A Dynamic Protein Interaction Landscape of the Human Centrosome-Cilium Interface
Author(s) -
Gagan D. Gupta,
Étienne Coyaud,
João Gonçalves,
Bahareh A. Mojarad,
Yi Liu,
Qianzhu Wu,
Ladan Gheiratmand,
David Comartin,
Johnny M. Tkach,
Sally W.T. Cheung,
Mikhail Bashkurov,
Monica Hasegan,
James D.R. Knight,
ZhenYuan Lin,
Markus Schueler,
Friedhelm Hildebrandt,
Jason Moffat,
AnneClaude Gingras,
Brian Raught,
Laurence Pelletier
Publication year - 2015
Publication title -
cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 26.304
H-Index - 776
eISSN - 1097-4172
pISSN - 0092-8674
DOI - 10.1016/j.cell.2015.10.065
Subject(s) - ciliogenesis , centrosome , cilium , centriole , biology , motile cilium , microbiology and biotechnology , microtubule , basal body , ciliopathies , computational biology , phenotype , flagellum , genetics , cell , cell cycle , gene
The centrosome is the primary microtubule organizing center of the cells and templates the formation of cilia, thereby operating at a nexus of critical cellular functions. Here, we use proximity-dependent biotinylation (BioID) to map the centrosome-cilium interface; with 58 bait proteins we generate a protein topology network comprising >7,000 interactions. Analysis of interaction profiles coupled with high resolution phenotypic profiling implicates a number of protein modules in centriole duplication, ciliogenesis, and centriolar satellite biogenesis and highlights extensive interplay between these processes. By monitoring dynamic changes in the centrosome-cilium protein interaction landscape during ciliogenesis, we also identify satellite proteins that support cilia formation. Systematic profiling of proximity interactions combined with functional analysis thus provides a rich resource for better understanding human centrosome and cilia biology. Similar strategies may be applied to other complex biological structures or pathways.
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