Namihira Masakazu, Kohyama Jun, Abematsu Masahiko, Nakashima Kinichi
Graduate School of Biological Sciences, Nara Institute of Science and Technology, 8916-5 Takayama-cho, Ikoma 630-0101, Japan.
Philos Trans R Soc Lond B Biol Sci. 2008 Jun 27;363(1500):2099-109. doi: 10.1098/rstb.2008.2262.
Neural stem cells (NSCs) possess the ability to self-renew and to differentiate along neuronal and glial lineages. These processes are defined by the dynamic interplay between extracellular cues including cytokine signalling and intracellular programmes such as epigenetic modification. There is increasing evidence that epigenetic mechanisms involving, for example, changes in DNA methylation, histone modification and non-coding RNA expression are closely associated with fate specification of NSCs. These epigenetic alterations could provide coordinated systems for regulating gene expression at each step of neural cell differentiation. Here we review the roles of epigenetics in neural fate specification in the mammalian central nervous system.
神经干细胞(NSCs)具有自我更新以及沿神经元和神经胶质谱系分化的能力。这些过程由细胞外信号(包括细胞因子信号传导)和细胞内程序(如表观遗传修饰)之间的动态相互作用所定义。越来越多的证据表明,涉及DNA甲基化、组蛋白修饰和非编码RNA表达变化等的表观遗传机制与神经干细胞的命运决定密切相关。这些表观遗传改变可为神经细胞分化各阶段的基因表达调控提供协调系统。在此,我们综述表观遗传学在哺乳动物中枢神经系统神经命运决定中的作用。