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Andre, J.; Harrison, S.; Towers, K.; Qi, X.; Vaughan, S.; McKean, P. G.; Ginger, Michael L. (2013)
Publisher: Company of Biologists
Languages: English
Types: Article
Subjects: QH301

Classified by OpenAIRE into

mesheuropmc: macromolecular substances
TBCCD1 is an enigmatic member of the tubulin-binding cofactor C (TBCC) family of proteins required for mother–daughter centriole linkage in the green alga Chlamydomonas reinhardtii and nucleus–centrosome–Golgi linkage in mammalian cells. Loss of these linkages has severe morphogenetic consequences, but the mechanism(s) through which TBCCD1 contributes to cell organisation is unknown. In the African sleeping sickness parasite Trypanosoma brucei a microtubule-dominant cytoskeleton dictates cell shape, influencing strongly the positioning and inheritance patterns of key intracellular organelles. Here, we show the trypanosome orthologue of TBCCD1 is found at multiple locations: centrioles, the centriole-associated Golgi ‘bi-lobe’, and the anterior end of the cell body. Loss of Trypanosoma brucei TBCCD1 results in disorganisation of the structurally complex bi-lobe architecture and loss of centriole linkage to the single unit-copy mitochondrial genome (or kinetoplast) of the parasite. We therefore identify TBCCD1 as an essential protein associated with at least two filament-based structures in the trypanosome cytoskeleton. The last common ancestor of trypanosomes, animals and green algae was arguably the last common ancestor of all eukaryotes. On the basis of our observations, and interpretation of published data, we argue for an unexpected co-option of the TBCC domain for an essential non-tubulin-related function at an early point during evolution of the eukaryotic cytoskeleton.

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