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PCNT is critical for the association and conversion of centrioles to centrosomes during mitosis.
Kim, Jaeyoun; Kim, Jeongjin; Rhee, Kunsoo.
Affiliation
  • Kim J; Department of Biological Sciences, Seoul National University, Seoul 08826, Korea.
  • Kim J; Department of Biological Sciences, Seoul National University, Seoul 08826, Korea.
  • Rhee K; Department of Biological Sciences, Seoul National University, Seoul 08826, Korea rheek@snu.ac.kr.
J Cell Sci ; 132(6)2019 03 26.
Article in En | MEDLINE | ID: mdl-30814333
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.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Centrioles / Centrosome / Mitosis / Antigens Type of study: Risk_factors_studies Limits: Humans Language: En Journal: J Cell Sci Year: 2019 Type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Centrioles / Centrosome / Mitosis / Antigens Type of study: Risk_factors_studies Limits: Humans Language: En Journal: J Cell Sci Year: 2019 Type: Article