Axin-1 Regulates Meiotic Spindle Organization in Mouse Oocytes

PLoS One. 2016 Jun 10;11(6):e0157197. doi: 10.1371/journal.pone.0157197. eCollection 2016.

Abstract

Axin-1, a negative regulator of Wnt signaling, is a versatile scaffold protein involved in centrosome separation and spindle assembly in mitosis, but its function in mammalian oogenesis remains unknown. Here we examined the localization and function of Axin-1 during meiotic maturation in mouse oocytes. Immunofluorescence analysis showed that Axin-1 was localized around the spindle. Knockdown of the Axin1 gene by microinjection of specific short interfering (si)RNA into the oocyte cytoplasm resulted in severely defective spindles, misaligned chromosomes, failure of first polar body (PB1) extrusion, and impaired pronuclear formation. However, supplementing the culture medium with the Wnt pathway activator LiCl improved spindle morphology and pronuclear formation. Downregulation of Axin1 gene expression also impaired the spindle pole localization of γ-tubulin/Nek9 and resulted in retention of the spindle assembly checkpoint protein BubR1 at kinetochores after 8.5 h of culture. Our results suggest that Axin-1 is critical for spindle organization and cell cycle progression during meiotic maturation in mouse oocytes.

MeSH terms

  • Animals
  • Axin Protein / analysis
  • Axin Protein / genetics
  • Axin Protein / metabolism*
  • Cell Cycle Proteins / analysis
  • Cell Cycle Proteins / metabolism
  • Cells, Cultured
  • Female
  • Meiosis*
  • Mice
  • NIMA-Related Kinases / analysis
  • NIMA-Related Kinases / metabolism
  • Oocytes / cytology*
  • Oocytes / metabolism
  • Oogenesis*
  • Protein Serine-Threonine Kinases / analysis
  • Protein Serine-Threonine Kinases / metabolism
  • RNA Interference
  • RNA, Small Interfering / genetics
  • Spindle Apparatus / genetics
  • Spindle Apparatus / metabolism
  • Spindle Apparatus / ultrastructure*
  • Tubulin / analysis
  • Tubulin / metabolism

Substances

  • Axin Protein
  • Axin1 protein, mouse
  • Bub1b protein, mouse
  • Cell Cycle Proteins
  • RNA, Small Interfering
  • TUBG1 protein, mouse
  • Tubulin
  • NIMA-Related Kinases
  • Nek9 protein, mouse
  • Protein Serine-Threonine Kinases

Grants and funding

This work was supported by the Medical Innovation Foundation of Fujian Province of P. R. China (No. 2009-cxb-66), the Natural Science Foundation of Fujian Province of China (No. 2012J05068), the Fundamental Research Funds for the Central Universities (No. 20720150055) and the National Natural Science Foundation of P. R. China (No. 31201695).