Department of Genetics and Developmental Biology, University of Connecticut Health Center, University of Connecticut Stem Cell Institute, Farmington, CT, USA.
Epigenetics. 2012 Jan 1;7(1):71-82. doi: 10.4161/epi.7.1.18750.
The de novo DNA methyltransferase DNMT3B functions in establishing DNA methylation patterns during development. DNMT3B missense mutations cause immunodeficiency, centromere instability and facial anomalies (ICF) syndrome. The restriction of Dnmt3b expression to neural progenitor cells, as well as the mild cognitive defects observed in ICF patients, suggests that DNMT3B may play an important role in early neurogenesis. We performed RNAi knockdown of DNMT3B in human embryonic stem cells (hESCs) in order to investigate the mechanistic contribution of DNMT3B to DNA methylation and early neuronal differentiation. While DNMT3B was not required for early neuroepithelium specification, DNMT3B deficient neuroepithelium exhibited accelerated maturation with earlier expression, relative to normal hESCs, of mature neuronal markers (such as NEUROD1) and of early neuronal regional specifiers (such as those for the neural crest). Genome-wide analyses of DNA methylation by MethylC-seq identified novel regions of hypomethylation in the DNMT3B knockdowns along the X chromosome as well as pericentromeric regions, rather than changes to promoters of specific dysregulated genes. We observed a loss of H3K27me3 and the polycomb complex protein EZH2 at the promoters of early neural and neural crest specifier genes during differentiation of DNMT3B knockdown but not normal hESCs. Our results indicate that DNMT3B mediates large-scale methylation patterns in hESCs and that DNMT3B deficiency in the cells alters the timing of their neuronal differentiation and maturation.
从头(de novo)DNA 甲基转移酶 DNMT3B 在发育过程中发挥作用,建立 DNA 甲基化模式。DNMT3B 错义突变导致免疫缺陷、着丝粒不稳定和面异常(ICF)综合征。Dnmt3b 表达限制在神经祖细胞中,以及在 ICF 患者中观察到的轻度认知缺陷,表明 DNMT3B 可能在早期神经发生中发挥重要作用。我们在人胚胎干细胞(hESCs)中进行了 DNMT3B 的 RNAi 敲低,以研究 DNMT3B 对 DNA 甲基化和早期神经元分化的机制贡献。虽然 DNMT3B 对于早期神经上皮的特化不是必需的,但 DNMT3B 缺陷的神经上皮表现出加速成熟,与正常 hESCs 相比,成熟神经元标志物(如 NEUROD1)和早期神经元区域特化标志物(如神经嵴标志物)的表达更早。通过 MethylC-seq 进行的全基因组 DNA 甲基化分析,在 DNMT3B 敲低的 X 染色体以及着丝粒周围区域发现了新的低甲基化区域,而不是特定失调基因的启动子发生变化。我们观察到在 DNMT3B 敲低的细胞分化过程中,早期神经和神经嵴特化基因的启动子处的 H3K27me3 和多梳复合物蛋白 EZH2 丢失,但在正常 hESCs 中则没有。我们的结果表明,DNMT3B 在 hESCs 中介导大规模的甲基化模式,而细胞中的 DNMT3B 缺乏会改变其神经元分化和成熟的时间。