Literature DB >> 30814333

PCNT is critical for the association and conversion of centrioles to centrosomes during mitosis.

Jaeyoun Kim1, Jeongjin Kim1, Kunsoo Rhee2.   

Abstract

A centrosome consists of a pair of centrioles and pericentriolar material (PCM). We manipulated expression of PCNT, a key PCM protein, and investigated roles of PCM in centriole behavior during mitosis. Deletion of PCNT had little effect on interphase centrosomes. However, centrioles in PCNT-deleted mitotic cells prematurely separated and frequently amplified, revealing that centrioles are limited within the spindle poles by PCNT during mitosis. It is known that specific cleavage of PCNT is necessary for centriole separation during mitotic exit. We observed delayed centriole separation in the G0 phase when a non-cleavable mutant form of PCNT was removed or when PCNT was artificially cleaved by TEV protease. Furthermore, a daughter centriole converts to a mother centriole only after experiencing both mitotic exit and specific PCNT cleavage. Based on these results, we propose that a centriole pair disengages upon entering mitosis but remains associated with the surrounding PCM proteins throughout mitosis. During mitotic exit, specific cleavage of PCNT induces PCM disintegration. As a result, a daughter centriole separates from the mother centriole and converts to a young mother centriole.
© 2019. Published by The Company of Biologists Ltd.

Entities:  

Keywords:  Centriole disengagement; Centriole separation; Centriole-to-centrosome conversion; Centrosome; Mitosis; Pericentrin; Pericentriolar material

Mesh:

Substances:

Year:  2019        PMID: 30814333     DOI: 10.1242/jcs.225789

Source DB:  PubMed          Journal:  J Cell Sci        ISSN: 0021-9533            Impact factor:   5.285


  6 in total

1.  Triple deletion of TP53, PCNT, and CEP215 promotes centriole amplification in the M phase.

Authors:  Gee In Jung; Kunsoo Rhee
Journal:  Cell Cycle       Date:  2021-07-08       Impact factor: 5.173

2.  Centriole and PCM cooperatively recruit CEP192 to spindle poles to promote bipolar spindle assembly.

Authors:  Takumi Chinen; Kaho Yamazaki; Kaho Hashimoto; Ken Fujii; Koki Watanabe; Yutaka Takeda; Shohei Yamamoto; Yuka Nozaki; Yuki Tsuchiya; Daisuke Takao; Daiju Kitagawa
Journal:  J Cell Biol       Date:  2021-02-01       Impact factor: 10.539

3.  Treatment of microglia with Anti-PrP monoclonal antibodies induces neuronal apoptosis in vitro.

Authors:  Utpal Kumar Adhikari; Elif Sakiz; Umma Habiba; Meena Mikhael; Matteo Senesi; Monique Antoinette David; Gilles J Guillemin; Lezanne Ooi; Tim Karl; Steven Collins; Mourad Tayebi
Journal:  Heliyon       Date:  2021-12-21

Review 4.  Generation and Fates of Supernumerary Centrioles in Dividing Cells.

Authors:  Byungho Shin; Myung Se Kim; Yejoo Lee; Gee In Jung; Kunsoo Rhee
Journal:  Mol Cells       Date:  2021-10-31       Impact factor: 5.034

5.  The APC/C targets the Cep152-Cep63 complex at the centrosome to regulate mitotic spindle assembly.

Authors:  Thomas Tischer; Jing Yang; David Barford
Journal:  J Cell Sci       Date:  2022-01-18       Impact factor: 5.285

6.  Differential turnover of Nup188 controls its levels at centrosomes and role in centriole duplication.

Authors:  Nidhi Vishnoi; Karthigeyan Dhanasekeran; Madeleine Chalfant; Ivan Surovstev; Mustafa K Khokha; C Patrick Lusk
Journal:  J Cell Biol       Date:  2020-03-02       Impact factor: 10.539

  6 in total

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