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Epigenomic Co-localization and Co-evolution Reveal a Key Role for 5hmC as a Communication Hub in the Chromatin Network of ESCs

Authors :
David Ochoa
Daniel Rico
Juliane Perner
Ho-Ryun Chung
David Juan
Martin Vingron
Simone Marsili
Enrique Carrillo-de Santa Pau
Alfonso Valencia
Unión Europea. Comisión Europea. 7 Programa Marco
Source :
Cell Reports, Vol 14, Iss 5, Pp 1246-1257 (2016), Cell Reports, Repisalud, Instituto de Salud Carlos III (ISCIII), Europe PubMed Central
Publisher :
The Authors. Published by Elsevier Inc.

Abstract

Summary: Epigenetic communication through histone and cytosine modifications is essential for gene regulation and cell identity. Here, we propose a framework that is based on a chromatin communication model to get insight on the function of epigenetic modifications in ESCs. The epigenetic communication network was inferred from genome-wide location data plus extensive manual annotation. Notably, we found that 5-hydroxymethylcytosine (5hmC) is the most-influential hub of this network, connecting DNA demethylation to nucleosome remodeling complexes and to key transcription factors of pluripotency. Moreover, an evolutionary analysis revealed a central role of 5hmC in the co-evolution of chromatin-related proteins. Further analysis of regions where 5hmC co-localizes with specific interactors shows that each interaction points to chromatin remodeling, stemness, differentiation, or metabolism. Our results highlight the importance of cytosine modifications in the epigenetic communication of ESCs. : 5-hydroxymethylcytosine (5hmC) plays a key role in the epigenomic communication network of embryonic stem cells. Juan et al. build a communication network based in co-localization of epigenomic data and literature. The analysis of the network and its components reveals that proteins reading and editing 5hmC co-evolve and serve as links between diverse molecular processes.

Details

Language :
English
ISSN :
22111247
Issue :
5
Database :
OpenAIRE
Journal :
Cell Reports
Accession number :
edsair.doi.dedup.....8f0c1c2f32e043d63c3590f277e16e27
Full Text :
https://doi.org/10.1016/j.celrep.2016.01.008