Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Calvo‐Álvarez, Estefanía, Bonnefoy, Serge, Salles, Audrey, Benson, Fiona E., McKean, Paul G., Bastin, Philippe, Rotureau, Brice
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2021
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
_version_ 1784571472819257344
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
work_keys_str_mv AT calvoalvarezestefania redistributionofflagellarmember8duringthetrypanosomelifecycleconsequencesforcellfateprediction
AT bonnefoyserge redistributionofflagellarmember8duringthetrypanosomelifecycleconsequencesforcellfateprediction
AT sallesaudrey redistributionofflagellarmember8duringthetrypanosomelifecycleconsequencesforcellfateprediction
AT bensonfionae redistributionofflagellarmember8duringthetrypanosomelifecycleconsequencesforcellfateprediction
AT mckeanpaulg redistributionofflagellarmember8duringthetrypanosomelifecycleconsequencesforcellfateprediction
AT bastinphilippe redistributionofflagellarmember8duringthetrypanosomelifecycleconsequencesforcellfateprediction
AT rotureaubrice redistributionofflagellarmember8duringthetrypanosomelifecycleconsequencesforcellfateprediction