Format

Send to

Choose Destination
J Cell Sci. 2013 Jul 15;126(Pt 14):3223-33. doi: 10.1242/jcs.129502. Epub 2013 May 2.

Human Cep192 and Cep152 cooperate in Plk4 recruitment and centriole duplication.

Author information

1
Biozentrum, University of Basel, Klingelbergstrasse 50/70, 4056 Basel, Switzerland.

Abstract

Polo-like kinase 4 (Plk4) is a key regulator of centriole duplication, but the mechanism underlying its recruitment to mammalian centrioles is not understood. In flies, Plk4 recruitment depends on Asterless, whereas nematodes rely on a distinct protein, Spd-2. Here, we have explored the roles of two homologous mammalian proteins, Cep152 and Cep192, in the centriole recruitment of human Plk4. We demonstrate that Cep192 plays a key role in centrosome recruitment of both Cep152 and Plk4. Double-depletion of Cep192 and Cep152 completely abolishes Plk4 binding to centrioles as well as centriole duplication, indicating that the two proteins cooperate. Most importantly, we show that Cep192 binds Plk4 through an N-terminal extension that is specific to the largest isoform. The Plk4 binding regions of Cep192 and Cep152 (residues 190-240 and 1-46, respectively) are rich in negatively charged amino acids, suggesting that Plk4 localization to centrioles depends on electrostatic interactions with the positively charged polo-box domain. We conclude that cooperation between Cep192 and Cep152 is crucial for centriole recruitment of Plk4 and centriole duplication during the cell cycle.

KEYWORDS:

Centriole duplication; Centrosome; Cep152; Cep192; Plk4

PMID:
23641073
DOI:
10.1242/jcs.129502
[Indexed for MEDLINE]
Free full text

Supplemental Content

Full text links

Icon for HighWire
Loading ...
Support Center