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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society
2018
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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. |
format | Online Article Text |
id | pubmed-6282073 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | The Royal Society |
record_format | MEDLINE/PubMed |
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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