

Gene Expression Regulation3T3 CellsAnimalsAxin ProteinBone and BonesBone Marrow CellsCore Binding Factor Alpha 1 SubunitCraniosynostosesGene ExpressionHistone Deacetylase 3Histone DeacetylasesMiceMice, KnockoutModels, BiologicalOsteoblastsPromoter Regions, GeneticAxin2 protein, mouseAxin ProteinCore Binding Factor Alpha 1 SubunitHistone Deacetylase 3Histone DeacetylasesRunx2 protein, mouseWnt Proteins

Identifiers

PMID23300083
PMCPMC3581413
OpenAlexW2063752728

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.