4.7 Review

Chromatin accessibility and the regulatory epigenome

Journal

NATURE REVIEWS GENETICS
Volume 20, Issue 4, Pages 207-220

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/s41576-018-0089-8

Keywords

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Funding

  1. NIH [P50HG007735, UM1HG009442, U19AI057266, 1UM1HG009436]
  2. Rita Allen Foundation
  3. Baxter Foundation Faculty Scholar Grant
  4. Human Frontiers Science Program grant [RGY006S]
  5. Chan Zuckerberg Initiative [2017-174468, 2018-182817]
  6. Ruth L. Kirschstein Institutional National Research Service Award (NRSA) [NIH 5 T32 HG000044]
  7. [EMBO ALTF 1119-2016]
  8. [HFSP LT 000835/2017-L]

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Physical access to DNA is a highly dynamic property of chromatin that plays an essential role in establishing and maintaining cellular identity. The organization of accessible chromatin across the genome reflects a network of permissible physical interactions through which enhancers, promoters, insulators and chromatin-binding factors cooperatively regulate gene expression. This landscape of accessibility changes dynamically in response to both external stimuli and developmental cues, and emerging evidence suggests that homeostatic maintenance of accessibility is itself dynamically regulated through a competitive interplay between chromatin-binding factors and nucleosomes. In this Review, we examine how the accessible genome is measured and explore the role of transcription factors in initiating accessibility remodelling; our goal is to illustrate how chromatin accessibility defines regulatory elements within the genome and how these epigenetic features are dynamically established to control gene expression.

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