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Dependency relationships between IFT-dependent flagellum elongation and cell morphogenesis in Leishmania

Flagella have multiple functions that are associated with different axonemal structures. Motile flagella typically have a 9 + 2 arrangement of microtubules, whereas sensory flagella normally have a 9 + 0 arrangement. Leishmania exhibits both of these flagellum forms and differentiation between these...

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Autores principales: Sunter, Jack Daniel, Moreira-Leite, Flavia, Gull, Keith
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6282073/
https://www.ncbi.nlm.nih.gov/pubmed/30463910
http://dx.doi.org/10.1098/rsob.180124
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author Sunter, Jack Daniel
Moreira-Leite, Flavia
Gull, Keith
author_facet Sunter, Jack Daniel
Moreira-Leite, Flavia
Gull, Keith
author_sort Sunter, Jack Daniel
collection PubMed
description Flagella have multiple functions that are associated with different axonemal structures. Motile flagella typically have a 9 + 2 arrangement of microtubules, whereas sensory flagella normally have a 9 + 0 arrangement. Leishmania exhibits both of these flagellum forms and differentiation between these two flagellum forms is associated with cytoskeletal and cell shape changes. We disrupted flagellum elongation in Leishmania by deleting the intraflagellar transport (IFT) protein IFT140 and examined the effects on cell morphogenesis. Δift140 cells have no external flagellum, having only a very short flagellum within the flagellar pocket. This short flagellum had a collapsed 9 + 0 (9v) axoneme configuration reminiscent of that in the amastigote and was not attached to the pocket membrane. Although amastigote-like changes occurred in the flagellar cytoskeleton, the cytoskeletal structures of Δift140 cells retained their promastigote configurations, as examined by fluorescence microscopy of tagged proteins and serial electron tomography. Thus, Leishmania promastigote cell morphogenesis does not depend on the formation of a long flagellum attached at the neck. Furthermore, our data show that disruption of the IFT system is sufficient to produce a switch from the 9 + 2 to the collapsed 9 + 0 (9v) axonemal structure, echoing the process that occurs during the promastigote to amastigote differentiation.
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spelling pubmed-62820732018-12-11 Dependency relationships between IFT-dependent flagellum elongation and cell morphogenesis in Leishmania Sunter, Jack Daniel Moreira-Leite, Flavia Gull, Keith Open Biol Research Flagella have multiple functions that are associated with different axonemal structures. Motile flagella typically have a 9 + 2 arrangement of microtubules, whereas sensory flagella normally have a 9 + 0 arrangement. Leishmania exhibits both of these flagellum forms and differentiation between these two flagellum forms is associated with cytoskeletal and cell shape changes. We disrupted flagellum elongation in Leishmania by deleting the intraflagellar transport (IFT) protein IFT140 and examined the effects on cell morphogenesis. Δift140 cells have no external flagellum, having only a very short flagellum within the flagellar pocket. This short flagellum had a collapsed 9 + 0 (9v) axoneme configuration reminiscent of that in the amastigote and was not attached to the pocket membrane. Although amastigote-like changes occurred in the flagellar cytoskeleton, the cytoskeletal structures of Δift140 cells retained their promastigote configurations, as examined by fluorescence microscopy of tagged proteins and serial electron tomography. Thus, Leishmania promastigote cell morphogenesis does not depend on the formation of a long flagellum attached at the neck. Furthermore, our data show that disruption of the IFT system is sufficient to produce a switch from the 9 + 2 to the collapsed 9 + 0 (9v) axonemal structure, echoing the process that occurs during the promastigote to amastigote differentiation. The Royal Society 2018-11-21 /pmc/articles/PMC6282073/ /pubmed/30463910 http://dx.doi.org/10.1098/rsob.180124 Text en © 2018 The Authors. http://creativecommons.org/licenses/by/4.0/ Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, provided the original author and source are credited.
spellingShingle Research
Sunter, Jack Daniel
Moreira-Leite, Flavia
Gull, Keith
Dependency relationships between IFT-dependent flagellum elongation and cell morphogenesis in Leishmania
title Dependency relationships between IFT-dependent flagellum elongation and cell morphogenesis in Leishmania
title_full Dependency relationships between IFT-dependent flagellum elongation and cell morphogenesis in Leishmania
title_fullStr Dependency relationships between IFT-dependent flagellum elongation and cell morphogenesis in Leishmania
title_full_unstemmed Dependency relationships between IFT-dependent flagellum elongation and cell morphogenesis in Leishmania
title_short Dependency relationships between IFT-dependent flagellum elongation and cell morphogenesis in Leishmania
title_sort dependency relationships between ift-dependent flagellum elongation and cell morphogenesis in leishmania
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6282073/
https://www.ncbi.nlm.nih.gov/pubmed/30463910
http://dx.doi.org/10.1098/rsob.180124
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