A transcribed enhancer dictates mesendoderm specification in pluripotency

Michael Alexanian(University of Lausanne), Daniel Maric(University of Lausanne), Stephen P. Jenkinson(University of Bern), Marco Mina(SIB Swiss Institute of Bioinformatics), Clayton E. Friedman(The University of Queensland), Ching-Chia Ting(University of Lausanne), Rudi Micheletti(University of Lausanne), Isabelle Plaisance(University of Lausanne), Mohamed Nemir(University of Lausanne), Damien Maison(University of Lausanne), Jasmin Kernen(University of Bern), Iole Pezzuto(University of Lausanne), Dominic Villeneuve(University of Lausanne), Frédéric Burdet(SIB Swiss Institute of Bioinformatics), Mark Ibberson(SIB Swiss Institute of Bioinformatics), Stephen L. Leib(University of Bern), Nathan J. Palpant(The University of Queensland), Nouria Hernandez(University of Lausanne), Samir Ounzain(University Hospital of Lausanne), Thierry Pedrazzini(University of Lausanne)
Nature Communications
November 21, 2017
Cited by 80Open Access
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Abstract

Enhancers and long noncoding RNAs (lncRNAs) are key determinants of lineage specification during development. Here, we evaluate remodeling of the enhancer landscape and modulation of the lncRNA transcriptome during mesendoderm specification. We sort mesendodermal progenitors from differentiating embryonic stem cells (ESCs) according to Eomes expression, and find that enhancer usage is coordinated with mesendoderm-specific expression of key lineage-determining transcription factors. Many of these enhancers are associated with the expression of lncRNAs. Examination of ESC-specific enhancers interacting in three-dimensional space with mesendoderm-specifying transcription factor loci identifies MesEndoderm Transcriptional Enhancer Organizing Region (Meteor). Genetic and epigenetic manipulation of the Meteor enhancer reveal its indispensable role during mesendoderm specification and subsequent cardiogenic differentiation via transcription-independent and -dependent mechanisms. Interestingly, Meteor-deleted ESCs are epigenetically redirected towards neuroectodermal lineages. Loci, topologically associating a transcribed enhancer and its cognate protein coding gene, appear to represent therefore a class of genomic elements controlling developmental competence in pluripotency.


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