| Literature DB >> 27210040 |
Haiyan Huang1, Qiang Wu2.
Abstract
The genomes are organized into ordered and hierarchical topological structures in interphase nuclei. Within discrete territories of each chromosome, topologically associated domains (TADs) play important roles in various nuclear processes such as gene regulation. Inside TADs separated by relatively constitutive boundaries, distal elements regulate their gene targets through specific chromatin-looping contacts such as long-distance enhancer-promoter interactions. High-throughput sequencing studies have revealed millions of potential regulatory DNA elements, which are much more abundant than the mere ∼20,000 genes they control. The recently emerged CRISPR-Cas9 genome editing technologies have enabled efficient and precise genetic and epigenetic manipulations of genomes. The multiplexed and high-throughput CRISPR capabilities facilitate the discovery and dissection of gene regulatory elements. Here, we describe the applications of CRISPR for genome, epigenome, and 3D genome editing, focusing on CRISPR DNA-fragment editing with Cas9 and a pair of sgRNAs to investigate topological folding of chromatin TADs and developmental gene regulation.Keywords: CTCF; Chromatin architecture; DNA-fragment editing; Enhancer; Insulator; Topological domain
Mesh:
Year: 2016 PMID: 27210040 DOI: 10.1016/j.jgg.2016.03.006
Source DB: PubMed Journal: J Genet Genomics ISSN: 1673-8527 Impact factor: 4.275