Bidirectional intraflagellar transport is restricted to two sets of microtubule doublets in the trypanosome flagellum

Author:

Bertiaux Eloïse12,Mallet Adeline123,Fort Cécile12,Blisnick Thierry1,Bonnefoy Serge1,Jung Jamin1,Lemos Moara1,Marco Sergio45,Vaughan Sue6,Trépout Sylvain45,Tinevez Jean-Yves78ORCID,Bastin Philippe1ORCID

Affiliation:

1. Trypanosome Cell Biology Unit, INSERM U1201, Institut Pasteur, Paris, France

2. Université Pierre et Marie Curie Paris 6, Cellule Pasteur, Paris, France

3. UtechS Ultrastructural Bioimaging (Ultrapole), Institut Pasteur, Paris, France

4. Université Paris Sud, Université Paris-Saclay, Centre National de la Recherche Scientifique, UMR 9187, Orsay, France

5. Institut Curie, Paris Sciences et Lettres Research University, INSERM U1196, Orsay, France

6. Department of Biological and Medical Sciences, Faculty of Health and Life Science, Oxford Brookes University, Oxford, UK

7. UtechS Photonic Bioimaging (Imagopole), Institut Pasteur, Paris, France

8. Image Analysis Hub, Institut Pasteur, Paris, France

Abstract

Intraflagellar transport (IFT) is the rapid bidirectional movement of large protein complexes driven by kinesin and dynein motors along microtubule doublets of cilia and flagella. In this study, we used a combination of high-resolution electron and light microscopy to investigate how and where these IFT trains move within the flagellum of the protist Trypanosoma brucei. Focused ion beam scanning electron microscopy (FIB-SEM) analysis of trypanosomes showed that trains are found almost exclusively along two sets of doublets (3–4 and 7–8) and distribute in two categories according to their length. High-resolution live imaging of cells expressing mNeonGreen::IFT81 or GFP::IFT52 revealed for the first time IFT trafficking on two parallel lines within the flagellum. Anterograde and retrograde IFT occurs on each of these lines. At the distal end, a large individual anterograde IFT train is converted in several smaller retrograde trains in the space of 3–4 s while remaining on the same side of the axoneme.

Funder

Howard Hughes Medical Institute

Gordon and Betty Moore Foundation

French National Ministry for Research and Technology

La Fondation pour la Recherche Médicale

Agence Nationale de la Recherche

Investissement d’Avenir

Investissements d’Avenir

DIM-Malinf

Région Ile-de-France

Centre d’Innovation et Recherche Technologique

Institut Pasteur

Publisher

Rockefeller University Press

Subject

Cell Biology

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