A liquid-like spindle domain promotes acentrosomal spindle assembly in mammalian oocytes

Science. 2019 Jun 28;364(6447):eaat9557. doi: 10.1126/science.aat9557.

Abstract

Mammalian oocytes segregate chromosomes with a microtubule spindle that lacks centrosomes, but the mechanisms by which acentrosomal spindles are organized and function are largely unclear. In this study, we identify a conserved subcellular structure in mammalian oocytes that forms by phase separation. This structure, which we term the liquid-like meiotic spindle domain (LISD), permeates the spindle poles and forms dynamic protrusions that extend well beyond the spindle. The LISD selectively concentrates multiple microtubule regulatory factors and allows them to diffuse rapidly within the spindle volume. Disruption of the LISD via different means disperses these factors and leads to severe spindle assembly defects. Our data suggest a model whereby the LISD promotes meiotic spindle assembly by serving as a reservoir that sequesters and mobilizes microtubule regulatory factors in proximity to spindle microtubules.

Publication types

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

MeSH terms

  • Animals
  • Aurora Kinase A / metabolism
  • Centrosome / physiology*
  • Clathrin Heavy Chains / metabolism
  • Female
  • Fetal Proteins / metabolism
  • Meiosis*
  • Mice
  • Mice, Inbred C57BL
  • Microtubule-Associated Proteins / metabolism
  • Microtubules / physiology*
  • NIH 3T3 Cells
  • Oocytes / physiology*
  • Spindle Apparatus / physiology*

Substances

  • Fetal Proteins
  • Microtubule-Associated Proteins
  • TACC3 protein, mouse
  • Clathrin Heavy Chains
  • Aurora Kinase A