DNA甲基化
表观遗传学
染色质
生物
电池类型
细胞
甲基化
DNA
基因
人脑
CpG站点
基因表达调控
计算生物学
基因组
人类基因组
遗传学
基因表达
神经科学
作者
Wei Tian,Jingtian Zhou,Anna Bartlett,Qiurui Zeng,Hanqing Liu,Rosa Castanon,Mia Kenworthy,Jordan Altshul,Cynthia Valadon,Andrew Aldridge,Joseph R. Nery,Huaming Chen,Jiaying Xu,Nicholas D. Johnson,Jacinta Lucero,Julia Osteen,Nora Emerson,Jon Rink,Jasper Lee,Yang Eric Li
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2023-10-12
卷期号:382 (6667)
被引量:85
标识
DOI:10.1126/science.adf5357
摘要
Delineating the gene-regulatory programs underlying complex cell types is fundamental for understanding brain function in health and disease. Here, we comprehensively examined human brain cell epigenomes by probing DNA methylation and chromatin conformation at single-cell resolution in 517 thousand cells (399 thousand neurons and 118 thousand non-neurons) from 46 regions of three adult male brains. We identified 188 cell types and characterized their molecular signatures. Integrative analyses revealed concordant changes in DNA methylation, chromatin accessibility, chromatin organization, and gene expression across cell types, cortical areas, and basal ganglia structures. We further developed single-cell methylation barcodes that reliably predict brain cell types using the methylation status of select genomic sites. This multimodal epigenomic brain cell atlas provides new insights into the complexity of cell-type-specific gene regulation in adult human brains.
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