| Literature DB >> 34789882 |
Warren Winick-Ng1, Alexander Kukalev2, Izabela Harabula2,3, Luna Zea-Redondo2,3, Dominik Szabó2,3, Mandy Meijer4, Leonid Serebreni2,5, Yingnan Zhang6, Simona Bianco7, Andrea M Chiariello7, Ibai Irastorza-Azcarate2, Christoph J Thieme2, Thomas M Sparks2, Sílvia Carvalho2,8,9,10, Luca Fiorillo7, Francesco Musella7, Ehsan Irani2,11, Elena Torlai Triglia2,12, Aleksandra A Kolodziejczyk13,14,15, Andreas Abentung16,17, Galina Apostolova16, Eleanor J Paul18,19,20, Vedran Franke21, Rieke Kempfer2,3, Altuna Akalin21, Sarah A Teichmann13,14, Georg Dechant16, Mark A Ungless18, Mario Nicodemi7,11, Lonnie Welch6, Gonçalo Castelo-Branco4,22, Ana Pombo23,24,25.
Abstract
The three-dimensional (3D) structure of chromatin is intrinsically associated with gene regulation and cell function1-3. Methods based on chromatin conformation capture have mapped chromatin structures in neuronal systems such as in vitro differentiated neurons, neurons isolated through fluorescence-activated cell sorting from cortical tissues pooled from different animals and from dissociated whole hippocampi4-6. However, changes in chromatin organization captured by imaging, such as the relocation of Bdnf away from the nuclear periphery after activation7, are invisible with such approaches8. Here we developed immunoGAM, an extension of genome architecture mapping (GAM)2,9, to map 3D chromatin topology genome-wide in specific brain cell types, without tissue disruption, from single animals. GAM is a ligation-free technology that maps genome topology by sequencing the DNA content from thin (about 220 nm) nuclear cryosections. Chromatin interactions are identified from the increased probability of co-segregation of contacting loci across a collection of nuclear slices. ImmunoGAM expands the scope of GAM to enable the selection of specific cell types using low cell numbers (approximately 1,000 cells) within a complex tissue and avoids tissue dissociation2,10. We report cell-type specialized 3D chromatin structures at multiple genomic scales that relate to patterns of gene expression. We discover extensive 'melting' of long genes when they are highly expressed and/or have high chromatin accessibility. The contacts most specific of neuron subtypes contain genes associated with specialized processes, such as addiction and synaptic plasticity, which harbour putative binding sites for neuronal transcription factors within accessible chromatin regions. Moreover, sensory receptor genes are preferentially found in heterochromatic compartments in brain cells, which establish strong contacts across tens of megabases. Our results demonstrate that highly specific chromatin conformations in brain cells are tightly related to gene regulation mechanisms and specialized functions.Entities:
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Year: 2021 PMID: 34789882 PMCID: PMC8612935 DOI: 10.1038/s41586-021-04081-2
Source DB: PubMed Journal: Nature ISSN: 0028-0836 Impact factor: 49.962