Aurora kinase A is essential for meiosis in mouse oocytes

PLoS Genet. 2021 Apr 26;17(4):e1009327. doi: 10.1371/journal.pgen.1009327. eCollection 2021 Apr.

Abstract

The Aurora protein kinases are well-established regulators of spindle building and chromosome segregation in mitotic and meiotic cells. In mouse oocytes, there is significant Aurora kinase A (AURKA) compensatory abilities when the other Aurora kinase homologs are deleted. Whether the other homologs, AURKB or AURKC can compensate for loss of AURKA is not known. Using a conditional mouse oocyte knockout model, we demonstrate that this compensation is not reciprocal because female oocyte-specific knockout mice are sterile, and their oocytes fail to complete meiosis I. In determining AURKA-specific functions, we demonstrate that its first meiotic requirement is to activate Polo-like kinase 1 at acentriolar microtubule organizing centers (aMTOCs; meiotic spindle poles). This activation induces fragmentation of the aMTOCs, a step essential for building a bipolar spindle. We also show that AURKA is required for regulating localization of TACC3, another protein required for spindle building. We conclude that AURKA has multiple functions essential to completing MI that are distinct from AURKB and AURKC.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Aurora Kinase A / genetics*
  • Aurora Kinase B / genetics
  • Aurora Kinase C / genetics
  • Cell Cycle Proteins / genetics*
  • Cell Nucleus Division / genetics
  • Chromosome Segregation / genetics
  • Female
  • Fetal Proteins / genetics*
  • Gene Expression Regulation, Developmental / genetics
  • Humans
  • Meiosis / genetics*
  • Mice
  • Microtubule-Associated Proteins / genetics*
  • Microtubule-Organizing Center / metabolism
  • Oocytes / growth & development*
  • Oocytes / metabolism
  • Polo-Like Kinase 1
  • Protein Serine-Threonine Kinases / genetics*
  • Proto-Oncogene Proteins / genetics*
  • Spindle Apparatus / genetics
  • Spindle Poles / genetics

Substances

  • Cell Cycle Proteins
  • Fetal Proteins
  • Microtubule-Associated Proteins
  • Proto-Oncogene Proteins
  • TACC3 protein, mouse
  • Aurkb protein, mouse
  • Aurkc protein, mouse
  • Aurora Kinase A
  • Aurora Kinase B
  • Aurora Kinase C
  • Protein Serine-Threonine Kinases