ALADIN is required for the production of fertile mouse oocytes

Author:

Carvalhal Sara1,Stevense Michelle2,Koehler Katrin3,Naumann Ronald4,Huebner Angela3,Jessberger Rolf2,Griffis Eric R.1

Affiliation:

1. Centre for Gene Regulation and Expression, School of Life Sciences, University of Dundee, Dundee DD1 5EH, United Kingdom

2. Institute of Physiological Chemistry, Medical Faculty Carl Gustav Carus, Technische Universität Dresden, 01307 Dresden, Germany

3. Department of Paediatrics, University Hospital Carl Gustav Carus, Technische Universität Dresden, 01307 Dresden, Germany

4. Max Planck Institute of Molecular Cell Biology and Genetics, 01307 Dresden, Germany

Abstract

Asymmetric cell divisions depend on the precise placement of the spindle apparatus. In mammalian oocytes, spindles assemble close to the cell’s center, but chromosome segregation takes place at the cell periphery where half of the chromosomes are expelled into small, nondeveloping polar bodies at anaphase. By dividing so asymmetrically, most of the cytoplasmic content within the oocyte is preserved, which is critical for successful fertilization and early development. Recently we determined that the nucleoporin ALADIN participates in spindle assembly in somatic cells, and we have also shown that female mice homozygously null for ALADIN are sterile. In this study we show that this protein is involved in specific meiotic stages, including meiotic resumption, spindle assembly, and spindle positioning. In the absence of ALADIN, polar body extrusion is compromised due to problems in spindle orientation and anchoring at the first meiotic anaphase. ALADIN null oocytes that mature far enough to be fertilized in vitro are unable to support embryonic development beyond the two-cell stage. Overall, we find that ALADIN is critical for oocyte maturation and appears to be far more essential for this process than for somatic cell divisions.

Publisher

American Society for Cell Biology (ASCB)

Subject

Cell Biology,Molecular Biology

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