染色质
转座酶
基因组
生物
计算生物学
光激活定位显微镜
荧光原位杂交
荧光显微镜
显微镜
DNA
细胞生物学
基因
遗传学
超分辨显微术
转座因子
荧光
染色体
物理
光学
作者
Liangqi Xie,Peng Dong,Xingqi Chen,Tsung-Han S. Hsieh,Sambashiva Banala,Margherita De Marzio,Brian P. English,Yifeng Qi,Seol Kyoung Jung,Kyong-Rim Kieffer-Kwon,Wesley R. Legant,Anders S. Hansen,Anton Schulmann,Rafael Casellas,Bin Zhang,Eric Betzig,Luke D. Lavis,Howard Y. Chang,Robert Tjian,Zhe Liu
出处
期刊:Nature Methods
[Springer Nature]
日期:2020-03-16
卷期号:17 (4): 430-436
被引量:68
标识
DOI:10.1038/s41592-020-0775-2
摘要
To image the accessible genome at nanometer scale in situ, we developed three-dimensional assay for transposase-accessible chromatin-photoactivated localization microscopy (3D ATAC-PALM) that integrates an assay for transposase-accessible chromatin with visualization, PALM super-resolution imaging and lattice light-sheet microscopy. Multiplexed with oligopaint DNA-fluorescence in situ hybridization (FISH), RNA-FISH and protein fluorescence, 3D ATAC-PALM connected microscopy and genomic data, revealing spatially segregated accessible chromatin domains (ACDs) that enclose active chromatin and transcribed genes. Using these methods to analyze genetically perturbed cells, we demonstrated that genome architectural protein CTCF prevents excessive clustering of accessible chromatin and decompacts ACDs. These results highlight 3D ATAC-PALM as a useful tool to probe the structure and organizing mechanism of the genome.
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