Bacillus subtilis SMC complexes juxtapose chromosome arms as they travel from origin to terminus

Science. 2017 Feb 3;355(6324):524-527. doi: 10.1126/science.aai8982.

Abstract

Structural maintenance of chromosomes (SMC) complexes play critical roles in chromosome dynamics in virtually all organisms, but how they function remains poorly understood. In the bacterium Bacillus subtilis, SMC-condensin complexes are topologically loaded at centromeric sites adjacent to the replication origin. Here we provide evidence that these ring-shaped assemblies tether the left and right chromosome arms together while traveling from the origin to the terminus (>2 megabases) at rates >50 kilobases per minute. Condensin movement scales linearly with time, providing evidence for an active transport mechanism. These data support a model in which SMC complexes function by processively enlarging DNA loops. Loop formation followed by processive enlargement provides a mechanism by which condensin complexes compact and resolve sister chromatids in mitosis and by which cohesin generates topologically associating domains during interphase.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine Triphosphatases / metabolism*
  • Bacillus subtilis / genetics*
  • Bacillus subtilis / metabolism*
  • Bacterial Proteins / metabolism*
  • Cell Cycle Proteins / metabolism*
  • Chromosome Segregation
  • Chromosomes, Bacterial / chemistry
  • Chromosomes, Bacterial / metabolism*
  • DNA, Bacterial / chemistry
  • DNA, Bacterial / metabolism
  • DNA-Binding Proteins / metabolism*
  • Multiprotein Complexes / metabolism*

Substances

  • Bacterial Proteins
  • Cell Cycle Proteins
  • DNA, Bacterial
  • DNA-Binding Proteins
  • Multiprotein Complexes
  • SMC protein, Bacteria
  • condensin complexes
  • Adenosine Triphosphatases