| Literature DB >> 23837920 |
Anne Aubusson-Fleury1, Geneviève Bricheux, Raghida Damaj, Michel Lemullois, Gérard Coffe, Florence Donnadieu, France Koll, Bernard Viguès, Philippe Bouchard.
Abstract
In ciliates, basal bodies and associated appendages are bound to a submembrane cytoskeleton. In Paramecium, this cytoskeleton takes the form of a thin dense layer, the epiplasm, segmented into regular territories, the units where basal bodies are inserted. Epiplasmins, the main component of the epiplasm, constitute a large family of 51 proteins distributed in 5 phylogenetic groups, each characterized by a specific molecular design. By GFP-tagging, we analyzed their differential localisation and role in epiplasm building and demonstrated that: 1) The epiplasmins display a low turnover, in agreement with the maintenance of an epiplasm layer throughout the cell cycle; 2) Regionalisation of proteins from different groups allows us to define rim, core, ring and basal body epiplasmins in the interphase cell; 3) Their dynamics allows definition of early and late epiplasmins, detected early versus late in the duplication process of the units. Epiplasmins from each group exhibit a specific combination of properties. Core and rim epiplasmins are required to build a unit; ring and basal body epiplasmins seem more dispensable, suggesting that they are not required for basal body docking. We propose a model of epiplasm unit assembly highlighting its implication in structural heredity in agreement with the evolutionary history of epiplasmins.Keywords: Basal body docking; cell morphogenesis; ciliates.; ciliogenesis; structural heredity; transition zone
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Year: 2013 PMID: 23837920 DOI: 10.1016/j.protis.2013.04.003
Source DB: PubMed Journal: Protist ISSN: 1434-4610