Bivalent histone modifications during tooth development.

Li-wei Zheng; Bin-peng Zhang; Ruo-shi XU; Xin XU; Ling YE; Xue-dong Zhou

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Bivalent histone modifications during tooth development.

Author: Li-Wei ZHENG ¹ ; Bin-Peng ZHANG ² ; Ruo-Shi XU ² ; Xin XU ² ; Ling YE ² ; Xue-Dong ZHOU ²
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1. 1] State Key Laboratory of Oral Diseases, West China Hospital of Stomatology, Sichuan University, Chengdu, China [2] Department of Orthopedics, Johns Hopkins University, Baltimore, USA.
2. 1] State Key Laboratory of Oral Diseases, West China Hospital of Stomatology, Sichuan University, Chengdu, China [2] West China School of Stomatology, Sichuan University, Chengdu, China.
Publication Type:Journal Article
MeSH: Animals; Cell Differentiation; physiology; DNA-Binding Proteins; analysis; Dental Papilla; embryology; Embryo, Mammalian; Enamel Organ; embryology; Enhancer of Zeste Homolog 2 Protein; Epigenesis, Genetic; physiology; Gene Expression Regulation, Developmental; Histone-Lysine N-Methyltransferase; analysis; Histones; metabolism; Jumonji Domain-Containing Histone Demethylases; analysis; Lysine; metabolism; Methylation; Mice; Mice, Inbred BALB C; Odontogenesis; physiology; Polycomb Repressive Complex 2; analysis; Protein Processing, Post-Translational; physiology; Tooth Germ; embryology
From: International Journal of Oral Science 2014;6(4):205-211
CountryChina
Language:English
Abstract: Histone methylation is one of the most widely studied post-transcriptional modifications. It is thought to be an important epigenetic event that is closely associated with cell fate determination and differentiation. To explore the spatiotemporal expression of histone H3 lysine 4 trimethylation (H3K4me3) and histone H3 lysine 27 trimethylation (H3K27me3) epigenetic marks and methylation or demethylation transferases in tooth organ development, we measured the expression of SET7, EZH2, KDM5B and JMJD3 via immunohistochemistry and quantitative polymerase chain reaction (qPCR) analysis in the first molar of BALB/c mice embryos at E13.5, E15.5, E17.5, P0 and P3, respectively. We also measured the expression of H3K4me3 and H3K27me3 with immunofluorescence staining. During murine tooth germ development, methylation or demethylation transferases were expressed in a spatial-temporal manner. The bivalent modification characterized by H3K4me3 and H3K27me3 can be found during the tooth germ development, as shown by immunofluorescence. The expression of SET7, EZH2 as methylation transferases and KDM5B and JMJD3 as demethylation transferases indicated accordingly with the expression of H3K4me3 and H3K27me3 respectively to some extent. The bivalent histone may play a critical role in tooth organ development via the regulation of cell differentiation.