Ccdc13; a novel human centriolar satellite protein required for ciliogenesis and genome stability
Author(s) -
Christopher J. Staples,
Katie Myers,
Ryan Beveridge,
Abhijit A. Patil,
Anna E. Howard,
Giancarlo Barone,
Alvin Lee,
Charles Swanton,
Michael Howell,
Sarah Maslen,
Mark Skehel,
Simon J. Boulton,
Spencer J. Collis
Publication year - 2014
Publication title -
journal of cell science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.384
H-Index - 278
eISSN - 1477-9137
pISSN - 0021-9533
DOI - 10.1242/jcs.147785
Subject(s) - ciliogenesis , centrosome , biology , cilium , centriole , ciliopathy , microbiology and biotechnology , basal body , microtubule , ciliopathies , mitosis , genetics , gene , flagellum , phenotype , cell cycle
Here, we identify coiled-coil domain-containing protein 13 (Ccdc13) in a genome-wide RNA interference screen for regulators of genome stability. We establish that Ccdc13 is a newly identified centriolar satellite protein that interacts with PCM1, Cep290 and pericentrin and prevents the accumulation of DNA damage during mitotic transit. Depletion of Ccdc13 results in the loss of microtubule organisation in a manner similar to PCM1 and Cep290 depletion, although Ccdc13 is not required for satellite integrity. We show that microtubule regrowth is enhanced in Ccdc13-depleted cells, but slowed in cells that overexpress Ccdc13. Furthermore, in serum-starved cells, Ccdc13 localises to the basal body, is required for primary cilia formation and promotes the localisation of the ciliopathy protein BBS4 to both centriolar satellites and cilia. These data highlight the emerging link between DNA damage response factors, centriolar and peri-centriolar satellites and cilia-associated proteins and implicate Ccdc13 as a centriolar satellite protein that functions to promote both genome stability and cilia formation.
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