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CDK1 Prevents Unscheduled PLK4-STIL Complex Assembly in Centriole Biogenesis.
- Source :
-
Current biology : CB [Curr Biol] 2016 May 09; Vol. 26 (9), pp. 1127-37. Date of Electronic Publication: 2016 Apr 21. - Publication Year :
- 2016
-
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.<br /> (Copyright © 2016 Elsevier Ltd. All rights reserved.)
- Subjects :
- Animals
CDC2 Protein Kinase genetics
Cell Cycle physiology
Cloning, Molecular
Gene Expression Regulation, Enzymologic physiology
HeLa Cells
Humans
Intracellular Signaling Peptides and Proteins genetics
Protein Serine-Threonine Kinases genetics
Xenopus
CDC2 Protein Kinase metabolism
Centrioles physiology
Intracellular Signaling Peptides and Proteins metabolism
Protein Serine-Threonine Kinases metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1879-0445
- Volume :
- 26
- Issue :
- 9
- Database :
- MEDLINE
- Journal :
- Current biology : CB
- Publication Type :
- Academic Journal
- Accession number :
- 27112295
- Full Text :
- https://doi.org/10.1016/j.cub.2016.03.055