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Hierarchical transcriptional control regulates Plasmodium falciparum sexual differentiation
BACKGROUND: Malaria pathogenesis relies on sexual gametocyte forms of the malaria parasite to be transmitted between the infected human and the mosquito host but the molecular mechanisms controlling gametocytogenesis remains poorly understood. Here we provide a high-resolution transcriptome of Plasm...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6889441/ https://www.ncbi.nlm.nih.gov/pubmed/31795940 http://dx.doi.org/10.1186/s12864-019-6322-9 |
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author | van Biljon, Riëtte van Wyk, Roelof Painter, Heather J. Orchard, Lindsey Reader, Janette Niemand, Jandeli Llinás, Manuel Birkholtz, Lyn-Marie |
author_facet | van Biljon, Riëtte van Wyk, Roelof Painter, Heather J. Orchard, Lindsey Reader, Janette Niemand, Jandeli Llinás, Manuel Birkholtz, Lyn-Marie |
author_sort | van Biljon, Riëtte |
collection | PubMed |
description | BACKGROUND: Malaria pathogenesis relies on sexual gametocyte forms of the malaria parasite to be transmitted between the infected human and the mosquito host but the molecular mechanisms controlling gametocytogenesis remains poorly understood. Here we provide a high-resolution transcriptome of Plasmodium falciparum as it commits to and develops through gametocytogenesis. RESULTS: The gametocyte-associated transcriptome is significantly different from that of the asexual parasites, with dynamic gene expression shifts characterizing early, intermediate and late-stage gametocyte development and results in differential timing for sex-specific transcripts. The transcriptional dynamics suggest strict transcriptional control during gametocytogenesis in P. falciparum, which we propose is mediated by putative regulators including epigenetic mechanisms (driving active repression of proliferation-associated processes) and a cascade-like expression of ApiAP2 transcription factors. CONCLUSIONS: The gametocyte transcriptome serves as the blueprint for sexual differentiation and will be a rich resource for future functional studies on this critical stage of Plasmodium development, as the intraerythrocytic transcriptome has been for our understanding of the asexual cycle. |
format | Online Article Text |
id | pubmed-6889441 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-68894412019-12-11 Hierarchical transcriptional control regulates Plasmodium falciparum sexual differentiation van Biljon, Riëtte van Wyk, Roelof Painter, Heather J. Orchard, Lindsey Reader, Janette Niemand, Jandeli Llinás, Manuel Birkholtz, Lyn-Marie BMC Genomics Research Article BACKGROUND: Malaria pathogenesis relies on sexual gametocyte forms of the malaria parasite to be transmitted between the infected human and the mosquito host but the molecular mechanisms controlling gametocytogenesis remains poorly understood. Here we provide a high-resolution transcriptome of Plasmodium falciparum as it commits to and develops through gametocytogenesis. RESULTS: The gametocyte-associated transcriptome is significantly different from that of the asexual parasites, with dynamic gene expression shifts characterizing early, intermediate and late-stage gametocyte development and results in differential timing for sex-specific transcripts. The transcriptional dynamics suggest strict transcriptional control during gametocytogenesis in P. falciparum, which we propose is mediated by putative regulators including epigenetic mechanisms (driving active repression of proliferation-associated processes) and a cascade-like expression of ApiAP2 transcription factors. CONCLUSIONS: The gametocyte transcriptome serves as the blueprint for sexual differentiation and will be a rich resource for future functional studies on this critical stage of Plasmodium development, as the intraerythrocytic transcriptome has been for our understanding of the asexual cycle. BioMed Central 2019-12-03 /pmc/articles/PMC6889441/ /pubmed/31795940 http://dx.doi.org/10.1186/s12864-019-6322-9 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article van Biljon, Riëtte van Wyk, Roelof Painter, Heather J. Orchard, Lindsey Reader, Janette Niemand, Jandeli Llinás, Manuel Birkholtz, Lyn-Marie Hierarchical transcriptional control regulates Plasmodium falciparum sexual differentiation |
title | Hierarchical transcriptional control regulates Plasmodium falciparum sexual differentiation |
title_full | Hierarchical transcriptional control regulates Plasmodium falciparum sexual differentiation |
title_fullStr | Hierarchical transcriptional control regulates Plasmodium falciparum sexual differentiation |
title_full_unstemmed | Hierarchical transcriptional control regulates Plasmodium falciparum sexual differentiation |
title_short | Hierarchical transcriptional control regulates Plasmodium falciparum sexual differentiation |
title_sort | hierarchical transcriptional control regulates plasmodium falciparum sexual differentiation |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6889441/ https://www.ncbi.nlm.nih.gov/pubmed/31795940 http://dx.doi.org/10.1186/s12864-019-6322-9 |
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