An atlas of lamina-associated chromatin across twelve human cell types reveals an intermediate chromatin subtype

Bibliographic Details
Title: An atlas of lamina-associated chromatin across twelve human cell types reveals an intermediate chromatin subtype
Authors: Parisha P. Shah, Kathleen C. Keough, Ketrin Gjoni, Garrett T. Santini, Richard J. Abdill, Nadeera M. Wickramasinghe, Carolyn E. Dundes, Ashley Karnay, Angela Chen, Rachel E. A. Salomon, Patrick J. Walsh, Son C. Nguyen, Sean Whalen, Eric F. Joyce, Kyle M. Loh, Nicole Dubois, Katherine S. Pollard, Rajan Jain
Source: Genome Biology, Vol 24, Iss 1, Pp 1-35 (2023)
Publisher Information: BMC, 2023.
Publication Year: 2023
Collection: LCC:Biology (General)
LCC:Genetics
Subject Terms: Lamina-associated domains, Peripheral chromatin organization, 3D genome, Cellular differentiation, Biology (General), QH301-705.5, Genetics, QH426-470
More Details: Abstract Background Association of chromatin with lamin proteins at the nuclear periphery has emerged as a potential mechanism to coordinate cell type-specific gene expression and maintain cellular identity via gene silencing. Unlike many histone modifications and chromatin-associated proteins, lamina-associated domains (LADs) are mapped genome-wide in relatively few genetically normal human cell types, which limits our understanding of the role peripheral chromatin plays in development and disease. Results To address this gap, we map LAMIN B1 occupancy across twelve human cell types encompassing pluripotent stem cells, intermediate progenitors, and differentiated cells from all three germ layers. Integrative analyses of this atlas with gene expression and repressive histone modification maps reveal that lamina-associated chromatin in all twelve cell types is organized into at least two subtypes defined by differences in LAMIN B1 occupancy, gene expression, chromatin accessibility, transposable elements, replication timing, and radial positioning. Imaging of fluorescently labeled DNA in single cells validates these subtypes and shows radial positioning of LADs with higher LAMIN B1 occupancy and heterochromatic histone modifications primarily embedded within the lamina. In contrast, the second subtype of lamina-associated chromatin is relatively gene dense, accessible, dynamic across development, and positioned adjacent to the lamina. Most genes gain or lose LAMIN B1 occupancy consistent with cell types along developmental trajectories; however, we also identify examples where the enhancer, but not the gene body and promoter, changes LAD state. Conclusions Altogether, this atlas represents the largest resource to date for peripheral chromatin organization studies and reveals an intermediate chromatin subtype.
Document Type: article
File Description: electronic resource
Language: English
ISSN: 1474-760X
Relation: https://doaj.org/toc/1474-760X
DOI: 10.1186/s13059-023-02849-5
Access URL: https://doaj.org/article/3460c0bf62da40d5bb6ad6b6c60d65c4
Accession Number: edsdoj.3460c0bf62da40d5bb6ad6b6c60d65c4
Database: Directory of Open Access Journals
More Details
ISSN:1474760X
DOI:10.1186/s13059-023-02849-5
Published in:Genome Biology
Language:English