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基于显微镜的染色体构象捕获技术使我们能够在完整的生物体中同时观察基因组组织和转录。

Microscopy-Based Chromosome Conformation Capture Enables Simultaneous Visualization of Genome Organization and Transcription in Intact Organisms.

机构信息

Centre de Biochimie Structurale, CNRS UMR 5048, INSERM U1054, Université de Montpellier, 60 rue de Navacelles, 34090 Montpellier, France.

Institut de Génétique Humaine, CNRS UMR 9002, Université de Montpellier, 141 rue de la Cardonille, 34396 Montpellier, France.

出版信息

Mol Cell. 2019 Apr 4;74(1):212-222.e5. doi: 10.1016/j.molcel.2019.01.011. Epub 2019 Feb 19.

DOI:10.1016/j.molcel.2019.01.011
PMID:30795893
Abstract

Eukaryotic chromosomes are organized in multiple scales, from nucleosomes to chromosome territories. Recently, genome-wide methods identified an intermediate level of chromosome organization, topologically associating domains (TADs), that play key roles in transcriptional regulation. However, these methods cannot directly examine the interplay between transcriptional activation and chromosome architecture while maintaining spatial information. Here we present a multiplexed, sequential imaging approach (Hi-M) that permits simultaneous detection of chromosome organization and transcription in single nuclei. This allowed us to unveil the changes in 3D chromatin organization occurring upon transcriptional activation and homologous chromosome unpairing during awakening of the zygotic genome in intact Drosophila embryos. Excitingly, the ability of Hi-M to explore the multi-scale chromosome architecture with spatial resolution at different stages of development or during the cell cycle will be key to understanding the mechanisms and consequences of the 4D organization of the genome.

摘要

真核染色体在多个尺度上进行组织,从核小体到染色体区域。最近,全基因组方法鉴定出了染色体组织的一个中间水平,即拓扑关联结构域(TADs),它们在转录调控中发挥关键作用。然而,这些方法不能在保持空间信息的同时,直接研究转录激活和染色体结构之间的相互作用。在这里,我们提出了一种多重、顺序成像方法(Hi-M),可以在单个核中同时检测染色体组织和转录。这使我们能够揭示在完整的果蝇胚胎中,合子基因组激活以及同源染色体解联会过程中,转录激活时三维染色质组织发生的变化。令人兴奋的是,Hi-M 能够以空间分辨率在不同发育阶段或细胞周期探索多尺度染色体结构的能力,对于理解基因组的 4D 组织的机制和后果将是关键。

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