Enam expression is regulated by Msx2

Author:

Ruspita Intan12,Das Pragnya13,Miyoshi Keiko4,Noma Takafumi5,Snead Malcolm L.6,Bei Marianna789ORCID

Affiliation:

1. Center for Regenerative and Developmental Biology The Forsyth Institute Cambridge Massachusetts USA

2. Department of Prosthodontics Universitas Gadjah Mada Yogyakarta Indonesia

3. Division of Neonatology Cooper University Hospital Camden New Jersey USA

4. Department of Molecular Biology, Institute of Biomedical Sciences Tokushima University Tokushima Japan

5. Faculty of Human Life Studies Hiroshima Jogakuin University Hiroshima Japan

6. Center for Craniofacial Molecular Biology, Herman Ostrow School of Dentistry of USC University of Southern California Los Angeles California USA

7. Department of Surgery, Center for Engineering in Medicine and Surgery Massachusetts General Hospital Boston Massachusetts USA

8. Department of Surgery Harvard Medical School Boston Massachusetts USA

9. Shriners Hospital for Children Boston Massachusetts USA

Abstract

AbstractBackgroundThe precise formation of mineralized dental tissues such as enamel and/or dentin require tight transcriptional control of the secretion of matrix proteins. Here, we have investigated the transcriptional regulation of the second most prominent enamel matrix protein, enamelin, and its regulation through the major odontogenic transcription factor, MSX2.ResultsUsing in vitro and in vivo approaches, we identified that (a) Enam expression is reduced in the Msx2 mouse mutant pre‐secretory and secretory ameloblasts, (b) Enam is an early response gene whose expression is under the control of Msx2, (c) Msx2 binds to Enam promoter in vitro, suggesting that enam is a direct target for Msx2 and that (d) Msx2 alone represses Enam gene expression.ConclusionsCollectively, these results illustrate that Enam gene expression is controlled by Msx2 in a spatio‐temporal manner. They also suggest that Msx2 may interact with other transcription factors to control spatial and temporal expression of Enam and hence amelogenesis and enamel biomineralization.

Funder

Massachusetts General Hospital

National Institute of Dental and Craniofacial Research

Publisher

Wiley

Subject

Developmental Biology

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