| Literature DB >> 34483043 |
Brandon M Pratt1, Hyejung Won2.
Abstract
Understanding the exquisitely complex nature of the three-dimensional organization of the genome and how it affects gene regulation remains a central question in biology. Recent advances in sequencing- and imaging-based approaches in decoding the three-dimensional chromatin landscape have enabled a systematic characterization of gene regulatory architecture. In this review, we outline how chromatin architecture provides a reference atlas to predict the functional consequences of non-coding variants associated with human traits and disease. High-throughput perturbation assays such as massively parallel reporter assays (MPRA) and CRISPR-based genome engineering in combination with a reference atlas opened an avenue for going beyond observational studies to experimentally validating the regulatory principles of the genome. We conclude by providing a suggested path forward by calling attention to barriers that can be addressed for a more complete understanding of the regulatory landscape of the human brain. Published by Elsevier Ltd.Entities:
Keywords: Chromatin architecture; GWAS; Gene regulatory landscape; Hi-C; SNP-gene relationship; Variant effects on gene regulation
Mesh:
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Year: 2021 PMID: 34483043 PMCID: PMC8761161 DOI: 10.1016/j.semcdb.2021.08.013
Source DB: PubMed Journal: Semin Cell Dev Biol ISSN: 1084-9521 Impact factor: 7.727