Current working models of SMC-driven DNA-loop extrusion

Biochem Soc Trans. 2023 Oct 31;51(5):1801-1810. doi: 10.1042/BST20220898.

Abstract

Structural maintenance of chromosome (SMC) proteins play a key roles in the chromosome organization by condensing two meters of DNA into cell-sized structures considered as the SMC protein extrudes DNA loop. Recent sequencing-based high-throughput chromosome conformation capture technique (Hi-C) and single-molecule experiments have provided direct evidence of DNA-loop extrusion. However, the molecular mechanism by which SMCs extrude a DNA loop is still under debate. Here, we review DNA-loop extrusion studies with single-molecule assays and introduce recent structural studies of how the ATP-hydrolysis cycle is coupled to the conformational changes of SMCs for DNA-loop extrusion. In addition, we explain the conservation of the DNA-binding sites that are vital for dynamic DNA-loop extrusion by comparing Cryo-EM structures of SMC complexes. Based on this information, we compare and discuss four compelling working models that explain how the SMC complex extrudes a DNA loop.

Keywords: Brownian-ratchet model; DNA loop extrusion; DNA-segment capture/DNA pumping model; SMC; hold-and-feed model; scrunching model.

Publication types

  • Review
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bacterial Proteins* / metabolism
  • Binding Sites
  • Cell Cycle Proteins / metabolism
  • Chromosomes / metabolism
  • DNA / chemistry
  • Multiprotein Complexes* / chemistry

Substances

  • Multiprotein Complexes
  • Bacterial Proteins
  • DNA
  • Cell Cycle Proteins