@article {23324,
	title = {Developing novel methods to image and visualize 3D genomes},
	journal = {Cell Biology and Toxicology},
	volume = {34},
	year = {2018},
	note = {Sp. Iss. SIGr8snTimes Cited:14Cited References Count:80},
	month = {Oct},
	pages = {367-380},
	abstract = {To investigate three-dimensional (3D) genome organization in prokaryotic and eukaryotic cells, three main strategies are employed, namely nuclear proximity ligation-based methods, imaging tools (such as fluorescence in situ hybridization (FISH) and its derivatives), and computational/visualization methods. Proximity ligation-based methods are based on digestion and re-ligation of physically proximal cross-linked chromatin fragments accompanied by massively parallel DNA sequencing to measure the relative spatial proximity between genomic loci. Imaging tools enable direct visualization and quantification of spatial distances between genomic loci, and advanced implementation of (super-resolution) microscopy helps to significantly improve the resolution of images. Computational methods are used to map global 3D genome structures at various scales driven by experimental data, and visualization methods are used to visualize genome 3D structures in virtual 3D space-based on algorithms. In this review, we focus on the introduction of novel imaging and visualization methods to study 3D genomes. First, we introduce the progress made recently in 3D genome imaging in both fixed cell and live cells based on long-probe labeling, short-probe labeling, RNA FISH, and the CRISPR system. As the fluorescence-capturing capability of a particular microscope is very important for the sensitivity of bioimaging experiments, we also introduce two novel super-resolution microscopy methods, SDOM and low-power super-resolution STED, which have potential for time-lapse super-resolution live-cell imaging of chromatin. Finally, we review some software tools developed recently to visualize proximity ligation-based data. The imaging and visualization methods are complementary to each other, and all three strategies are not mutually exclusive. These methods provide powerful tools to explore the mechanisms of gene regulation and transcription in cell nuclei.},
	keywords = {architecture},
	isbn = {0742-2091},
	doi = {10.1007/s10565-018-9427-z},
	url = {\&lt;Go to ISI\&gt;://WOS:000442997300004},
	author = {Ma, T. S. and L. Chen and Shi, M. X. and Niu, J. and X. Zhang and Yang, X. S. and Zhanghao, K. and Wang, M. Y. and Xi, P. and Jin, D. Y. and Zhang, M. and Gao, J. T.}
}
