DNA methylation is a critical cell-intrinsic determinant of astrocyte differentiation in the fetal brain

被引:444
作者
Takizawa, T
Nakashima, K [1 ]
Namihira, M
Ochiai, W
Uemura, A
Yanagisawa, M
Fujita, N
Nakao, M
机构
[1] Kumamoto Univ, Inst Mol Embryol & Genet, Dept Cell Fate Modulat, Kumamoto 8600811, Japan
[2] Kumamoto Univ, Sch Med, Dept Pediat, Kumamoto 8600811, Japan
[3] Kumamoto Univ, Sch Med, Dept Tumor Genet & Biol, Kumamoto 8600811, Japan
[4] Gunma Univ, Sch Med, Dept Pediat, Gunma 3718511, Japan
关键词
D O I
10.1016/S1534-5807(01)00101-0
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Astrocyte differentiation, which occurs late in brain development, is largely dependent on the activation of a transcription factor, STAT3. We show that astrocytes, as judged by glial fibrillary acidic protein (GFAP) expression, never emerge from neuroepithelial cells on embryonic day (E) 11.5 even when STAT3 is activated, in contrast to E14.5 neuroepithelial cells. A CpG dinucleotide within a STAT3 binding element in the GFAP promoter is highly methylated in E11.5 neuroepithelial cells, but is demethylated in cells responsive to the STAT3 activation signal to express GFAP. This CpG methylation leads to inaccessibility of STAT3 to the binding element. We suggest that methylation of a cell type-specific gene promoter is a pivotal event in regulating lineage specification in the developing brain.
引用
收藏
页码:749 / 758
页数:10
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