| Literature DB >> 30795893 |
Andrés M Cardozo Gizzi1, Diego I Cattoni1, Jean-Bernard Fiche1, Sergio M Espinola1, Julian Gurgo1, Olivier Messina1, Christophe Houbron1, Yuki Ogiyama2, Giorgio L Papadopoulos2, Giacomo Cavalli2, Mounia Lagha3, Marcelo Nollmann4.
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.Entities:
Keywords: Drosophila development; chromatin; chromosome conformation capture; fluorescence microscopy; fluorescent in situ hybridization; genome architecture; genome organization; oligopaint; topologically associating domains; transcriptional regulation
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Year: 2019 PMID: 30795893 DOI: 10.1016/j.molcel.2019.01.011
Source DB: PubMed Journal: Mol Cell ISSN: 1097-2765 Impact factor: 17.970