| Literature DB >> 34856126 |
Hyun Jung Oh1, Rodrigo Aguilar1, Barry Kesner1, Hun-Goo Lee1, Andrea J Kriz1, Hsueh-Ping Chu1, Jeannie T Lee2.
Abstract
Chromosome loops shift dynamically during development, homeostasis, and disease. CCCTC-binding factor (CTCF) is known to anchor loops and construct 3D genomes, but how anchor sites are selected is not yet understood. Here, we unveil Jpx RNA as a determinant of anchor selectivity. Jpx RNA targets thousands of genomic sites, preferentially binding promoters of active genes. Depleting Jpx RNA causes ectopic CTCF binding, massive shifts in chromosome looping, and downregulation of >700 Jpx target genes. Without Jpx, thousands of lost loops are replaced by de novo loops anchored by ectopic CTCF sites. Although Jpx controls CTCF binding on a genome-wide basis, it acts selectively at the subset of developmentally sensitive CTCF sites. Specifically, Jpx targets low-affinity CTCF motifs and displaces CTCF protein through competitive inhibition. We conclude that Jpx acts as a CTCF release factor and shapes the 3D genome by regulating anchor site usage.Entities:
Keywords: 3D genome; CTCF; CTCF release factor; CTCF site selection; Jpx RNA; chromatin loop; chromosome conformation; gene activation; loop anchors; noncoding RNA
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Year: 2021 PMID: 34856126 PMCID: PMC8671370 DOI: 10.1016/j.cell.2021.11.012
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582