Prolonged overexpression of PLK4 leads to formation of centriole rosette clusters that are connected via canonical centrosome linker proteins

• Published in: Scientific reports 2024-02, Vol.14 (1), p.4370-4370, Article 4370
• Main Authors: Ozcan, Selahattin Can, Kalkan, Batuhan Mert, Cicek, Enes, Canbaz, Ata Alpay, Acilan, Ceyda
• Format: Article
• Language: English
• Subjects: 631/80/128/1383; 631/80/128/1965; 631/80/2373/2238; 631/80/641/1655; 631/80/641/1656; Animals; Cell cycle; Cell Cycle Proteins - metabolism; Centrioles; Centrioles - metabolism; Centrosomal Associated Proteins; Centrosome - metabolism; Centrosome amplification; Centrosome linkers; Centrosomes; Humanities and Social Sciences; Humans; Mammals - metabolism; multidisciplinary; Neoplasms - metabolism; PLK4; Progenitor cells; Protein Serine-Threonine Kinases - metabolism; Proteins; Science; Science (multidisciplinary)
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-024-53985-2

Centrosome amplification is a hallmark of cancer and PLK4 is one of the responsible factors for cancer associated centrosome amplification. Increased PLK4 levels was also shown to contribute to generation of cells with centriole amplification in mammalian tissues as olfactory neuron progenitor cells. PLK4 overexpression generates centriole rosette (CR) structures which harbor more than two centrioles each. Long term PLK4 overexpression results with centrosome amplification, but the maturation of amplified centrioles in CRs and linking of PLK4 induced amplified centrosomes has not yet been investigated in detail. Here, we show evidence for generation of large clustered centrosomes which have more than 2 centriole rosettes and define these structures as centriole rosette clusters (CRCs) in cells that have high PLK4 levels for 2 consecutive cell cycles. In addition, we show that PLK4 induced CRs follow normal centrosomal maturation processes and generate CRC structures that are inter-connected with canonical centrosomal linker proteins as C-Nap1, Rootletin and Cep68 in the second cell cycle after PLK4 induction. Increased PLK4 levels in cells with C-Nap1 and Rootletin knock-out resulted with distanced CRs and CRCs in interphase, while Nek2 knock-out inhibited separation of CRCs in prometaphase, providing functional evidence for the binding of CRC structures with centrosomal linker proteins. Taken together, these results suggest a cell cycle dependent model for PLK4 induced centrosome amplification which occurs in 2 consecutive cell cycles: (i) CR state in the first cell cycle, and (ii) CRC state in the second cell cycle.