Mechanisms of spindle-pole organization are influenced by kinetochore activity in mammalian cells

Curr Biol. 2007 Feb 6;17(3):260-5. doi: 10.1016/j.cub.2006.11.071.

Abstract

The spindle is a fusiform bipolar-microtubule array that is responsible for chromosome segregation during mitosis. Focused poles are an essential feature of spindles in vertebrate somatic cells, and pole focusing has been shown to occur through a centrosome-independent self-organization mechanism where microtubule motors cross-link and focus microtubule minus ends. Most of our understanding of this mechanism for pole focusing derives from studies performed in cell-free extracts devoid of centrosomes and kinetochores. Here, we examine how sustained force from kinetochores influences the mechanism of pole focusing in cultured cells. We show that the motor-driven self-organization activities associated with NuMA (i.e., cytoplasmic dynein) and HSET are not necessary for pole focusing if sustained force from kinetochores is inhibited in Nuf2- or Mis12-deficient cells. Instead, pole organization relies on TPX2 as it cross-links spindle microtubules to centrosome-associated mitotic asters. Thus, both motor-driven and static-cross-linking mechanisms contribute to spindle-pole organization, and kinetochore activity influences the mechanism of spindle-pole organization. The motor-driven self-organization of microtubule minus ends at spindle poles is needed to organize spindle poles in vertebrate somatic cells when kinetochores actively exert force on spindle microtubules.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Antigens, Nuclear / metabolism
  • Cell Cycle Proteins / metabolism
  • Cell-Free System
  • Cells, Cultured
  • Green Fluorescent Proteins / metabolism
  • Humans
  • Kinetochores / metabolism*
  • Microtubule-Associated Proteins / metabolism
  • Microtubules / metabolism*
  • Mitosis
  • Nuclear Matrix-Associated Proteins / metabolism
  • Nuclear Proteins / metabolism
  • RNA, Small Interfering
  • Spindle Apparatus / metabolism*
  • Transfection

Substances

  • Antigens, Nuclear
  • Cell Cycle Proteins
  • MIS12 protein, human
  • Microtubule-Associated Proteins
  • NUF2 protein, human
  • NUMA1 protein, human
  • Nuclear Matrix-Associated Proteins
  • Nuclear Proteins
  • RNA, Small Interfering
  • TPX2 protein, human
  • Green Fluorescent Proteins