Evidence map›Paper›PMID 40004117›Full record

ArticleInternational journal of molecular sciences2025

An Osteoblast-Specific Enhancer and Subenhancer Cooperatively Regulate

Yuki Matsuo, Xin Qin, Takeshi Moriishi, Viviane K S Kawata-Matsuura, Hisato Komori, Chiharu Sakane, Suemi Yabuta, Qing Jiang, Hitomi Kaneko, Kosei Ito and 3 more

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
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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.

Yuki MatsuoDepartment of Molecular Tumor Biology, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki 852-8588, Japan.
Xin QinDepartment of Molecular Tumor Biology, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki 852-8588, Japan.
Takeshi MoriishiDepartment of Skeletal Development and Regenerative Biology, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki 852-8588, Japan.
Viviane K S Kawata-MatsuuraDepartment of Molecular Tumor Biology, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki 852-8588, Japan.
Hisato KomoriDepartment of Molecular Tumor Biology, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki 852-8588, Japan.
Chiharu SakaneResearch Center for Biomedical Models and Animal Welfare, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki 852-8588, Japan.ORCID 0000-0002-6895-0577
Suemi YabutaDepartment of Molecular Tumor Biology, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki 852-8588, Japan.
Qing JiangDepartment of Molecular Tumor Biology, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki 852-8588, Japan.ORCID 0000-0003-1875-6263
Hitomi KanekoDepartment of Molecular Tumor Biology, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki 852-8588, Japan.
Kosei ItoDepartment of Molecular Tumor Biology, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki 852-8588, Japan.ORCID 0000-0002-8416-2466
Mayo ShigetaLaboratory for Animal Resources and Genetic Engineering, RIKEN Center for Biosystems Dynamics Research, Kobe 650-0047, Japan.
Takaya AbeLaboratory for Animal Resources and Genetic Engineering, RIKEN Center for Biosystems Dynamics Research, Kobe 650-0047, Japan.ORCID 0000-0001-5885-4875
Toshihisa KomoriDepartment of Molecular Tumor Biology, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki 852-8588, Japan.

Funding

Japan Society for the Promotion of Science 22K11805Japan Society for the Promotion of Science 23H00440Japan Society for the Promotion of Science 23K08591Japan Society for the Promotion of Science 23K09120Japan Society for the Promotion of Science 23K09121Japan Society for the Promotion of Science 24K12356Japan Society for the Promotion of Science 24K19001Natural Science Foundation of Jiangsu Province SL24700224
6 · The paper itself

Abstract

Runx2 is an essential transcription factor for osteoblast differentiation and chondrocyte maturation. The spatiotemporal expression of Runx2 is regulated by enhancers. We previously identified a 1.3 kb osteoblast-specific enhancer; however, mice with this deletion showed no phenotypes. A 0.8 kb conserved region detected near the 1.3 kb enhancer did not exhibit enhancer activity in reporter assays, whereas four tandem repeats of 452 bp (452 × 4) containing the most conserved region of 0.8 kb induced strong reporter activity in chondrocyte cell lines. However, chondrocytes of enhanced green fluorescent protein (EGFP) reporter mice using 452 × 4 did not express EGFP. When 452 × 4 was combined with the 1.3 kb enhancer, hypertrophic chondrocytes highly expressed EGFP. Moreover, the 0.8 kb region combined with the 1.3 kb enhancer induced EGFP expression in prehypertrophic and hypertrophic chondrocytes. The deletion of both the 1.3 kb enhancer and the 0.8 kb conserved region slightly reduced Runx2 expression in the limbs. However, neither homozygous nor heterozygous deletions in the Runx2

Indexed as

ChondrocytesCore Binding Factor Alpha 1 SubunitEnhancer Elements, GeneticGene Expression RegulationOsteoblastsAnimalsCell DifferentiationCell LineGreen Fluorescent ProteinsMiceCore Binding Factor Alpha 1 Subunitenhanced green fluorescent proteinGreen Fluorescent ProteinsRunx2 protein, mousechondrocyteenhancerosteoblastRunx2transcriptional regulation

Identifiers

PMID40004117
PMCPMC11855347

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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.