Evidence map›Paper›PMID 28808306›Full record

ArticleScientific reports2017

PHF20 positively regulates osteoblast differentiation via increasing the expression and activation of Runx2 with enrichment of H3K4me3.

Jin-Woo Yang, Byung-Chul Jeong, Jongsun Park, Jeong-Tae Koh

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. 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
0.9field-weighted citation impact, top 26% 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

11 citing papers in PubMed, 19 citations in OpenAlex.

  1. Review
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  8. Review
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  10. Wholemount In Situ Hybridization for Astyanax Embryos.Journal of visualized experiments : JoVE · 2019
    Article
  11. KLF2 regulates osteoblast differentiation by targeting of Runx2.Laboratory investigation; a journal of technical methods and pathology · 2019
    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

4 authors at 2 institutions in 1 country.

Jin-Woo YangDepartment of Pharmacology and Dental Therapeutics, School of Dentistry, Chonnam National University, Gwangju, 61186, South Korea.ORCID 0000-0001-8553-8261
Byung-Chul JeongDepartment of Pharmacology and Dental Therapeutics, School of Dentistry, Chonnam National University, Gwangju, 61186, South Korea.
Jongsun ParkDepartment of Pharmacology and Medical Science, College of Medicine, Chungnam National University, Daejeon, 35015, South Korea.ORCID 0000-0002-4690-1854
Jeong-Tae KohDepartment of Pharmacology and Dental Therapeutics, School of Dentistry, Chonnam National University, Gwangju, 61186, South Korea. jtkoh@chonnam.ac.kr.
Chonnam National University · KRChungnam National University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Plant homeodomain finger protein 20 (PHF20), a methyl lysine effector protein, is a component MOF-NSL lysine acetyltranferase complex. Global deletion of PHF20 has shown spinal bone defects and reduced skeletal formation. However, the molecular basis of PHF20 involved in skeletal development has not been elucidated yet. The objective of this study was to determine the role of PHF20 in osteoblast differentiation and mineralization. Expression of PHF20 was gradually increased during osteoblast differentiation. Overexpression of PHF20 enhanced ALP activity and mineralized nodule formation as well as the expression of osteogenic markers including Runx2. In contrast, inhibition of PHF20 expression reduced osteoblast differentiation and mineralization. Mechanistically, PHF20 increased the promoter activity of osteogenic genes including Og2, Alp, and Bsp through direct association with Runx2. Moreover, PHF20 increased the enrichment of H3K4me3 on the promoter of Runx2 followed by increased Runx2 promoter activity. Interestingly, Bix-01294, a histone methylation inhibitor, decreased mineralized nodule formation through decreasing the levels of H3K4me3 and Runx2. Overexpression of PHF20 restored the Bix-01294 effects. Taken together, these results indicate that methyl lysine-binding protein PHF20 might be a novel regulator of osteoblast differentiation.

Indexed as

AnimalsCell DifferentiationCells, CulturedCore Binding Factor Alpha 1 SubunitDNA-Binding ProteinsHEK293 CellsHistonesHomeodomain ProteinsHumansLysineMethylationMiceOsteoblastsOsteogenesisPromoter Regions, GeneticTranscription FactorsCore Binding Factor Alpha 1 SubunitDNA-Binding ProteinsHistonesHomeodomain ProteinsLysinePHF20 protein, mouseRunx2 protein, mouseTranscription Factors

Identifiers

PMID28808306
PMCPMC5556080
OpenAlexW2744829262

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.