Cited by 465Genomics and Chromatin DynamicsProtein Structure and DynamicsChromatin Remodeling and Cancer

The DOI matches its Crossref record; 76 of the 76 references it cites were found in a registry or an index; 8 of the 33 sources its claims cite were checked for support.

The structural basis for cohesin–CTCF-anchored loops

Open access
Li, Yan, Haarhuis, Judith H. I., Sedeño Cacciatore, Ángela, Oldenkamp, Roel, van Ruiten, Marjon S., Willems, Laureen, Teunissen, Hans, Muir, Kyle W., de Wit, Elzo, Rowland, Benjamin D., Panne, Daniel·2020·Nature

Abstract

Cohesin catalyses the folding of the genome into loops that are anchored by CTCF1. The molecular mechanism of how cohesin and CTCF structure the 3D genome has remained unclear. Here we show that a segment within the CTCF N terminus interacts with the SA2–SCC1 subunits of human cohesin. We report a crystal structure of SA2–SCC1 in complex with CTCF at a resolution of 2.7 Å, which reveals the molecular basis of the interaction. We demonstrate that this interaction is specifically required for CTCF-anchored loops and contributes to the positioning of cohesin at CTCF binding sites. A similar motif is present in a number of established and newly identified cohesin ligands, including the cohesin release factor WAPL2,3. Our data suggest that CTCF enables the formation of chromatin loops by protecting cohesin against loop release. These results provide fundamental insights into the molecular mechanism that enables the dynamic regulation of chromatin folding by cohesin and CTCF. The crystal structure of the SA2–SCC1 subunits of human cohesin in complex with CTCF reveals the molecular basis of the cohesin–CTCF interaction that enables the dynamic regulation of chromatin folding.

Overview

AI snapshot

Written from the paper’s full text.

TL;DR

CTCF’s N-terminal YxF motif binds the SA2–SCC1 “conserved essential surface” (CES), and a 2.6 Å crystal structure explains the interface. Disrupting this interface abolishes CTCF-anchored loops while leaving TAD-like structures largely present, suggesting CTCF stabilizes cohesin at loop anchors rather than merely acting as a passive barrier.

Key findings

  • CTCF residues 222–231 bind SA2–SCC1 with Kd = 1.04 ± 0.20 μM; Y226 and F228 are the lead anchoring residues, and Y226A/F228A abolish binding in GST pulldowns.
  • In HAP1 cells with endogenous CTCF Y226A F228A, Hi-C loop calls drop from 2756 in wild type to 98 in mutant cells; TAD-like structures remain but have less-clear edges.
  • FRAP shows cohesin is more mobile in CTCF Y226A F228A cells, and ChIP-qPCR/ChIP-seq show reduced cohesin at CTCF sites, while CTCF binding itself is largely unaffected.
  • WAPL competes with CTCF for the SA2–SCC1 CES; the CTCF peptide binds more strongly than WAPL peptides (WAPL 423–463 Kd ≈ 32.8 μM), and RNA-seq shows >2000 genes affected by the CTCF mutation.

Methods

  • Biochemical binding assays: GST pulldowns, isothermal titration calorimetry, and peptide arrays using SA2–SCC1 and mutant complexes.
  • Structural analysis: crystals of SA2–SCC1 in complex with a CTCF 222–231 peptide; structure determined by molecular replacement at 2.6 Å (Rwork/Rfree 0.25/0.27).
  • Cell and genome-wide assays: CRISPR/Cas9-generated HAP1 CTCF Y226A F228A cells, HaloTagged SCC1 FRAP, Hi-C, ChIP-qPCR/ChIP-seq, and RNA-seq.

Limitations

  • The paper does not include a dedicated limitations section.
  • Evident from the text: key cellular conclusions rely on the human haploid HAP1 cell line and a single CTCF interface mutant (Y226A F228A), with no in vivo organismal validation.
  • Evident from the text: CTCF depletion was lethal in both control and CTCF Y226A F228A HAP1 cells, so essential CTCF functions independent of CES engagement and CTCF-anchored loops remain unresolved.

Model-written summary. Check it against the paper before relying on it.

Integrity signals

Registry

Crossref · 10.1038/s41586-019-1910-z

Cites

76 of 76 references verified0 citation errors · 0 not checkable

Statistics

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Verification

Claims the paper makes

60 Own result · 16 Own method · 15 Own interpretation · 13 Not checked yet · 6 No basis given · 2 Partly supported · 1 Supported · accuracy not yet measured

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Show all 63 claims

  • It may state two separate claims as one. 24
  • Probably not a substantial claim. 25
  • The quote only partly states this claim. 16
50 of 50
  • The paper relies on this without support.

    TADs previously defined for wild type HAP1 cells are applicable to CTCF Y226A F228A cells for aggregate TAD analysis.

    “For this analysis we employed TADs previously defined for wild type HAP1 cells10.”
  • The paper relies on this without support.

    The non-diffusive fraction of SCC1-Halo fluorescence is a valid proxy for the chromatin-bound fraction of SCC1.

    “as a proxy for the chromatin-bound fraction of SCC1”
  • The paper relies on this without support.

    Histone H4 is a valid control for the chromatin fraction.

    “Histone H4 is used as a control for the chromatin fraction.”
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Metadata

Authors
Li, Y., Haarhuis, J. H. I., Sedeño Cacciatore, Á., Oldenkamp, R., van Ruiten, M. S., Willems, L., Teunissen, H., Muir, K. W., de Wit, E., Rowland, B. D., & Panne, D.
Affiliations
  • European Molecular Biology Laboratory (FR)
  • The Netherlands Cancer Institute (NL)
  • MRC Laboratory of Molecular Biology (GB)
  • University of Leicester (GB)
Corresponding author
  • Muir, Kyle W.
  • Rowland, Benjamin D.
  • Panne, Daniel
Venue
Nature
Published
2020-01-06
Volume
578
Issue
7795
Pages
472-476
ISSN
  • 0028-0836 (ISSN-L)
  • 1476-4687
OpenAlex
W2998399076
Cited by
459
References
75
Citations by year
2026: 55 · 2025: 70 · 2024: 84 · 2023: 75 · 2022: 70 · 2021: 63 · 2020: 42
FWCI
20.91
Type
journal article
Language
en
Open access
Locations
  • Nature (publishedVersion)
  • PubMed (publishedVersion)
  • PubMed Central (acceptedVersion)
  • RePEc: Research Papers in Economics (submittedVersion)
  • Figshare (submittedVersion, cc-by)
Funders
  • European Molecular Biology Laboratory (EMBL001)
  • Nederlandse Organisatie voor Wetenschappelijk Onderzoek (016.161.316)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Chromatin Dynamics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Protein Structure and Dynamics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Chromatin Remodeling and Cancer
Keywords
cohesin, CTCF, chromatin looping, 3D genome organization, protein-protein interaction, WAPL, chromatin folding, crystal structure
MeSH terms
CCCTC-Binding Factor, Cohesins, Binding Sites, Carrier Proteins, Chromatin, Chromosomal Proteins, Non-Histone, DNA, Humans, Ligands, Models, Molecular, Nuclear Proteins, Peptide Fragments, Protein Binding, Proto-Oncogene Proteins, Crystallography, X-Ray, Cell Cycle Proteins, Protein Subunits, Protein Stability

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