Cep57 and Cep57L1 maintain centriole engagement in interphase to ensure centriole duplication cycle

Author:

Ito Kei K.1,Watanabe Koki1,Ishida Haruki1,Matsuhashi Kyohei1,Chinen Takumi1,Hata Shoji1,Kitagawa Daiju1ORCID

Affiliation:

1. Department of Physiological Chemistry, Graduate School of Pharmaceutical Sciences, The University of Tokyo, Bunkyo, Tokyo, Japan

Abstract

Centrioles duplicate in interphase only once per cell cycle. Newly formed centrioles remain associated with their mother centrioles. The two centrioles disengage at the end of mitosis, which licenses centriole duplication in the next cell cycle. Therefore, timely centriole disengagement is critical for the proper centriole duplication cycle. However, the mechanisms underlying centriole engagement during interphase are poorly understood. Here, we show that Cep57 and Cep57L1 cooperatively maintain centriole engagement during interphase. Codepletion of Cep57 and Cep57L1 induces precocious centriole disengagement in interphase without compromising cell cycle progression. The disengaged daughter centrioles convert into centrosomes during interphase in a Plk1-dependent manner. Furthermore, the centrioles reduplicate and the centriole number increases, which results in chromosome segregation errors. Overall, these findings demonstrate that the maintenance of centriole engagement by Cep57 and Cep57L1 during interphase is crucial for the tight control of centriole copy number and thus for proper chromosome segregation.

Funder

Ministry of Education, Culture, Sports, Science and Technology

Takeda Science Foundation

Japan Science Society

Daiichi Sankyo Foundation of Life Science

Publisher

Rockefeller University Press

Subject

Cell Biology

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