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Genome-wide Chromatin State Transitions Associated with Developmental and Environmental Cues
Author(s) -
Jiang Zhu,
Mazhar Adli,
James Zou,
Griet Verstappen,
Michael J. Coyne,
Xiaolan Zhang,
Timothy Durham,
Mohammad Reza Miri,
Vikram Deshpande,
Philip L. De Jager,
David A. Bennett,
Joseph A. Houmard,
Deborah M. Muoio,
Tamer T. Önder,
Ray Camahort,
Chad A. Cowan,
Alexander Meissner,
Charles B. Epstein,
Noam Shoresh,
B Bernstein
Publication year - 2013
Publication title -
cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 26.304
H-Index - 776
eISSN - 1097-4172
pISSN - 0092-8674
DOI - 10.1016/j.cell.2012.12.033
Subject(s) - biology , chromatin , epigenome , reprogramming , genome , genetics , evolutionary biology , chromatin remodeling , epigenetics , heterochromatin , chia pet , computational biology , genomic organization , replication timing , dna methylation , cell , gene , gene expression
Differences in chromatin organization are key to the multiplicity of cell states that arise from a single genetic background, yet the landscapes of in vivo tissues remain largely uncharted. Here, we mapped chromatin genome-wide in a large and diverse collection of human tissues and stem cells. The maps yield unprecedented annotations of functional genomic elements and their regulation across developmental stages, lineages, and cellular environments. They also reveal global features of the epigenome, related to nuclear architecture, that also vary across cellular phenotypes. Specifically, developmental specification is accompanied by progressive chromatin restriction as the default state transitions from dynamic remodeling to generalized compaction. Exposure to serum in vitro triggers a distinct transition that involves de novo establishment of domains with features of constitutive heterochromatin. We describe how these global chromatin state transitions relate to chromosome and nuclear architecture, and discuss their implications for lineage fidelity, cellular senescence, and reprogramming.

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