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First published online 11 April 2006
doi: 10.1242/jcs.02900
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Research Article |
Laboratoire de Génomique Fonctionnelle des Trypanosomatides, CNRS UMR 5162, Université Bordeaux 2, 146 rue Léo Saignat, Bât. 3A, 33076 Bordeaux CEDEX, France
* Author for correspondence (e-mail: Derrick.Robinson{at}parasitmol.u-bordeaux2.fr)
Accepted 20 January 2006
The NIMA-related kinase 2 (NEK 2) has important cell cycle functions related to centriole integrity and splitting. Trypanosoma brucei does not possess centrioles, however, cytokinesis is coupled to basal body separation events. Here we report the first functional characterisation of a T. brucei basal body-cytoskeletal NIMA-related kinase (NRK) protein, TbNRKC. The TbNRKC kinase domain has high amino acid identity with the human NEK1 kinase domain (50%) but also shares 42% identity with human NEK2. TbNRKC is expressed in bloodstream and procyclic cells and functions as a bona fide kinase in vitro. Remarkably, RNAi knockdown of TbNRKC and overexpression of kinase-dead TbNRKC in procyclic forms induces the accumulation of cells with four basal bodies, whereas overexpression of active protein produces supernumary basal bodies and blocks cytokinesis. TbNRKC is located on mature and immature basal bodies and is the first T. brucei NRK to be found associated with the basal body cytokinesis pathway.
Key words: NEK, Basal body, Cytokinesis, T. brucei, Cell cycle
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