Literature DB >> 16631596

The orphan nuclear receptor GCNF recruits DNA methyltransferase for Oct-3/4 silencing.

Noriko Sato1, Mitsumasa Kondo, Ken-ichi Arai.   

Abstract

Somatic DNA methylation patterns are determined in part by the de novo methylation that occurs after early embryonic demethylation. Oct-3/4, a pluripotency gene, is unmethylated in the blastocyst, but undergoes de novo methylation and silencing during gastrulation. Here we show that the transcriptional repressor GCNF recruits DNA methyltransferase to the Oct-3/4 promoter and facilitates its methylation. Although acetylation of histone H3 at lysine 9 (K9) and/or 14 (K14) and methylation of H3 at lysine 4 (K4) decrease during this period, as do Oct-3/4 transcript levels, H3K9 and H3K27 methylation levels remain constant, indicating that DNA methylation does not require repressive histone modifications. We found that GCNF interacts directly with Dnmt3 molecule(s) and verified that this interaction induces the methylation of the Oct-3/4 promoter. Our finding suggests a model in which differentiation-induced GCNF recruits de novo DNA methyltransferase and facilitates the silencing of a pluripotency gene.

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Year:  2006        PMID: 16631596     DOI: 10.1016/j.bbrc.2006.04.007

Source DB:  PubMed          Journal:  Biochem Biophys Res Commun        ISSN: 0006-291X            Impact factor:   3.575


  33 in total

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Journal:  Nat Genet       Date:  2011-10-02       Impact factor: 38.330

Review 2.  Cross-talk between site-specific transcription factors and DNA methylation states.

Authors:  Adam Blattler; Peggy J Farnham
Journal:  J Biol Chem       Date:  2013-10-22       Impact factor: 5.157

Review 3.  Minireview: the diverse roles of nuclear receptors in the regulation of embryonic stem cell pluripotency.

Authors:  Ryan T Wagner; Austin J Cooney
Journal:  Mol Endocrinol       Date:  2013-03-15

4.  Multiple genes exhibit phenobarbital-induced constitutive active/androstane receptor-mediated DNA methylation changes during liver tumorigenesis and in liver tumors.

Authors:  Jennifer M Phillips; Jay I Goodman
Journal:  Toxicol Sci       Date:  2009-02-20       Impact factor: 4.849

5.  Tissue specific differentially methylated regions (TDMR): Changes in DNA methylation during development.

Authors:  Fei Song; Saleh Mahmood; Srimoyee Ghosh; Ping Liang; Domminic J Smiraglia; Hiroki Nagase; William A Held
Journal:  Genomics       Date:  2008-11-13       Impact factor: 5.736

6.  Epigenetic reprogramming of the germ cell nuclear factor gene is required for proper differentiation of induced pluripotent cells.

Authors:  Hongran Wang; Xiaohong Wang; Xueping Xu; Thomas P Zwaka; Austin J Cooney
Journal:  Stem Cells       Date:  2013-12       Impact factor: 6.277

Review 7.  Transcriptional regulation of the Oct4 gene, a master gene for pluripotency.

Authors:  Steven Kellner; Nobuaki Kikyo
Journal:  Histol Histopathol       Date:  2010-03       Impact factor: 2.303

8.  Targeting of de novo DNA methylation throughout the Oct-4 gene regulatory region in differentiating embryonic stem cells.

Authors:  Rodoniki Athanasiadou; Dina de Sousa; Kevin Myant; Cara Merusi; Irina Stancheva; Adrian Bird
Journal:  PLoS One       Date:  2010-04-01       Impact factor: 3.240

9.  GCNF-dependent activation of cyclin D1 expression via repression of Mir302a during ESC differentiation.

Authors:  Hongran Wang; Xiaohong Wang; Trevor K Archer; Thomas P Zwaka; Austin J Cooney
Journal:  Stem Cells       Date:  2014-06       Impact factor: 6.277

10.  Functional cooperation between CREM and GCNF directs gene expression in haploid male germ cells.

Authors:  Mirjana Rajkovic; K Alexander H Iwen; Peter J Hofmann; Angelika Harneit; Joachim M Weitzel
Journal:  Nucleic Acids Res       Date:  2010-01-13       Impact factor: 16.971

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