Literature DB >> 26481051

PLK4 trans-Autoactivation Controls Centriole Biogenesis in Space.

Carla A M Lopes1, Swadhin Chandra Jana1, Inês Cunha-Ferreira1, Sihem Zitouni1, Inês Bento1, Paulo Duarte1, Samuel Gilberto1, Francisco Freixo1, Adán Guerrero1, Maria Francia1, Mariana Lince-Faria1, Jorge Carneiro1, Mónica Bettencourt-Dias2.   

Abstract

Centrioles are essential for cilia and centrosome assembly. In centriole-containing cells, centrioles always form juxtaposed to pre-existing ones, motivating a century-old debate on centriole biogenesis control. Here, we show that trans-autoactivation of Polo-like kinase 4 (PLK4), the trigger of centriole biogenesis, is a critical event in the spatial control of that process. We demonstrate that centrioles promote PLK4 activation through its recruitment and local accumulation. Though centriole removal reduces the proportion of active PLK4, this is rescued by concentrating PLK4 to the peroxisome lumen. Moreover, while mild overexpression of PLK4 only triggers centriole amplification at the existing centriole, higher PLK4 levels trigger both centriolar and cytoplasmatic (de novo) biogenesis. Hence, centrioles promote their assembly locally and disfavor de novo synthesis. Similar mechanisms enforcing the local concentration and/or activity of other centriole components are likely to contribute to the spatial control of centriole biogenesis under physiological conditions.
Copyright © 2015 Elsevier Inc. All rights reserved.

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Year:  2015        PMID: 26481051     DOI: 10.1016/j.devcel.2015.09.020

Source DB:  PubMed          Journal:  Dev Cell        ISSN: 1534-5807            Impact factor:   12.270


  35 in total

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8.  Autophosphorylation-induced self-assembly and STIL-dependent reinforcement underlie Plk4's ring-to-dot localization conversion around a human centriole.

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Journal:  Cell Cycle       Date:  2020-12-15       Impact factor: 4.534

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