| Literature DB >> 27112295 |
Sihem Zitouni1, Maria E Francia2, Filipe Leal3, Susana Montenegro Gouveia3, Catarina Nabais3, Paulo Duarte3, Samuel Gilberto3, Daniela Brito3, Tyler Moyer4, Steffi Kandels-Lewis5, Midori Ohta6, Daiju Kitagawa6, Andrew J Holland4, Eric Karsenti7, Thierry Lorca8, Mariana Lince-Faria3, Mónica Bettencourt-Dias9.
Abstract
Centrioles are essential for the assembly of both centrosomes and cilia. Centriole biogenesis occurs once and only once per cell cycle and is temporally coordinated with cell-cycle progression, ensuring the formation of the right number of centrioles at the right time. The formation of new daughter centrioles is guided by a pre-existing, mother centriole. The proximity between mother and daughter centrioles was proposed to restrict new centriole formation until they separate beyond a critical distance. Paradoxically, mother and daughter centrioles overcome this distance in early mitosis, at a time when triggers for centriole biogenesis Polo-like kinase 4 (PLK4) and its substrate STIL are abundant. Here we show that in mitosis, the mitotic kinase CDK1-CyclinB binds STIL and prevents formation of the PLK4-STIL complex and STIL phosphorylation by PLK4, thus inhibiting untimely onset of centriole biogenesis. After CDK1-CyclinB inactivation upon mitotic exit, PLK4 can bind and phosphorylate STIL in G1, allowing pro-centriole assembly in the subsequent S phase. Our work shows that complementary mechanisms, such as mother-daughter centriole proximity and CDK1-CyclinB interaction with centriolar components, ensure that centriole biogenesis occurs once and only once per cell cycle, raising parallels to the cell-cycle regulation of DNA replication and centromere formation.Entities:
Keywords: CDK; PLK4; STIL; centriole duplication; centrosome; licensing; mitosis
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Year: 2016 PMID: 27112295 PMCID: PMC4867225 DOI: 10.1016/j.cub.2016.03.055
Source DB: PubMed Journal: Curr Biol ISSN: 0960-9822 Impact factor: 10.834