» Articles » PMID: 37012454

Enhancer-promoter Contact Formation Requires RNAPII and Antagonizes Loop Extrusion

Overview
Journal Nat Genet
Specialty Genetics
Date 2023 Apr 3
PMID 37012454
Authors
Affiliations
Soon will be listed here.
Abstract

Homotypic chromatin interactions and loop extrusion are thought to be the two main drivers of mammalian chromosome folding. Here we tested the role of RNA polymerase II (RNAPII) across different scales of interphase chromatin organization in a cellular system allowing for its rapid, auxin-mediated degradation. We combined Micro-C and computational modeling to characterize subsets of loops differentially gained or lost upon RNAPII depletion. Gained loops, extrusion of which was antagonized by RNAPII, almost invariably formed by engaging new or rewired CTCF anchors. Lost loops selectively affected contacts between enhancers and promoters anchored by RNAPII, explaining the repression of most genes. Surprisingly, promoter-promoter interactions remained essentially unaffected by polymerase depletion, and cohesin occupancy was sustained. Together, our findings reconcile the role of RNAPII in transcription with its direct involvement in setting-up regulatory three-dimensional chromatin contacts genome wide, while also revealing an impact on cohesin loop extrusion.

Citing Articles

Post-mitotic transcriptional activation and 3D regulatory interactions show locus- and differentiation-specific sensitivity to cohesin depletion.

Lee U, Laguillo-Diego A, Wong W, Ni Z, Cheng L, Li J bioRxiv. 2025; .

PMID: 40034648 PMC: 11875242. DOI: 10.1101/2025.02.13.638153.


Interplay between CTCF-binding and CTCF-lacking regulatory elements in generating an architectural stripe at the Igh locus.

Ma F, Ollikainen N, Du H, Braikia F, Cui N, Bianchi A Nat Commun. 2025; 16(1):2148.

PMID: 40032827 PMC: 11876664. DOI: 10.1038/s41467-025-57373-w.


CTCF regulates global chromatin accessibility and transcription during rod photoreceptor development.

Chen D, Keremane S, Wang S, Lei E Proc Natl Acad Sci U S A. 2025; 122(9):e2416384122.

PMID: 39993185 PMC: 11892594. DOI: 10.1073/pnas.2416384122.


Increasingly efficient chromatin binding of cohesin and CTCF supports chromatin architecture formation during zebrafish embryogenesis.

Cossmann J, Kos P, Varamogianni-Mamatsi V, Assenheimer D, Bischof T, Kuhn T Nat Commun. 2025; 16(1):1833.

PMID: 39979259 PMC: 11842872. DOI: 10.1038/s41467-025-56889-5.


Liquid condensates: a new barrier to loop extrusion?.

Selivanovskiy A, Molodova M, Khrameeva E, Ulianov S, Razin S Cell Mol Life Sci. 2025; 82(1):80.

PMID: 39976773 PMC: 11842697. DOI: 10.1007/s00018-024-05559-8.


References
1.
Aboelnour E, Bonev B . Decoding the organization, dynamics, and function of the 4D genome. Dev Cell. 2021; 56(11):1562-1573. DOI: 10.1016/j.devcel.2021.04.023. View

2.
Razin S, Kantidze O . The twisted path of the 3D genome: where does it lead?. Trends Biochem Sci. 2022; 47(9):736-744. DOI: 10.1016/j.tibs.2022.04.006. View

3.
Xiang J, Corces V . Regulation of 3D chromatin organization by CTCF. Curr Opin Genet Dev. 2020; 67:33-40. PMC: 8084898. DOI: 10.1016/j.gde.2020.10.005. View

4.
van Ruiten M, Rowland B . On the choreography of genome folding: A grand pas de deux of cohesin and CTCF. Curr Opin Cell Biol. 2021; 70:84-90. DOI: 10.1016/j.ceb.2020.12.001. View

5.
Beagan J, Phillips-Cremins J . On the existence and functionality of topologically associating domains. Nat Genet. 2020; 52(1):8-16. PMC: 7567612. DOI: 10.1038/s41588-019-0561-1. View