Research

Active enhancers strengthen insulation by RNA-mediated CTCF binding at chromatin domain boundaries

    • 1National Center for Biological Sciences, Tata Institute for Fundamental Research, Bangalore, Karnataka 560065, India;
    • 2Sastra Deemed University, Thanjavur, Tamil Nadu 613401, India;
    • 3The University of Trans-Disciplinary Health Sciences and Technology, Bangalore, Karnataka 560064, India;
    • 4Department of Biology, Emory University, Atlanta, Georgia 30322, USA;
    • 5Basic Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, Washington 98109, USA
    • 6 These authors contributed equally to this work.
Published January 17, 2023. https://doi.org/10.1101/gr.276643.122
Download PDF Cite Article Permissions Share
cover of Genome Research Vol 36 Issue 11
Current Issue:

Abstract

Vertebrate genomes are partitioned into chromatin domains or topologically associating domains (TADs), which are typically bound by head-to-head pairs of CTCF binding sites. Transcription at domain boundaries correlates with better insulation; however, it is not known whether the boundary transcripts themselves contribute to boundary function. Here we characterize boundary-associated RNAs genome-wide, focusing on the disease-relevant INK4a/ARF and MYC TAD. Using CTCF site deletions and boundary-associated RNA knockdowns, we observe that boundary-associated RNAs facilitate recruitment and clustering of CTCF at TAD borders. The resulting CTCF enrichment enhances TAD insulation, enhancer–promoter interactions, and TAD gene expression. Importantly, knockdown of boundary-associated RNAs results in loss of boundary insulation function. Using enhancer deletions and CRISPRi of promoters, we show that active TAD enhancers, but not promoters, induce boundary-associated RNA transcription, thus defining a novel class of regulatory enhancer RNAs.


Notes

[1] Supplementary material [Supplemental material is available for this article.]

[2] Article published online before print. Article, supplemental material, and publication date are at https://www.genome.org/cgi/doi/10.1101/gr.276643.122.

[3] Freely available online through the Genome Research Open Access option.

Loading
Loading
Loading
Back to top