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.
Skip Nav Destination
Close
Article navigation
1 March 2021
Article|
January 25 2021
Cep57 and Cep57L1 maintain centriole engagement in interphase to ensure centriole duplication cycle
Kei K. Ito
,
1
Department of Physiological Chemistry, Graduate School of Pharmaceutical Sciences, The University of Tokyo, Bunkyo, Tokyo, Japan
Search for other works by this author on:
Koki Watanabe
,
1
Department of Physiological Chemistry, Graduate School of Pharmaceutical Sciences, The University of Tokyo, Bunkyo, Tokyo, Japan
Search for other works by this author on:
Haruki Ishida
,
Haruki Ishida
1
Department of Physiological Chemistry, Graduate School of Pharmaceutical Sciences, The University of Tokyo, Bunkyo, Tokyo, Japan
Search for other works by this author on:
Kyohei Matsuhashi
,
Kyohei Matsuhashi
1
Department of Physiological Chemistry, Graduate School of Pharmaceutical Sciences, The University of Tokyo, Bunkyo, Tokyo, Japan
Search for other works by this author on:
Takumi Chinen
,
Takumi Chinen
1
Department of Physiological Chemistry, Graduate School of Pharmaceutical Sciences, The University of Tokyo, Bunkyo, Tokyo, Japan
Search for other works by this author on:
Shoji Hata
,
Shoji Hata
1
Department of Physiological Chemistry, Graduate School of Pharmaceutical Sciences, The University of Tokyo, Bunkyo, Tokyo, Japan
Search for other works by this author on:
Daiju Kitagawa
1
Department of Physiological Chemistry, Graduate School of Pharmaceutical Sciences, The University of Tokyo, Bunkyo, Tokyo, Japan
Correspondence to D. Kitagawa: dkitagawa@mol.f.u-tokyo.ac.jp
Search for other works by this author on:
Kei K. Ito
1
Department of Physiological Chemistry, Graduate School of Pharmaceutical Sciences, The University of Tokyo, Bunkyo, Tokyo, Japan
Koki Watanabe
1
Department of Physiological Chemistry, Graduate School of Pharmaceutical Sciences, The University of Tokyo, Bunkyo, Tokyo, Japan
Haruki Ishida
1
Department of Physiological Chemistry, Graduate School of Pharmaceutical Sciences, The University of Tokyo, Bunkyo, Tokyo, Japan
Kyohei Matsuhashi
1
Department of Physiological Chemistry, Graduate School of Pharmaceutical Sciences, The University of Tokyo, Bunkyo, Tokyo, Japan
Takumi Chinen
1
Department of Physiological Chemistry, Graduate School of Pharmaceutical Sciences, The University of Tokyo, Bunkyo, Tokyo, Japan
Shoji Hata
1
Department of Physiological Chemistry, Graduate School of Pharmaceutical Sciences, The University of Tokyo, Bunkyo, Tokyo, Japan
Daiju Kitagawa
1
Department of Physiological Chemistry, Graduate School of Pharmaceutical Sciences, The University of Tokyo, Bunkyo, Tokyo, Japan
Correspondence to D. Kitagawa: dkitagawa@mol.f.u-tokyo.ac.jp
*
K.K. Ito and K. Watanabe contributed equally to this work.
Received:
May 21 2020
Revision Received:
October 27 2020
Accepted:
December 15 2020
Online Issn: 1540-8140
Print Issn: 0021-9525
Funding:
Daiichi Sankyo Foundation of Life Science
(NO AWARD)
Japan Science Society
(NO AWARD)
Ministry of Education, Culture, Sports, Science and Technology
(19H05651)
Takeda Science Foundation
(NO AWARD)
© 2021 Ito et al.
2021
This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms/). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 International license, as described at https://creativecommons.org/licenses/by-nc-sa/4.0/).
J Cell Biol (2021) 220 (3): e202005153.
Article history
Received:
May 21 2020
Revision Received:
October 27 2020
Accepted:
December 15 2020
Citation
Kei K. Ito, Koki Watanabe, Haruki Ishida, Kyohei Matsuhashi, Takumi Chinen, Shoji Hata, Daiju Kitagawa; Cep57 and Cep57L1 maintain centriole engagement in interphase to ensure centriole duplication cycle. J Cell Biol 1 March 2021; 220 (3): e202005153. doi: https://doi.org/10.1083/jcb.202005153
Download citation file:
Close
Sign in
Don't already have an account? Register
Client Account
You could not be signed in. Please check your email address / username and password and try again.
Sign in via your Institution
Sign in via your Institution
509
Views
0
Citations
Advertisement
Advertisement