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Cell cycle-specific loading of condensin I is regulated by the N-terminal tail of its kleisin subunit.

Shoji TaneKeishi ShintomiKazuhisa KinoshitaYuko TsubotaMakoto M YoshidaTomoko NishiyamaTatsuya Hirano
Published in: eLife (2022)
Condensin I is a pentameric protein complex that plays an essential role in mitotic chromosome assembly in eukaryotic cells. Although it has been shown that condensin I loading is mitosis specific, it remains poorly understood how the robust cell cycle regulation of condensin I is achieved. Here, we set up a panel of in vitro assays to demonstrate that cell cycle-specific loading of condensin I is regulated by the N-terminal tail (N-tail) of its kleisin subunit CAP-H. Deletion of the N-tail accelerates condensin I loading and chromosome assembly in Xenopus egg mitotic extracts. Phosphorylation-deficient and phosphorylation-mimetic mutations in the CAP-H N-tail decelerate and accelerate condensin I loading, respectively. Remarkably, deletion of the N-tail enables condensin I to assemble mitotic chromosome-like structures even in interphase extracts. Together with other extract-free functional assays in vitro, our results uncover one of the multilayered mechanisms that ensure cell cycle-specific loading of condensin I onto chromosomes.
Keyphrases
  • cell cycle
  • cell proliferation
  • copy number
  • protein kinase
  • high throughput
  • gene expression
  • high resolution
  • oxidative stress
  • small molecule
  • mass spectrometry
  • cell free
  • protein protein