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Redistribution of FLAgellar Member 8 during the trypanosome life cycle: Consequences for cell fate prediction
The single flagellum of African trypanosomes is essential in multiple aspects of the parasites' development. The FLAgellar Member 8 protein (FLAM8), localised to the tip of the flagellum in cultured insect forms of Trypanosoma brucei, was identified as a marker of the locking event that control...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8459223/ https://www.ncbi.nlm.nih.gov/pubmed/33896083 http://dx.doi.org/10.1111/cmi.13347 |
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author | Calvo‐Álvarez, Estefanía Bonnefoy, Serge Salles, Audrey Benson, Fiona E. McKean, Paul G. Bastin, Philippe Rotureau, Brice |
author_facet | Calvo‐Álvarez, Estefanía Bonnefoy, Serge Salles, Audrey Benson, Fiona E. McKean, Paul G. Bastin, Philippe Rotureau, Brice |
author_sort | Calvo‐Álvarez, Estefanía |
collection | PubMed |
description | The single flagellum of African trypanosomes is essential in multiple aspects of the parasites' development. The FLAgellar Member 8 protein (FLAM8), localised to the tip of the flagellum in cultured insect forms of Trypanosoma brucei, was identified as a marker of the locking event that controls flagellum length. Here, we investigated whether FLAM8 could also reflect the flagellum maturation state in other parasite cycle stages. We observed that FLAM8 distribution extended along the entire flagellar cytoskeleton in mammalian‐infective forms. Then, a rapid FLAM8 concentration to the distal tip occurs during differentiation into early insect forms, illustrating the remodelling of an existing flagellum. In the tsetse cardia, FLAM8 further localises to the entire length of the new flagellum during an asymmetric division. Strikingly, in parasites dividing in the tsetse midgut and in the salivary glands, the amount and distribution of FLAM8 in the new flagellum were seen to predict the daughter cell fate. We propose and discuss how FLAM8 could be considered a meta‐marker of the flagellum stage and maturation state in trypanosomes. |
format | Online Article Text |
id | pubmed-8459223 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley & Sons, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-84592232021-09-28 Redistribution of FLAgellar Member 8 during the trypanosome life cycle: Consequences for cell fate prediction Calvo‐Álvarez, Estefanía Bonnefoy, Serge Salles, Audrey Benson, Fiona E. McKean, Paul G. Bastin, Philippe Rotureau, Brice Cell Microbiol Research Articles The single flagellum of African trypanosomes is essential in multiple aspects of the parasites' development. The FLAgellar Member 8 protein (FLAM8), localised to the tip of the flagellum in cultured insect forms of Trypanosoma brucei, was identified as a marker of the locking event that controls flagellum length. Here, we investigated whether FLAM8 could also reflect the flagellum maturation state in other parasite cycle stages. We observed that FLAM8 distribution extended along the entire flagellar cytoskeleton in mammalian‐infective forms. Then, a rapid FLAM8 concentration to the distal tip occurs during differentiation into early insect forms, illustrating the remodelling of an existing flagellum. In the tsetse cardia, FLAM8 further localises to the entire length of the new flagellum during an asymmetric division. Strikingly, in parasites dividing in the tsetse midgut and in the salivary glands, the amount and distribution of FLAM8 in the new flagellum were seen to predict the daughter cell fate. We propose and discuss how FLAM8 could be considered a meta‐marker of the flagellum stage and maturation state in trypanosomes. John Wiley & Sons, Inc. 2021-05-14 2021-09 /pmc/articles/PMC8459223/ /pubmed/33896083 http://dx.doi.org/10.1111/cmi.13347 Text en © 2021 Instuit Pasteur. Cellular Microbiology published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Research Articles Calvo‐Álvarez, Estefanía Bonnefoy, Serge Salles, Audrey Benson, Fiona E. McKean, Paul G. Bastin, Philippe Rotureau, Brice Redistribution of FLAgellar Member 8 during the trypanosome life cycle: Consequences for cell fate prediction |
title | Redistribution of FLAgellar Member 8 during the trypanosome life cycle: Consequences for cell fate prediction |
title_full | Redistribution of FLAgellar Member 8 during the trypanosome life cycle: Consequences for cell fate prediction |
title_fullStr | Redistribution of FLAgellar Member 8 during the trypanosome life cycle: Consequences for cell fate prediction |
title_full_unstemmed | Redistribution of FLAgellar Member 8 during the trypanosome life cycle: Consequences for cell fate prediction |
title_short | Redistribution of FLAgellar Member 8 during the trypanosome life cycle: Consequences for cell fate prediction |
title_sort | redistribution of flagellar member 8 during the trypanosome life cycle: consequences for cell fate prediction |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8459223/ https://www.ncbi.nlm.nih.gov/pubmed/33896083 http://dx.doi.org/10.1111/cmi.13347 |
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