Fan Guoping, Martinowich Keri, Chin Mark H, He Fei, Fouse Shaun D, Hutnick Leah, Hattori Daisuke, Ge Weihong, Shen Yin, Wu Hao, ten Hoeve Johanna, Shuai Ke, Sun Yi E
Department of Human Genetics, University of California at Los Angeles, 695 Charles Young Drive South, Los Angeles, CA 90095, USA.
Development. 2005 Aug;132(15):3345-56. doi: 10.1242/dev.01912.
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.
DNA甲基化是一种主要的表观遗传因子,据推测可调节细胞谱系分化。我们在此报告,在神经祖细胞(NPCs)中条件性基因缺失维持性DNA甲基转移酶I(Dnmt1)会导致DNA低甲基化和过早的星形胶质细胞分化。在Dnmt1基因敲除的NPCs中,星形胶质细胞标记基因以及编码胶质生成JAK-STAT途径关键成分的基因的发育调控去甲基化加速。通过染色质重塑过程,JAK-STAT途径中基因的去甲基化导致STATs的激活增强,进而触发星形胶质细胞分化。我们的研究表明,在神经发生期,DNA甲基化不仅抑制星形胶质细胞标记基因,还抑制JAK-STAT信号传导所必需的基因。因此,这两组基因的去甲基化以及随后STAT活性的升高是控制星形胶质细胞分化的时间和程度的关键机制。