Actin-driven chromosomal motility leads to symmetry breaking in mammalian meiotic oocytes

Nat Cell Biol. 2008 Nov;10(11):1301-8. doi: 10.1038/ncb1788. Epub 2008 Oct 5.

Abstract

Movement of meiosis I (MI) chromosomes from the oocyte centre to a subcortical location is the first step in the establishment of cortical polarity. This is required for two consecutive rounds of asymmetric meiotic cell divisions, which generate a mature egg and two polar bodies. Here we use live-cell imaging and genetic and pharmacological manipulations to determine the force-generating mechanism underlying this chromosome movement. Chromosomes were observed to move toward the cortex in a pulsatile manner along a meandering path. This movement is not propelled by myosin-II-driven cortical flow but is associated with a cloud of dynamic actin filaments trailing behind the chromosomes/spindle. Formation of these filaments depends on the actin nucleation activity of Fmn2, a formin-family protein that concentrates around chromosomes through its amino-terminal region. Symmetry breaking of the actin cloud relative to chromosomes, and net chromosome translocation toward the cortex require actin turnover.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Actins / metabolism*
  • Actins / ultrastructure
  • Animals
  • Cell Polarity*
  • Cells, Cultured
  • Chromosomes, Mammalian / metabolism*
  • Female
  • Fluorescent Dyes / metabolism
  • Indoles / metabolism
  • Kinetics
  • Meiosis*
  • Mice
  • Mice, Inbred Strains
  • Microscopy, Video
  • Oocytes / metabolism*
  • Oocytes / ultrastructure

Substances

  • Actins
  • Fluorescent Dyes
  • Indoles
  • DAPI