Evidence map›Paper›PMID 26801561›Full record

ArticleBiochemical and biophysical research communications2016

TIEG1 enhances Osterix expression and mediates its induction by TGFβ and BMP2 in osteoblasts.

Malayannan Subramaniam, Kevin S Pitel, Sarah G Withers, Hicham Drissi, John R Hawse

Open access · greenAbstract read
In one paragraph

Article in Biochemical and biophysical research communications, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.0field-weighted citation impact, top 22% 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

15 citing papers in PubMed, 33 citations in OpenAlex.

  1. Article
  2. Review
  3. Titanium Biohybrid Middle Ear Prostheses: A PreliminaryJournal of functional biomaterials · 2023
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  7. Kruppel-like Factors in Skeletal Physiology and Pathologies.International journal of molecular sciences · 2022
    Review
  8. Article
  9. Review
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. 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

5 authors at 3 institutions in 1 country.

Malayannan SubramaniamDepartment of Biochemistry and Molecular Biology, Mayo Clinic, Rochester, MN 55905, USA.
Kevin S PitelDepartment of Biochemistry and Molecular Biology, Mayo Clinic, Rochester, MN 55905, USA.
Sarah G WithersDepartment of Biochemistry and Molecular Biology, Mayo Clinic, Rochester, MN 55905, USA.
Hicham DrissiDepartment of Orthopaedic Surgery, UConn Musculoskeletal Institute, UConn Health, Farmington, CT 06030, USA.
John R HawseDepartment of Biochemistry and Molecular Biology, Mayo Clinic, Rochester, MN 55905, USA. Electronic address: hawse.john@mayo.edu.
Mayo Clinic · USUConn Health · USWinnMed · US

Funding

Role of a TGF-? Regulated Gene in Human and Mouse Osteoblasts and SkeletonR01DE014036 · NIDCR · MAYO CLINIC ROCHESTER · PI HAWSE, JOHN R., SUBRAMANIAM, MALAYANNAN · 2001 to 2016
$4.7M
Role of aTGF-beta Regulated Gene in human and mouse osteoblasts and skeletonR56DE014036 · NIDCR · MAYO CLINIC ROCHESTER · PI SPELSBERG, THOMAS C · 2007 to 2007
$352k
NIDCR NIH HHS DE14036NIDCR NIH HHS R01 DE014036NIDCR NIH HHS R56 DE014036
6 · The paper itself

Abstract

Deletion of TIEG1/KLF10 in mice results in an osteopenic skeletal phenotype with significant decreases in both bone mineral density and content throughout the skeleton. Calvarial osteoblasts isolated from TIEG1 knockout (KO) mice display numerous changes in gene expression and exhibit significant delays in their mineralization rates relative to wild-type (WT) controls. Here, we demonstrate that loss of TIEG1 expression in osteoblasts results in decreased levels of Osterix mRNA. Suppression of TIEG1 expression in WT osteoblasts leads to decreased Osterix expression while restoration of TIEG1 expression in TIEG1 KO osteoblasts results in increased levels of Osterix. Transient transfection and chromatin immunoprecipitation assays reveal that TIEG1 directly binds to and activates the Osterix promoter and demonstrate that the zinc finger-containing DNA binding domain of TIEG1 is necessary for this regulation. Furthermore, we reveal that TIEG1 expression is essential for the induction of Osterix expression by important bone-related cytokines such as TGFβ and BMP2 in osteoblast cells. Taken together, these data implicate an important role for TIEG1 in regulating the expression of Osterix, a master regulator of osteoblast differentiation and bone formation, and suggest that decreased expression of Osterix, as well as impaired TGFβ and BMP2 signaling, contribute to the observed osteopenic bone phenotype of TIEG1 KO mice.

Indexed as

AnimalsBone Diseases, MetabolicBone Morphogenetic Protein 2Cells, CulturedDNA-Binding ProteinsEarly Growth Response Transcription FactorsGene Expression RegulationKruppel-Like Transcription FactorsMiceMice, Inbred C57BLOsteoblastsSignal TransductionSp7 Transcription FactorTranscription FactorsTransforming Growth Factor betaBmp2 protein, mouseBone Morphogenetic Protein 2DNA-Binding ProteinsEarly Growth Response Transcription FactorsKLF10 protein, mouseKruppel-Like Transcription FactorsSp7 protein, mouseSp7 Transcription FactorTranscription FactorsTransforming Growth Factor betaBMP2KLF10OsteoblastOsterixTGFβTIEG1

Identifiers

PMID26801561
PMCPMC4747784
OpenAlexW2286186411

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Registered trials

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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.