表观遗传学
染色质
生物
电池类型
细胞生物学
基因表达
背景(考古学)
基因组学
计算生物学
DNA甲基化
细胞
基因
表观遗传学
遗传学
细胞核
基因组
古生物学
作者
Yodai Takei,Shiwei Zheng,Jina Yun,Sheel Shah,Nico Pierson,Jonathan A. White,Simone Schindler,Carsten H. Tischbirek,Guo‐Cheng Yuan,Long Cai
出处
期刊:Science
[American Association for the Advancement of Science (AAAS)]
日期:2021-09-30
卷期号:374 (6567): 586-594
被引量:99
标识
DOI:10.1126/science.abj1966
摘要
Diverse cell types in tissues have distinct gene expression programs, chromatin states, and nuclear architectures. To correlate such multimodal information across thousands of single cells in mouse brain tissue sections, we use integrated spatial genomics, imaging thousands of genomic loci along with RNAs and epigenetic markers simultaneously in individual cells. We reveal that cell type–specific association and scaffolding of DNA loci around nuclear bodies organize the nuclear architecture and correlate with differential expression levels in different cell types. At the submegabase level, active and inactive X chromosomes access similar domain structures in single cells despite distinct epigenetic and expression states. This work represents a major step forward in linking single-cell three-dimensional nuclear architecture, gene expression, and epigenetic modifications in a native tissue context.
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