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Spindle architecture constrains karyotype in budding yeast.

Jana HelsenMd Hashim RezaGavin SherlockGautam Dey
Published in: bioRxiv : the preprint server for biology (2023)
The eukaryotic cell division machinery must rapidly and reproducibly duplicate and partition the cell's chromosomes in a carefully coordinated process. However, chromosome number varies dramatically between genomes, even on short evolutionary timescales. We sought to understand how the mitotic machinery senses and responds to karyotypic changes by using a set of budding yeast strains in which the native chromosomes have been successively fused. Using a combination of cell biological profiling, genetic engineering, and experimental evolution, we show that chromosome fusions are well tolerated up until a critical point. However, with fewer than five centromeres, outward forces in the metaphase spindle cannot be countered by kinetochore-microtubule attachments, triggering mitotic defects. Our findings demonstrate that spindle architecture is a constraining factor for karyotype evolution.
Keyphrases
  • single cell
  • cell therapy
  • copy number
  • cell cycle
  • genome wide
  • escherichia coli
  • saccharomyces cerevisiae
  • cell proliferation
  • bone marrow