Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: van Biljon, Riëtte, van Wyk, Roelof, Painter, Heather J., Orchard, Lindsey, Reader, Janette, Niemand, Jandeli, Llinás, Manuel, Birkholtz, Lyn-Marie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
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
_version_ 1783475417968017408
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
work_keys_str_mv AT vanbiljonriette hierarchicaltranscriptionalcontrolregulatesplasmodiumfalciparumsexualdifferentiation
AT vanwykroelof hierarchicaltranscriptionalcontrolregulatesplasmodiumfalciparumsexualdifferentiation
AT painterheatherj hierarchicaltranscriptionalcontrolregulatesplasmodiumfalciparumsexualdifferentiation
AT orchardlindsey hierarchicaltranscriptionalcontrolregulatesplasmodiumfalciparumsexualdifferentiation
AT readerjanette hierarchicaltranscriptionalcontrolregulatesplasmodiumfalciparumsexualdifferentiation
AT niemandjandeli hierarchicaltranscriptionalcontrolregulatesplasmodiumfalciparumsexualdifferentiation
AT llinasmanuel hierarchicaltranscriptionalcontrolregulatesplasmodiumfalciparumsexualdifferentiation
AT birkholtzlynmarie hierarchicaltranscriptionalcontrolregulatesplasmodiumfalciparumsexualdifferentiation