Centriole distal-end proteins CP110 and Cep97 influence centriole cartwheel growth at the proximal end

Author:

Aydogan Mustafa G.12ORCID,Hankins Laura E.1ORCID,Steinacker Thomas L.1ORCID,Mofatteh Mohammad1ORCID,Saurya Saroj1ORCID,Wainman Alan1ORCID,Wong Siu-Shing1ORCID,Lu Xin34,Zhou Felix Y.34ORCID,Raff Jordan W.1ORCID

Affiliation:

1. Sir William Dunn School of Pathology, University of Oxford 1 , Oxford OX1 3RE , UK

2. University of California, San Francisco 2 Department of Biochemistry and Biophysics , , San Francisco, CA 94158 , USA

3. Ludwig Institute for Cancer Research 3 , Nuffield Department of Clinical Medicine , , Oxford OX3 7DQ , UK

4. University of Oxford 3 , Nuffield Department of Clinical Medicine , , Oxford OX3 7DQ , UK

Abstract

ABSTRACT Centrioles are composed of a central cartwheel tethered to nine-fold symmetric microtubule (MT) blades. The centriole cartwheel and MTs are thought to grow from opposite ends of these organelles, so it is unclear how they coordinate their assembly. We previously showed that in Drosophila embryos an oscillation of Polo-like kinase 4 (Plk4) helps to initiate and time the growth of the cartwheel at the proximal end. Here, in the same model, we show that CP110 and Cep97 form a complex close to the distal-end of the centriole MTs whose levels rise and fall as the new centriole MTs grow, in a manner that appears to be entrained by the core cyclin-dependent kinase (Cdk)–Cyclin oscillator that drives the nuclear divisions in these embryos. These CP110 and Cep97 dynamics, however, do not appear to time the period of centriole MT growth directly. Instead, we find that changing the levels of CP110 and Cep97 appears to alter the Plk4 oscillation and the growth of the cartwheel at the proximal end. These findings reveal an unexpected potential crosstalk between factors normally concentrated at opposite ends of the growing centrioles, which might help to coordinate centriole growth. This article has an associated First Person interview with the first authors of the paper.

Funder

Wellcome Trust

Edward Penley Abraham Scholarship

Sandler Foundation

University of California, San Francisco

Ludwig Institute for Cancer Research

University of Oxford

Publisher

The Company of Biologists

Subject

Cell Biology

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