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Triple deletion of TP53, PCNT, and CEP215 promotes centriole amplification in the M phase
Cited 2 time in
Web of Science
Cited 2 time in Scopus
- Authors
- Issue Date
- 2021-08
- Publisher
- Landes Bioscience
- Citation
- Cell Cycle, Vol.20 No.15, pp.1500-1517
- Abstract
- Supernumerary centrioles are frequently observed in diverse types of cancer cells. In this study, we investigated the mechanism underlying the generation of supernumerary centrioles during the M phase. We generated the TP53;PCNT;CEP215 triple knockout (KO) cells and determined the configurations of the centriole during the cell cycle. The triple KO cells exhibited a precocious separation of centrioles and unscheduled centriole assembly in the M phase. Supernumerary centrioles in the triple KO cells were present throughout the cell cycle; however, among all the centrioles, only two maintained an intact composition, including CEP135, CEP192, CEP295 and CEP152. Intact centrioles were formed during the S phase and the rest of the centrioles may be generated during the M phase. M-phase-assembled centrioles lacked the ability to organize microtubules in the interphase; however, a fraction of them may acquire pericentriolar material to organize microtubules during the M phase. Taken together, our work reveals the heterogeneity of the supernumerary centrioles in the triple KO cells.
- ISSN
- 1538-4101
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