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Role for the flagellum attachment zone in Leishmania anterior cell tip morphogenesis
C. Halliday, R. Yanase, CMC. Catta-Preta, F. Moreira-Leite, J. Myskova, K. Pruzinova, P. Volf, JC. Mottram, JD. Sunter
Language English Country United States
Document type Journal Article, Research Support, Non-U.S. Gov't
Grant support
200807/Z/16/Z
Wellcome Trust - United Kingdom
104627/Z/14/Z
Wellcome Trust - United Kingdom
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- MeSH
- Cell Membrane MeSH
- Cytokinesis MeSH
- Cytoskeleton metabolism MeSH
- Flagella physiology ultrastructure MeSH
- Host-Parasite Interactions * MeSH
- Leishmania growth & development ultrastructure MeSH
- Leishmaniasis parasitology MeSH
- Morphogenesis * MeSH
- Mice, Inbred BALB C MeSH
- Mice MeSH
- Protozoan Proteins genetics metabolism MeSH
- Psychodidae parasitology MeSH
- Animals MeSH
- Check Tag
- Mice MeSH
- Female MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
The shape and form of the flagellated eukaryotic parasite Leishmania is sculpted to its ecological niches and needs to be transmitted to each generation with great fidelity. The shape of the Leishmania cell is defined by the sub-pellicular microtubule array and the positioning of the nucleus, kinetoplast and the flagellum within this array. The flagellum emerges from the anterior end of the cell body through an invagination of the cell body membrane called the flagellar pocket. Within the flagellar pocket the flagellum is laterally attached to the side of the flagellar pocket by a cytoskeletal structure called the flagellum attachment zone (FAZ). During the cell cycle single copy organelles duplicate with a new flagellum assembling alongside the old flagellum. These are then segregated between the two daughter cells by cytokinesis, which initiates at the anterior cell tip. Here, we have investigated the role of the FAZ in the morphogenesis of the anterior cell tip. We have deleted the FAZ filament protein, FAZ2 and investigated its function using light and electron microscopy and infection studies. The loss of FAZ2 caused a disruption to the membrane organisation at the anterior cell tip, resulting in cells that were connected to each other by a membranous bridge structure between their flagella. Moreover, the FAZ2 null mutant was unable to develop and proliferate in sand flies and had a reduced parasite burden in mice. Our study provides a deeper understanding of membrane-cytoskeletal interactions that define the shape and form of an individual cell and the remodelling of that form during cell division.
Department of Biological and Medical Sciences Oxford Brookes University Oxford United Kingdom
Department of Parasitology Charles University Prague Czech Republic
Shimoda Marine Research Center University of Tsukuba Shizuoka Japan
York Biomedical Research Institute and Department of Biology University of York York United Kingdom
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