DNA methylation controls the timing of astrogliogenesis through regulation of JAK-STAT signaling

被引:306
作者
Fan, GP
Martinowich, K
Chin, MH
He, F
Fouse, SD
Hutnick, L
Hattori, D
Ge, WH
Shen, Y
Hao, W
ten Hoeve, J
Shuai, K
Sun, YE
机构
[1] Univ Calif Los Angeles, Dept Human Genet, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, MRRC, Los Angeles, CA 90095 USA
[3] Univ Calif Los Angeles, Dept Mol & Med Pharmcol, Los Angeles, CA 90095 USA
[4] Univ Calif Los Angeles, Dept Psychiat & Behav Sci, Los Angeles, CA 90095 USA
[5] Univ Calif Los Angeles, Neuropsychiat Inst, Los Angeles, CA 90095 USA
[6] Univ Calif Los Angeles, Dept Biol Chem, Los Angeles, CA 90095 USA
[7] Univ Calif Los Angeles, Dept Med, Los Angeles, CA 90095 USA
来源
DEVELOPMENT | 2005年 / 132卷 / 15期
关键词
Dnmt1; CpG methylation; neural differentiation; STAT1; chromatin remodeling; MeCP2; histone modification; mouse;
D O I
10.1242/dev.01912
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
DNA methylation is a major epigenetic factor that has been postulated to regulate cell lineage differentiation. We report here that conditional gene deletion of the maintenance DNA methyltransferase I (Dnmt1) in neural progenitor cells (NPCs) results in DNA hypomethylation and precocious astroglial differentiation. The developmentally regulated demethylation of astrocyte marker genes as well as genes encoding the crucial components of the gliogenic JAK-STAT pathway is accelerated in Dnmt1(-/-) NPCs. Through a chromatin remodeling process, demethylation of genes in the JAK-STAT pathway leads to an enhanced activation of STATs, which in turn triggers astrocyte differentiation. Our study suggests that during the neurogenic period, DNA methylation inhibits not only astroglial marker genes but also genes that are essential for JAK-STAT signaling. Thus, demethylation of these two groups of genes and subsequent elevation of STAT activity are key mechanisms that control the timing and magnitude of astroglial differentiation.
引用
收藏
页码:3345 / 3356
页数:12
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