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The Modular Circuitry of Apicomplexan Cell Division Plasticity
The close-knit group of apicomplexan parasites displays a wide variety of cell division modes, which differ between parasites as well as between different life stages within a single parasite species. The beginning and endpoint of the asexual replication cycles is a ‘zoite’ harboring the defining ap...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8072463/ https://www.ncbi.nlm.nih.gov/pubmed/33912479 http://dx.doi.org/10.3389/fcimb.2021.670049 |
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author | Gubbels, Marc-Jan Coppens, Isabelle Zarringhalam, Kourosh Duraisingh, Manoj T. Engelberg, Klemens |
author_facet | Gubbels, Marc-Jan Coppens, Isabelle Zarringhalam, Kourosh Duraisingh, Manoj T. Engelberg, Klemens |
author_sort | Gubbels, Marc-Jan |
collection | PubMed |
description | The close-knit group of apicomplexan parasites displays a wide variety of cell division modes, which differ between parasites as well as between different life stages within a single parasite species. The beginning and endpoint of the asexual replication cycles is a ‘zoite’ harboring the defining apical organelles required for host cell invasion. However, the number of zoites produced per division round varies dramatically and can unfold in several different ways. This plasticity of the cell division cycle originates from a combination of hard-wired developmental programs modulated by environmental triggers. Although the environmental triggers and sensors differ between species and developmental stages, widely conserved secondary messengers mediate the signal transduction pathways. These environmental and genetic input integrate in division-mode specific chromosome organization and chromatin modifications that set the stage for each division mode. Cell cycle progression is conveyed by a smorgasbord of positively and negatively acting transcription factors, often acting in concert with epigenetic reader complexes, that can vary dramatically between species as well as division modes. A unique set of cell cycle regulators with spatially distinct localization patterns insert discrete check points which permit individual control and can uncouple general cell cycle progression from nuclear amplification. Clusters of expressed genes are grouped into four functional modules seen in all division modes: 1. mother cytoskeleton disassembly; 2. DNA replication and segregation (D&S); 3. karyokinesis; 4. zoite assembly. A plug-and-play strategy results in the variety of extant division modes. The timing of mother cytoskeleton disassembly is hard-wired at the species level for asexual division modes: it is either the first step, or it is the last step. In the former scenario zoite assembly occurs at the plasma membrane (external budding), and in the latter scenario zoites are assembled in the cytoplasm (internal budding). The number of times each other module is repeated can vary regardless of this first decision, and defines the modes of cell division: schizogony, binary fission, endodyogeny, endopolygeny. |
format | Online Article Text |
id | pubmed-8072463 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-80724632021-04-27 The Modular Circuitry of Apicomplexan Cell Division Plasticity Gubbels, Marc-Jan Coppens, Isabelle Zarringhalam, Kourosh Duraisingh, Manoj T. Engelberg, Klemens Front Cell Infect Microbiol Cellular and Infection Microbiology The close-knit group of apicomplexan parasites displays a wide variety of cell division modes, which differ between parasites as well as between different life stages within a single parasite species. The beginning and endpoint of the asexual replication cycles is a ‘zoite’ harboring the defining apical organelles required for host cell invasion. However, the number of zoites produced per division round varies dramatically and can unfold in several different ways. This plasticity of the cell division cycle originates from a combination of hard-wired developmental programs modulated by environmental triggers. Although the environmental triggers and sensors differ between species and developmental stages, widely conserved secondary messengers mediate the signal transduction pathways. These environmental and genetic input integrate in division-mode specific chromosome organization and chromatin modifications that set the stage for each division mode. Cell cycle progression is conveyed by a smorgasbord of positively and negatively acting transcription factors, often acting in concert with epigenetic reader complexes, that can vary dramatically between species as well as division modes. A unique set of cell cycle regulators with spatially distinct localization patterns insert discrete check points which permit individual control and can uncouple general cell cycle progression from nuclear amplification. Clusters of expressed genes are grouped into four functional modules seen in all division modes: 1. mother cytoskeleton disassembly; 2. DNA replication and segregation (D&S); 3. karyokinesis; 4. zoite assembly. A plug-and-play strategy results in the variety of extant division modes. The timing of mother cytoskeleton disassembly is hard-wired at the species level for asexual division modes: it is either the first step, or it is the last step. In the former scenario zoite assembly occurs at the plasma membrane (external budding), and in the latter scenario zoites are assembled in the cytoplasm (internal budding). The number of times each other module is repeated can vary regardless of this first decision, and defines the modes of cell division: schizogony, binary fission, endodyogeny, endopolygeny. Frontiers Media S.A. 2021-04-12 /pmc/articles/PMC8072463/ /pubmed/33912479 http://dx.doi.org/10.3389/fcimb.2021.670049 Text en Copyright © 2021 Gubbels, Coppens, Zarringhalam, Duraisingh and Engelberg https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Cellular and Infection Microbiology Gubbels, Marc-Jan Coppens, Isabelle Zarringhalam, Kourosh Duraisingh, Manoj T. Engelberg, Klemens The Modular Circuitry of Apicomplexan Cell Division Plasticity |
title | The Modular Circuitry of Apicomplexan Cell Division Plasticity |
title_full | The Modular Circuitry of Apicomplexan Cell Division Plasticity |
title_fullStr | The Modular Circuitry of Apicomplexan Cell Division Plasticity |
title_full_unstemmed | The Modular Circuitry of Apicomplexan Cell Division Plasticity |
title_short | The Modular Circuitry of Apicomplexan Cell Division Plasticity |
title_sort | modular circuitry of apicomplexan cell division plasticity |
topic | Cellular and Infection Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8072463/ https://www.ncbi.nlm.nih.gov/pubmed/33912479 http://dx.doi.org/10.3389/fcimb.2021.670049 |
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