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Tissue-specific analysis of chromatin state identifies temporal signatures of enhancer activity during embryonic development

Item Type:Article
Title:Tissue-specific analysis of chromatin state identifies temporal signatures of enhancer activity during embryonic development
Creators Name:Bonn, S. and Zinzen, R.P. and Girardot, C. and Gustafson, E.H. and Perez-Gonzalez, A. and Delhomme, N. and Ghavi-Helm, Y. and Wilczynski, B. and Riddell, A. and Furlong, E.E.
Abstract:Chromatin modifications are associated with many aspects of gene expression, yet their role in cellular transitions during development remains elusive. Here, we use a new approach to obtain cell type-specific information on chromatin state and RNA polymerase II (Pol II) occupancy within the multicellular Drosophila melanogaster embryo. We directly assessed the relationship between chromatin modifications and the spatio-temporal activity of enhancers. Rather than having a unique chromatin state, active developmental enhancers show heterogeneous histone modifications and Pol II occupancy. Despite this complexity, combined chromatin signatures and Pol II presence are sufficient to predict enhancer activity de novo. Pol II recruitment is highly predictive of the timing of enhancer activity and seems dependent on the timing and location of transcription factor binding. Chromatin modifications typically demarcate large regulatory regions encompassing multiple enhancers, whereas local changes in nucleosome positioning and Pol II occupancy delineate single active enhancers. This cell type-specific view identifies dynamic enhancer usage, an essential step in deciphering developmental networks.
Keywords:Chromatin, Chromatin Immunoprecipitation, Developmental Gene Expression Regulation, Embryonic Development, Genetic Enhancer Elements, Histones, RNA Polymerase II, Transcription Factors, Animals, Drosophila melanogaster
Source:Nature Genetics
ISSN:1061-4036
Publisher:Nature Publishing Group
Volume:44
Number:2
Page Range:148-156
Date:February 2012
Official Publication:https://doi.org/10.1038/ng.1064
PubMed:View item in PubMed

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