TY - JOUR
T1 - Developmental stage dependent regulation of DNA methylation and chromatin modification in a immature astrocyte specific gene promoter
AU - Namihira, Masakazu
AU - Nakashima, Kinichi
AU - Taga, Tetsuya
N1 - Funding Information:
We thank Yamanouchi Pharmaceutical Co. Ltd. for providing the human recombinant BMP2. We are very grateful to Ms. M. Ohta-Teramoto for her excellent secretarial assistance. We also thank Ms. K. Kaneko and Ms. Y. Saiki for technical help. This work was supported in part by grant-in-aid for 21st Century COE Research from Ministry of Education, Science and Culture `Cell Fate Regulation Research and Education Unit'; Scientific Research (B); Specially Promoted Research from the Ministry of Education, Culture, Science, Sports and Technology; Human Frontier Science Program; and the Virtual Research Institute of Aging of Nippon Boehringer Ingelheim.
PY - 2004/8/13
Y1 - 2004/8/13
N2 - Astrocytes are generated from neuroepithelial cells after neurons during brain development. However, the mechanism of this sequential generation is not fully understood. Here, we show that a particular cytosine residue in the promoter of the gene encoding the immature astrocyte marker, S100β, becomes demethylated, correlating with the time when the S100β expression commences at embryonic day (E) 14. In addition, astrocyte-inducing cytokine, BMP2, increased histone acetylation around the CpG site in neuroepithelial cells at E14 but not E11 when S100β expressing astrocytes are absent. Furthermore, binding of a methyl DNA binding protein, MeCP2, to the S100β gene promoter in neuroepithelial cells was reduced at E14 compared to E11. Thus, demethylation of specific CpG site is suggested to be a critical determinant in regulating astrocyte differentiation in the developing brain.
AB - Astrocytes are generated from neuroepithelial cells after neurons during brain development. However, the mechanism of this sequential generation is not fully understood. Here, we show that a particular cytosine residue in the promoter of the gene encoding the immature astrocyte marker, S100β, becomes demethylated, correlating with the time when the S100β expression commences at embryonic day (E) 14. In addition, astrocyte-inducing cytokine, BMP2, increased histone acetylation around the CpG site in neuroepithelial cells at E14 but not E11 when S100β expressing astrocytes are absent. Furthermore, binding of a methyl DNA binding protein, MeCP2, to the S100β gene promoter in neuroepithelial cells was reduced at E14 compared to E11. Thus, demethylation of specific CpG site is suggested to be a critical determinant in regulating astrocyte differentiation in the developing brain.
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U2 - 10.1016/j.febslet.2004.07.029
DO - 10.1016/j.febslet.2004.07.029
M3 - Article
C2 - 15304345
AN - SCOPUS:4143141064
SN - 0014-5793
VL - 572
SP - 184
EP - 188
JO - FEBS Letters
JF - FEBS Letters
IS - 1-3
ER -