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Non‐equivalence in old‐ and new‐flagellum daughter cells of a proliferative division in Trypanosoma brucei
Differentiation of Trypanosoma brucei, a flagellated protozoan parasite, between life cycle stages typically occurs through an asymmetric cell division process, producing two morphologically distinct daughter cells. Conversely, proliferative cell divisions produce two daughter cells, which look simi...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6771564/ https://www.ncbi.nlm.nih.gov/pubmed/31286583 http://dx.doi.org/10.1111/mmi.14345 |
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author | Abeywickrema, Movin Vachova, Hana Farr, Helen Mohr, Timm Wheeler, Richard J. Lai, De‐Hua Vaughan, Sue Gull, Keith Sunter, Jack D. Varga, Vladimir |
author_facet | Abeywickrema, Movin Vachova, Hana Farr, Helen Mohr, Timm Wheeler, Richard J. Lai, De‐Hua Vaughan, Sue Gull, Keith Sunter, Jack D. Varga, Vladimir |
author_sort | Abeywickrema, Movin |
collection | PubMed |
description | Differentiation of Trypanosoma brucei, a flagellated protozoan parasite, between life cycle stages typically occurs through an asymmetric cell division process, producing two morphologically distinct daughter cells. Conversely, proliferative cell divisions produce two daughter cells, which look similar but are not identical. To examine in detail differences between the daughter cells of a proliferative division of procyclic T. brucei we used the recently identified constituents of the flagella connector. These segregate asymmetrically during cytokinesis allowing the new‐flagellum and the old‐flagellum daughters to be distinguished. We discovered that there are distinct morphological differences between the two daughters, with the new‐flagellum daughter in particular re‐modelling rapidly and extensively in early G1. This re‐modelling process involves an increase in cell body, flagellum and flagellum attachment zone length and is accompanied by architectural changes to the anterior cell end. The old‐flagellum daughter undergoes a different G1 re‐modelling, however, despite this there was no difference in G1 duration of their respective cell cycles. This work demonstrates that the two daughters of a proliferative division of T. brucei are non‐equivalent and enables more refined morphological analysis of mutant phenotypes. We suggest all proliferative divisions in T. brucei and related organisms will involve non‐equivalence. |
format | Online Article Text |
id | pubmed-6771564 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-67715642019-10-03 Non‐equivalence in old‐ and new‐flagellum daughter cells of a proliferative division in Trypanosoma brucei Abeywickrema, Movin Vachova, Hana Farr, Helen Mohr, Timm Wheeler, Richard J. Lai, De‐Hua Vaughan, Sue Gull, Keith Sunter, Jack D. Varga, Vladimir Mol Microbiol Research Articles Differentiation of Trypanosoma brucei, a flagellated protozoan parasite, between life cycle stages typically occurs through an asymmetric cell division process, producing two morphologically distinct daughter cells. Conversely, proliferative cell divisions produce two daughter cells, which look similar but are not identical. To examine in detail differences between the daughter cells of a proliferative division of procyclic T. brucei we used the recently identified constituents of the flagella connector. These segregate asymmetrically during cytokinesis allowing the new‐flagellum and the old‐flagellum daughters to be distinguished. We discovered that there are distinct morphological differences between the two daughters, with the new‐flagellum daughter in particular re‐modelling rapidly and extensively in early G1. This re‐modelling process involves an increase in cell body, flagellum and flagellum attachment zone length and is accompanied by architectural changes to the anterior cell end. The old‐flagellum daughter undergoes a different G1 re‐modelling, however, despite this there was no difference in G1 duration of their respective cell cycles. This work demonstrates that the two daughters of a proliferative division of T. brucei are non‐equivalent and enables more refined morphological analysis of mutant phenotypes. We suggest all proliferative divisions in T. brucei and related organisms will involve non‐equivalence. John Wiley and Sons Inc. 2019-07-25 2019-09 /pmc/articles/PMC6771564/ /pubmed/31286583 http://dx.doi.org/10.1111/mmi.14345 Text en © 2019 The Authors. Molecular Microbiology Published by John Wiley & Sons Ltd This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Abeywickrema, Movin Vachova, Hana Farr, Helen Mohr, Timm Wheeler, Richard J. Lai, De‐Hua Vaughan, Sue Gull, Keith Sunter, Jack D. Varga, Vladimir Non‐equivalence in old‐ and new‐flagellum daughter cells of a proliferative division in Trypanosoma brucei |
title | Non‐equivalence in old‐ and new‐flagellum daughter cells of a proliferative division in Trypanosoma brucei
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title_full | Non‐equivalence in old‐ and new‐flagellum daughter cells of a proliferative division in Trypanosoma brucei
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title_fullStr | Non‐equivalence in old‐ and new‐flagellum daughter cells of a proliferative division in Trypanosoma brucei
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title_full_unstemmed | Non‐equivalence in old‐ and new‐flagellum daughter cells of a proliferative division in Trypanosoma brucei
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title_short | Non‐equivalence in old‐ and new‐flagellum daughter cells of a proliferative division in Trypanosoma brucei
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title_sort | non‐equivalence in old‐ and new‐flagellum daughter cells of a proliferative division in trypanosoma brucei |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6771564/ https://www.ncbi.nlm.nih.gov/pubmed/31286583 http://dx.doi.org/10.1111/mmi.14345 |
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