Inherent Instability of Correct Kinetochore-Microtubule Attachments during Meiosis I in Oocytes

Dev Cell. 2015 Jun 8;33(5):589-602. doi: 10.1016/j.devcel.2015.04.020. Epub 2015 May 28.

Abstract

A model for mitosis suggests that correct kinetochore-microtubule (KT-MT) attachments are stabilized by spatial separation of the attachment sites from Aurora B kinase through sister KT stretching. However, the spatiotemporal regulation of attachment stability during meiosis I (MI) in oocytes remains unclear. Here, we found that in mouse oocytes, Aurora B and C (B/C) are located in close proximity to KT-MT attachment sites after bivalent stretching due to an intrinsic property of the MI chromosomes. The Aurora B/C activity destabilizes correct attachments while allowing a considerable amount of incorrect attachments to form. KT-MT attachments are eventually stabilized through KT dephosphorylation by PP2A-B56 phosphatase, which is progressively recruited to KTs depending on the BubR1 phosphorylation resulting from the timer Cdk1 and independent of bivalent stretching. Thus, oocytes lack a mechanism for coordinating bivalent stretching and KT phosphoregulation during MI, which may explain the high frequency of KT-MT attachment errors.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Aurora Kinase B / metabolism
  • Aurora Kinase C / metabolism
  • CDC2 Protein Kinase / metabolism
  • Cell Cycle Proteins / metabolism
  • Chromosome Segregation*
  • Female
  • Fluorescent Antibody Technique
  • Image Processing, Computer-Assisted
  • Kinetochores / physiology*
  • Meiosis / physiology*
  • Mice
  • Microtubules / physiology*
  • Oocytes / cytology
  • Oocytes / metabolism*
  • Phosphorylation
  • Protein Phosphatase 2 / metabolism
  • Protein Serine-Threonine Kinases / metabolism

Substances

  • Bub1b protein, mouse
  • Cell Cycle Proteins
  • Aurora Kinase B
  • Aurora Kinase C
  • Bub1 spindle checkpoint protein
  • Protein Serine-Threonine Kinases
  • CDC2 Protein Kinase
  • Ppp2r5a protein, mouse
  • Protein Phosphatase 2