CENP-E combines a slow, processive motor and a flexible coiled coil to produce an essential motile kinetochore tether

J Cell Biol. 2008 May 5;181(3):411-9. doi: 10.1083/jcb.200802189. Epub 2008 Apr 28.

Abstract

The mitotic kinesin centromere protein E (CENP-E) is an essential kinetochore component that directly contributes to the capture and stabilization of spindle microtubules by kinetochores. Although reduction in CENP-E leads to high rates of whole chromosome missegregation, neither its properties as a microtubule-dependent motor nor how it contributes to the dynamic linkage between kinetochores and microtubules is known. Using single-molecule assays, we demonstrate that CENP-E is a very slow, highly processive motor that maintains microtubule attachment for long periods. Direct visualization of full-length Xenopus laevis CENP-E reveals a highly flexible 230-nm coiled coil separating its kinetochore-binding and motor domains. We also show that full-length CENP-E is a slow plus end-directed motor whose activity is essential for metaphase chromosome alignment. We propose that the highly processive microtubule-dependent motor activity of CENP-E serves to power chromosome congression and provides a flexible, motile tether linking kinetochores to dynamic spindle microtubules.

Publication types

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

MeSH terms

  • Animals
  • Chromosomal Proteins, Non-Histone / chemistry*
  • Chromosomal Proteins, Non-Histone / genetics
  • Chromosomal Proteins, Non-Histone / metabolism
  • Chromosome Segregation
  • Kinetochores / chemistry*
  • Kinetochores / metabolism
  • Microtubules / chemistry*
  • Microtubules / metabolism
  • Models, Biological
  • Molecular Motor Proteins / chemistry*
  • Molecular Motor Proteins / genetics
  • Molecular Motor Proteins / metabolism
  • Protein Structure, Secondary*
  • Recombinant Fusion Proteins / chemistry
  • Recombinant Fusion Proteins / genetics
  • Recombinant Fusion Proteins / metabolism
  • Spindle Apparatus / chemistry*
  • Spindle Apparatus / metabolism
  • Xenopus Proteins / chemistry
  • Xenopus Proteins / genetics
  • Xenopus Proteins / metabolism
  • Xenopus laevis

Substances

  • Chromosomal Proteins, Non-Histone
  • Molecular Motor Proteins
  • Recombinant Fusion Proteins
  • Xenopus Proteins
  • centromere protein E