Cep55 regulates spindle organization and cell cycle progression in meiotic oocyte

Sci Rep. 2015 Nov 19:5:16978. doi: 10.1038/srep16978.

Abstract

Cep55 is a relatively novel member of the centrosomal protein family. Here, we show that Cep55 is expressed in mouse oocytes from the germinal vesicle (GV) to metaphase II (MII) stages. Immuostaining and confocal microscopy as well as time lapse live imaging after injection of mRNA encoding fusion protein of Cep55 and GFP identified that Cep55 was localized to the meiotic spindle, especially to the spindle poles at metaphase, while it was concentrated at the midbody in telophase in meiotic oocytes. Knockdown of Cep55 by specific siRNA injection caused the dissociation of γ-tubulin from the spindle poles, resulting in severely defective spindles and misaligned chromosomes, leading to metaphase I arrest and failure of first polar body (PB1) extrusion. Correspondingly, cyclin B accumulation and spindle assembly checkpoint (SAC) activation were observed in Cep55 knockdown oocytes. Our results suggest that Cep55 may act as an MTOC-associated protein regulating spindle organization, and thus cell cycle progression during mouse oocyte meiotic maturation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anaphase
  • Animals
  • Cell Cycle Proteins / metabolism*
  • Cell Cycle*
  • Chromosomes, Mammalian / metabolism
  • Cyclin B1 / metabolism
  • Female
  • Gene Knockdown Techniques
  • M Phase Cell Cycle Checkpoints
  • Mice
  • Oocytes / cytology*
  • Oocytes / metabolism*
  • Polar Bodies / metabolism
  • Protein Transport
  • Spindle Apparatus / metabolism*
  • Subcellular Fractions / metabolism
  • Tubulin / metabolism

Substances

  • Cell Cycle Proteins
  • Cep55 protein, mouse
  • Cyclin B1
  • Tubulin