Ezh2‐dependent H3K27me3 modification dynamically regulates vitamin D3‐dependent epigenetic control of CYP24A1 gene expression in osteoblastic cells-Reference-Cited by-同舟云学术

Ezh2‐dependent H3K27me3 modification dynamically regulates vitamin D3‐dependent epigenetic control of CYP24A1 gene expression in osteoblastic cells

Published:2020-01-07 Issue:6 Volume:235 Page:5404-5412
ISSN:0021-9541
Container-title:Journal of Cellular Physiology
language:en
Short-container-title:J Cell Physiol

Author:

Moena Daniel¹²,Nardocci Gino¹,Acevedo Elvis¹,Lian Jane³,Stein Gary³,Stein Janet³^ORCID,Montecino Martin¹^ORCID

Affiliation:

1. Institute of Biomedical Sciences and FONDAP Center for Genome Regulation, Faculty of Medicine and Faculty of Life SciencesUniversidad Andres Bello Santiago Chile

2. Department of Biological Sciences, Faculty of Life SciencesUniversidad Andres Bello Concepcion Chile

3. Department of BiochemistryUniversity of Vermont College of Medicine Burlington Vermont

Funder

National Institutes of Health

Fondo Nacional de Desarrollo Científico y Tecnológico

Publisher

Wiley

Subject

Cell Biology,Clinical Biochemistry,Physiology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/jcp.29428

Reference43 articles.

1. The emerging functions of histone demethylases

2. Recruitment and subnuclear distribution of the regulatory machinery during 1α,25-dihydroxy vitamin D3-mediated transcriptional upregulation in osteoblasts

4. The 1α,25-dihydroxy Vitamin D3 receptor preferentially recruits the coactivator SRC-1 during up-regulation of the osteocalcin gene

5. 1α,25-dihydroxy vitamin D3-enhanced expression of the osteocalcin gene involves increased promoter occupancy of basal transcription regulators and gradual recruitment of the 1α,25-dihydroxy vitamin D3 receptor-SRC-1 coactivator complex

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