2015/06/04 by Zuzana Holubcová, Martyn Blayney, Kay Elder +1 · 1 citation
Biochemistry, Genetics and Molecular Biology · Medicine · #Microtubule and mitosis dynamics #Reproductive Biology and Fertility #Prenatal Screening and Diagnostics
paper · doi:10.1126/science.aaa9529
openalex publication_date 2015/06/04 · openalex created_date 2025/10/10 · openalex updated_date 2026/07/31
Aneuploidy in human eggs is the leading cause of pregnancy loss and several genetic disorders such as Down syndrome. Most aneuploidy results from chromosome segregation errors during the meiotic divisions of an oocyte, the egg's progenitor cell. The basis for particularly error-prone chromosome segregation in human oocytes is not known. We analyzed meiosis in more than 100 live human oocytes and identified an error-prone chromosome-mediated spindle assembly mechanism as a major contributor to chromosome segregation defects. Human oocytes assembled a meiotic spindle independently of either centrosomes or other microtubule organizing centers. Instead, spindle assembly was mediated by chromosomes and the small guanosine triphosphatase Ran in a process requiring ~16 hours. This unusually long spindle assembly period was marked by intrinsic spindle instability and abnormal kinetochore-microtubule attachments, which favor chromosome segregation errors and provide a possible explanation for high rates of aneuploidy in human eggs.