Sister kinetochore splitting and precocious disintegration of bivalents could explain the maternal age effect

  1. Agata P Zielinska
  2. Zuzana Holubcova
  3. Martyn Blayney
  4. Kay Elder
  5. Melina Schuh  Is a corresponding author
  1. Medical Research Council, United Kingdom
  2. Bourn Hall Clinic, United Kingdom

Abstract

Aneuploidy in human eggs is the leading cause of pregnancy loss and Down's syndrome. Aneuploid eggs result from chromosome segregation errors when an egg develops from a progenitor cell, called an oocyte. The mechanisms that lead to an increase in aneuploidy with advanced maternal age are largely unclear. Here, we show that many sister kinetochores in human oocytes are separated and do not behave as a single functional unit during the first meiotic division. Having separated sister kinetochores allowed bivalents to rotate by 90 degrees on the spindle and increased the risk of merotelic kinetochore-microtubule attachments. Advanced maternal age led to an increase in sister kinetochore separation, rotated bivalents and merotelic attachments. Chromosome arm cohesion was weakened, and the fraction of bivalents that precociously dissociated into univalents was increased. Together, our data reveal multiple age-related changes in chromosome architecture that could explain why oocyte aneuploidy increases with advanced maternal age.

Article and author information

Author details

  1. Agata P Zielinska

    Laboratory of Molecular Biology, Medical Research Council, Cambridge, United Kingdom
    Competing interests
    The authors declare that no competing interests exist.
  2. Zuzana Holubcova

    Laboratory of Molecular Biology, Medical Research Council, Cambridge, United Kingdom
    Competing interests
    The authors declare that no competing interests exist.
  3. Martyn Blayney

    Bourn Hall Clinic, Cambridge, United Kingdom
    Competing interests
    The authors declare that no competing interests exist.
  4. Kay Elder

    Bourn Hall Clinic, Cambridge, United Kingdom
    Competing interests
    The authors declare that no competing interests exist.
  5. Melina Schuh

    Laboratory of Molecular Biology, Medical Research Council, Cambridge, United Kingdom
    For correspondence
    mschuh@mrc-lmb.cam.ac.uk
    Competing interests
    The authors declare that no competing interests exist.

Reviewing Editor

  1. Andrea Musacchio, Max Planck Institute of Molecular Physiology, Germany

Ethics

Human subjects: The use of immature unfertilized human oocytes in this study has been approved by the UK's National Research Ethics Service under the REC reference 11/EE/0346; IRAS Project ID 84952. Immature unfertilized oocytes were donated by women receiving assisted reproduction treatment at Bourn Hall Clinic (Cambridge, UK).

Version history

  1. Received: September 4, 2015
  2. Accepted: December 9, 2015
  3. Accepted Manuscript published: December 15, 2015 (version 1)
  4. Accepted Manuscript updated: December 16, 2015 (version 2)
  5. Version of Record published: February 2, 2016 (version 3)

Copyright

© 2015, Zielinska et al.

This article is distributed under the terms of the Creative Commons Attribution License permitting unrestricted use and redistribution provided that the original author and source are credited.

Metrics

  • 4,253
    views
  • 976
    downloads
  • 102
    citations

Views, downloads and citations are aggregated across all versions of this paper published by eLife.

Download links

A two-part list of links to download the article, or parts of the article, in various formats.

Downloads (link to download the article as PDF)

Open citations (links to open the citations from this article in various online reference manager services)

Cite this article (links to download the citations from this article in formats compatible with various reference manager tools)

  1. Agata P Zielinska
  2. Zuzana Holubcova
  3. Martyn Blayney
  4. Kay Elder
  5. Melina Schuh
(2015)
Sister kinetochore splitting and precocious disintegration of bivalents could explain the maternal age effect
eLife 4:e11389.
https://doi.org/10.7554/eLife.11389

Share this article

https://doi.org/10.7554/eLife.11389

Further reading

    1. Cell Biology
    Jun Yang, Shitian Zou ... Xiaochun Bai
    Research Article

    Quiescence (G0) maintenance and exit are crucial for tissue homeostasis and regeneration in mammals. Here, we show that methyl-CpG binding protein 2 (Mecp2) expression is cell cycle-dependent and negatively regulates quiescence exit in cultured cells and in an injury-induced liver regeneration mouse model. Specifically, acute reduction of Mecp2 is required for efficient quiescence exit as deletion of Mecp2 accelerates, while overexpression of Mecp2 delays quiescence exit, and forced expression of Mecp2 after Mecp2 conditional knockout rescues cell cycle reentry. The E3 ligase Nedd4 mediates the ubiquitination and degradation of Mecp2, and thus facilitates quiescence exit. A genome-wide study uncovered the dual role of Mecp2 in preventing quiescence exit by transcriptionally activating metabolic genes while repressing proliferation-associated genes. Particularly disruption of two nuclear receptors, Rara or Nr1h3, accelerates quiescence exit, mimicking the Mecp2 depletion phenotype. Our studies unravel a previously unrecognized role for Mecp2 as an essential regulator of quiescence exit and tissue regeneration.

    1. Cancer Biology
    2. Cell Biology
    Stefanie Schmieder
    Insight

    Mutations in the gene for β-catenin cause liver cancer cells to release fewer exosomes, which reduces the number of immune cells infiltrating the tumor.