染色质
转座酶
表观遗传学
生物
基因组
计算生物学
背景(考古学)
染色体构象捕获
遗传学
DNA
基因
转座因子
DNA甲基化
基因表达
增强子
古生物学
作者
Xingqi Chen,Ying Shen,Will E. Draper,Jason D. Buenrostro,Ulrike M. Litzenburger,Seung Woo Cho,Ansuman T. Satpathy,Ava C. Carter,Rajarshi P. Ghosh,Alexandra East-Seletsky,Jennifer A. Doudna,William J. Greenleaf,Jan Liphardt,Howard Y. Chang
出处
期刊:Nature Methods
[Springer Nature]
日期:2016-10-17
卷期号:13 (12): 1013-1020
被引量:235
摘要
Spatial organization of the genome plays a central role in gene expression, DNA replication, and repair. But current epigenomic approaches largely map DNA regulatory elements outside of the native context of the nucleus. Here we report assay of transposase-accessible chromatin with visualization (ATAC-see), a transposase-mediated imaging technology that employs direct imaging of the accessible genome in situ, cell sorting, and deep sequencing to reveal the identity of the imaged elements. ATAC-see revealed the cell-type-specific spatial organization of the accessible genome and the coordinated process of neutrophil chromatin extrusion, termed NETosis. Integration of ATAC-see with flow cytometry enables automated quantitation and prospective cell isolation as a function of chromatin accessibility, and it reveals a cell-cycle dependence of chromatin accessibility that is especially dynamic in G1 phase. The integration of imaging and epigenomics provides a general and scalable approach for deciphering the spatiotemporal architecture of gene control.
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