| Literature DB >> 25959774 |
Darío G Lupiáñez1, Katerina Kraft1, Verena Heinrich2, Peter Krawitz1, Francesco Brancati3, Eva Klopocki4, Denise Horn2, Hülya Kayserili5, John M Opitz6, Renata Laxova6, Fernando Santos-Simarro7, Brigitte Gilbert-Dussardier8, Lars Wittler9, Marina Borschiwer10, Stefan A Haas11, Marco Osterwalder12, Martin Franke1, Bernd Timmermann13, Jochen Hecht14, Malte Spielmann15, Axel Visel16, Stefan Mundlos17.
Abstract
Mammalian genomes are organized into megabase-scale topologically associated domains (TADs). We demonstrate that disruption of TADs can rewire long-range regulatory architecture and result in pathogenic phenotypes. We show that distinct human limb malformations are caused by deletions, inversions, or duplications altering the structure of the TAD-spanning WNT6/IHH/EPHA4/PAX3 locus. Using CRISPR/Cas genome editing, we generated mice with corresponding rearrangements. Both in mouse limb tissue and patient-derived fibroblasts, disease-relevant structural changes cause ectopic interactions between promoters and non-coding DNA, and a cluster of limb enhancers normally associated with Epha4 is misplaced relative to TAD boundaries and drives ectopic limb expression of another gene in the locus. This rewiring occurred only if the variant disrupted a CTCF-associated boundary domain. Our results demonstrate the functional importance of TADs for orchestrating gene expression via genome architecture and indicate criteria for predicting the pathogenicity of human structural variants, particularly in non-coding regions of the human genome.Entities:
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Year: 2015 PMID: 25959774 PMCID: PMC4791538 DOI: 10.1016/j.cell.2015.04.004
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582