4.8 Article

MCM complexes are barriers that restrict cohesin-mediated loop extrusion

期刊

NATURE
卷 606, 期 7912, 页码 197-+

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NATURE PORTFOLIO
DOI: 10.1038/s41586-022-04730-0

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资金

  1. Austrian Science Fund (FWF) [W1238-B20]
  2. National Institutes of Health Common Fund 4D Nucleome Program [DK107980]
  3. Human Frontier Science Program [HFSP RGP0057/2018]
  4. Medical Research Council UK University Unit grant [MC_UU_00007/2]
  5. European Research Council (ERC) [ERC-StG-804098]
  6. German Research Foundation (DFG) [SFB863-111166240]
  7. Max Planck Society
  8. Boehringer Ingelheim
  9. Austrian Research Promotion Agency [FFG-878286]
  10. ERC [693949, 101020558, ERC-CoG-818556]
  11. HFSP [RGP0057/2018]
  12. Vienna Science and Technology Fund [LS19-029]
  13. Austrian Academy of Sciences
  14. European Research Council (ERC) [101020558, 693949] Funding Source: European Research Council (ERC)

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This study reveals that the minichromosome maintenance (MCM) complex acts as a barrier in G1 phase for loop extrusion, reducing the number of CTCF-anchored loops and weakening TAD boundary insulation. The study also demonstrates that MCMs are physical barriers that frequently constrain cohesin translocation. The findings suggest that loop extrusion barriers, including MCMs, play a crucial role in shaping the three-dimensional genome.
Eukaryotic genomes are compacted into loops and topologically associating domains (TADs)(1-3), which contribute to transcription, recombination and genomic stability(4,5). Cohesin extrudes DNA into loops that are thought to lengthen until CTCF boundaries are encountered(6-12). Little is known about whether loop extrusion is impeded by DNA-bound machines. Here we show that the minichromosome maintenance (MCM) complex is a barrier that restricts loop extrusion in G1 phase. Single-nucleus Hi-C (high-resolution chromosome conformation capture) of mouse zygotes reveals that MCM loading reduces CTCF-anchored loops and decreases TAD boundary insulation, which suggests that loop extrusion is impeded before reaching CTCF. This effect extends to HCT116 cells, in which MCMs affect the number of CTCF-anchored loops and gene expression. Simulations suggest that MCMs are abundant, randomly positioned and partially permeable barriers. Single-molecule imaging shows that MCMs are physical barriers that frequently constrain cohesin translocation in vitro. Notably, chimeric yeast MCMs that contain a cohesin-interaction motif from human MCM3 induce cohesin pausing, indicating that MCMs are 'active' barriers with binding sites. These findings raise the possibility that cohesin can arrive by loop extrusion at MCMs, which determine the genomic sites at which sister chromatid cohesion is established. On the basis of in vivo, in silico and in vitro data, we conclude that distinct loop extrusion barriers shape the three-dimensional genome.

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