AI Article Synopsis

  • Chromatin organization plays a crucial role in the diversity of cell states from a single genetic background, but many details remain unexplored in various human tissues.
  • This study provides comprehensive mappings of chromatin across different human tissues and stem cells, revealing important functional genomic elements and their regulation during development and in various cellular contexts.
  • Key findings indicate that as cells develop, chromatin becomes more restricted and compact, with significant changes occurring in response to external factors like serum, affecting chromatin architecture and influencing processes like lineage fidelity and cellular reprogramming.

Article Abstract

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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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3563935PMC
http://dx.doi.org/10.1016/j.cell.2012.12.033DOI Listing

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