Coordinated Effects of Sequence Variation on DNA Binding, Chromatin Structure, and Transcription

Helena Kilpinen(University of Geneva), Sebastian M. Waszak(SIB Swiss Institute of Bioinformatics), Andreas R. Gschwind(SIB Swiss Institute of Bioinformatics), Sunil K. Raghav(École Polytechnique Fédérale de Lausanne), Robert M. Witwicki(University of Lausanne), Andrea Orioli(University of Lausanne), Eugenia Migliavacca(SIB Swiss Institute of Bioinformatics), Michael R. Wiederkehr(University of Lausanne), María Gutiérrez‐Arcelus(University of Geneva), Nikolaos I. Panousis(University of Geneva), Alisa Yurovsky(University of Geneva), Tuuli Lappalainen(University of Geneva), Luciana Romano-Palumbo(University of Geneva), Alexandra Planchon(University of Geneva), Deborah Bielser(University of Geneva), Julien Bryois(University of Geneva), Ismaël Padioleau(University of Geneva), Gilles Udin(École Polytechnique Fédérale de Lausanne), Sarah Thurnheer(Protein Express (United States)), David L. Hacker(Protein Express (United States)), Leighton J. Core(Cornell University), John T. Lis(Cornell University), Nouria Hernandez(University of Lausanne), Alexandre Reymond(University of Lausanne), Bart Deplancke(SIB Swiss Institute of Bioinformatics), Emmanouil T. Dermitzakis(University of Geneva)
Science
October 18, 2013
Cited by 383Open Access
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Abstract

DNA sequence variation has been associated with quantitative changes in molecular phenotypes such as gene expression, but its impact on chromatin states is poorly characterized. To understand the interplay between chromatin and genetic control of gene regulation, we quantified allelic variability in transcription factor binding, histone modifications, and gene expression within humans. We found abundant allelic specificity in chromatin and extensive local, short-range, and long-range allelic coordination among the studied molecular phenotypes. We observed genetic influence on most of these phenotypes, with histone modifications exhibiting strong context-dependent behavior. Our results implicate transcription factors as primary mediators of sequence-specific regulation of gene expression programs, with histone modifications frequently reflecting the primary regulatory event.


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