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

Author:

Tane Shoji1ORCID,Shintomi Keishi1ORCID,Kinoshita Kazuhisa1ORCID,Tsubota Yuko2ORCID,Yoshida Makoto M1ORCID,Nishiyama Tomoko2ORCID,Hirano Tatsuya1ORCID

Affiliation:

1. Chromosome Dynamics Laboratory, RIKEN

2. Division of Biological Sciences, Graduate School of Science, Nagoya University

Abstract

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.

Funder

Japan Society for the Promotion of Science

Precursory Research for Embryonic Science and Technology

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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