Shim Sang-Hee
Department of Chemistry, Korea University, Seoul, 02481, Korea.
Genes Genomics. 2021 Mar;43(3):281-287. doi: 10.1007/s13258-021-01044-9. Epub 2021 Feb 25.
Recent advancements in sequencing and imaging technologies are providing new perspectives in solving the mystery of three-dimensional folding of genome in a nucleus. Chromosome conformation capture sequencing has discovered new chromatin structures such as topologically associated domains and loops in hundreds of kilobases. Super-resolution fluorescence microscopy with nanometer resolutions, in particular multiplexed approaches with sequence-specificity, has visualized chromatin structures from the rough folds of whole chromosomes to the fine loops of cis-regulatory elements in intact individual nuclei. Here, recent advancements in genome visualization tools with highly multiplexed labeling and reading are introduced. These imaging technologies have found ensemble behavior consistent to sequencing results, while unveiling single-cell variations. But, they also generated contradictory results on the roles of architectural proteins (like cohesion and CTCF) and enhancer-promoter interactions. Live-cell labeling methods for imaging specific genomic loci, especially the CRISPR/dCas9 system, are reviewed in order to give perspectives in the emergence of tools for visualizing genome structural dynamics.
测序和成像技术的最新进展为解决细胞核中基因组三维折叠之谜提供了新视角。染色体构象捕获测序发现了新的染色质结构,如数百千碱基对中的拓扑相关结构域和环。具有纳米分辨率的超分辨率荧光显微镜,特别是具有序列特异性的多重方法,已经可视化了从完整单个细胞核中全染色体的粗略折叠到顺式调控元件的精细环的染色质结构。在此,介绍了具有高度多重标记和读取功能的基因组可视化工具的最新进展。这些成像技术发现了与测序结果一致的整体行为,同时揭示了单细胞变异。但是,它们在结构蛋白(如黏连蛋白和CTCF)的作用以及增强子-启动子相互作用方面也产生了相互矛盾的结果。为了展望可视化基因组结构动力学工具的出现,对用于成像特定基因组位点的活细胞标记方法,尤其是CRISPR/dCas9系统进行了综述。