表观遗传学
生物
人脑
DNA甲基化
类有机物
转录组
表观基因组
诱导多能干细胞
增强子
表观遗传学
神经科学
计算生物学
遗传学
细胞生物学
胚胎干细胞
基因表达
基因
作者
Chongyuan Luo,Madeline A. Lancaster,Rosa Castanon,Joseph R. Nery,Juergen A. Knoblich,Joseph R. Ecker
出处
期刊:Cell Reports
[Elsevier]
日期:2016-12-01
卷期号:17 (12): 3369-3384
被引量:325
标识
DOI:10.1016/j.celrep.2016.12.001
摘要
Organoids derived from human pluripotent stem cells recapitulate the early three-dimensional organization of the human brain, but whether they establish the epigenomic and transcriptional programs essential for brain development is unknown. We compared epigenomic and regulatory features in cerebral organoids and human fetal brain, using genome-wide, base resolution DNA methylome and transcriptome sequencing. Transcriptomic dynamics in organoids faithfully modeled gene expression trajectories in early-to-mid human fetal brains. We found that early non-CG methylation accumulation at super-enhancers in both fetal brain and organoids marks forthcoming transcriptional repression in the fully developed brain. Demethylated regions (74% of 35,627) identified during organoid differentiation overlapped with fetal brain regulatory elements. Interestingly, pericentromeric repeats showed widespread demethylation in multiple types of in vitro human neural differentiation models but not in fetal brain. Our study reveals that organoids recapitulate many epigenomic features of mid-fetal human brain and also identified novel non-CG methylation signatures of brain development.
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