DNA methylation changes during cleft palate formation induced by retinoic acid in mice

Motone Kuriyama, Akikazu Udagawa, Shinya Yoshimoto, Masaharu Ichinose, Koji Sato, Koji Yamazaki, Yoshiharu Matsuno, Kunio Shiota, Chisato Mori

Research output: Contribution to journalArticle

28 Citations (Scopus)

Abstract

Objectives: The aim of this study was to analyze epigenetic (specifically, DNA methylation) participation in the mechanisms of cleft palate only induced by maternal exposure to all-trans retinoic acid in mice. Design: Cleft palate only was induced in fetuses by maternal exposure to all-trans retinoic acid. Their secondary palates were excised for analysis. Cytosine extension assay and restriction landmark genomic scanning were performed to analyze DNA methylation status. The expression levels of the DNA methyl-transferases were examined by real-time reverse transcriptase-polymerase chain reaction. Results: Using cytosine extension assay, on gestation day 14.5, the status of DNA methylation within CpG islands and in global DNA was decreased significantly in all-trans retinoic acid-treated groups compared with the controls (p <.01 and p <.05). In the controls, the status within CpG islands on gestation day 14.5 was significantly increased compared with gestation days 13.5 and 18.5 (p <.01). Using real-time reverse transcriptase-polymerase chain reaction, there was no significant change in the expression of DNA methyltransferases, except on gestation day 18.5. Using restriction landmark genomic scanning on gestation day 18.5, five spots (0.49%) in the controls and one spot (0.1%) in all-trans retinoic acid-treated groups were specifically detected. Conclusions: These results indicate that changes in DNA methylation may play an important role in the manifestation of cleft palate only caused by environmental factors such as maternal exposure to all-trans retinoic acid.

Original languageEnglish
Pages (from-to)545-551
Number of pages7
JournalCleft Palate-Craniofacial Journal
Volume45
Issue number5
DOIs
Publication statusPublished - 2008 Sep
Externally publishedYes

Fingerprint

Cleft Palate
DNA Methylation
Tretinoin
Maternal Exposure
Pregnancy
CpG Islands
Cytosine
Reverse Transcriptase Polymerase Chain Reaction
Real-Time Polymerase Chain Reaction
DNA
Palate
Methyltransferases
Transferases
Epigenomics
Fetus

Keywords

  • Cleft palate
  • Cytosine extension assay
  • DNA methylation
  • DNA methyltransferase (Dnmt)
  • Epigenetics
  • Restriction landmark genomic scanning (RLGS)

ASJC Scopus subject areas

  • Otorhinolaryngology
  • Oral Surgery

Cite this

Kuriyama, M., Udagawa, A., Yoshimoto, S., Ichinose, M., Sato, K., Yamazaki, K., ... Mori, C. (2008). DNA methylation changes during cleft palate formation induced by retinoic acid in mice. Cleft Palate-Craniofacial Journal, 45(5), 545-551. https://doi.org/10.1597/07-134.1

DNA methylation changes during cleft palate formation induced by retinoic acid in mice. / Kuriyama, Motone; Udagawa, Akikazu; Yoshimoto, Shinya; Ichinose, Masaharu; Sato, Koji; Yamazaki, Koji; Matsuno, Yoshiharu; Shiota, Kunio; Mori, Chisato.

In: Cleft Palate-Craniofacial Journal, Vol. 45, No. 5, 09.2008, p. 545-551.

Research output: Contribution to journalArticle

Kuriyama, M, Udagawa, A, Yoshimoto, S, Ichinose, M, Sato, K, Yamazaki, K, Matsuno, Y, Shiota, K & Mori, C 2008, 'DNA methylation changes during cleft palate formation induced by retinoic acid in mice', Cleft Palate-Craniofacial Journal, vol. 45, no. 5, pp. 545-551. https://doi.org/10.1597/07-134.1
Kuriyama M, Udagawa A, Yoshimoto S, Ichinose M, Sato K, Yamazaki K et al. DNA methylation changes during cleft palate formation induced by retinoic acid in mice. Cleft Palate-Craniofacial Journal. 2008 Sep;45(5):545-551. https://doi.org/10.1597/07-134.1
Kuriyama, Motone ; Udagawa, Akikazu ; Yoshimoto, Shinya ; Ichinose, Masaharu ; Sato, Koji ; Yamazaki, Koji ; Matsuno, Yoshiharu ; Shiota, Kunio ; Mori, Chisato. / DNA methylation changes during cleft palate formation induced by retinoic acid in mice. In: Cleft Palate-Craniofacial Journal. 2008 ; Vol. 45, No. 5. pp. 545-551.
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abstract = "Objectives: The aim of this study was to analyze epigenetic (specifically, DNA methylation) participation in the mechanisms of cleft palate only induced by maternal exposure to all-trans retinoic acid in mice. Design: Cleft palate only was induced in fetuses by maternal exposure to all-trans retinoic acid. Their secondary palates were excised for analysis. Cytosine extension assay and restriction landmark genomic scanning were performed to analyze DNA methylation status. The expression levels of the DNA methyl-transferases were examined by real-time reverse transcriptase-polymerase chain reaction. Results: Using cytosine extension assay, on gestation day 14.5, the status of DNA methylation within CpG islands and in global DNA was decreased significantly in all-trans retinoic acid-treated groups compared with the controls (p <.01 and p <.05). In the controls, the status within CpG islands on gestation day 14.5 was significantly increased compared with gestation days 13.5 and 18.5 (p <.01). Using real-time reverse transcriptase-polymerase chain reaction, there was no significant change in the expression of DNA methyltransferases, except on gestation day 18.5. Using restriction landmark genomic scanning on gestation day 18.5, five spots (0.49{\%}) in the controls and one spot (0.1{\%}) in all-trans retinoic acid-treated groups were specifically detected. Conclusions: These results indicate that changes in DNA methylation may play an important role in the manifestation of cleft palate only caused by environmental factors such as maternal exposure to all-trans retinoic acid.",
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AU - Sato, Koji

AU - Yamazaki, Koji

AU - Matsuno, Yoshiharu

AU - Shiota, Kunio

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N2 - Objectives: The aim of this study was to analyze epigenetic (specifically, DNA methylation) participation in the mechanisms of cleft palate only induced by maternal exposure to all-trans retinoic acid in mice. Design: Cleft palate only was induced in fetuses by maternal exposure to all-trans retinoic acid. Their secondary palates were excised for analysis. Cytosine extension assay and restriction landmark genomic scanning were performed to analyze DNA methylation status. The expression levels of the DNA methyl-transferases were examined by real-time reverse transcriptase-polymerase chain reaction. Results: Using cytosine extension assay, on gestation day 14.5, the status of DNA methylation within CpG islands and in global DNA was decreased significantly in all-trans retinoic acid-treated groups compared with the controls (p <.01 and p <.05). In the controls, the status within CpG islands on gestation day 14.5 was significantly increased compared with gestation days 13.5 and 18.5 (p <.01). Using real-time reverse transcriptase-polymerase chain reaction, there was no significant change in the expression of DNA methyltransferases, except on gestation day 18.5. Using restriction landmark genomic scanning on gestation day 18.5, five spots (0.49%) in the controls and one spot (0.1%) in all-trans retinoic acid-treated groups were specifically detected. Conclusions: These results indicate that changes in DNA methylation may play an important role in the manifestation of cleft palate only caused by environmental factors such as maternal exposure to all-trans retinoic acid.

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