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The PfAlba1 RNA-binding protein is an important regulator of translational timing in Plasmodium falciparum blood stages

BACKGROUND: Transcriptome-wide ribosome occupancy studies have suggested that during the intra-erythrocytic lifecycle of Plasmodium falciparum, select mRNAs are post-transcriptionally regulated. A subset of these encodes parasite virulence factors required for invading host erythrocytes, and are cur...

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Autores principales: Vembar, Shruthi Sridhar, Macpherson, Cameron Ross, Sismeiro, Odile, Coppée, Jean-Yves, Scherf, Artur
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4587749/
https://www.ncbi.nlm.nih.gov/pubmed/26415947
http://dx.doi.org/10.1186/s13059-015-0771-5
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author Vembar, Shruthi Sridhar
Macpherson, Cameron Ross
Sismeiro, Odile
Coppée, Jean-Yves
Scherf, Artur
author_facet Vembar, Shruthi Sridhar
Macpherson, Cameron Ross
Sismeiro, Odile
Coppée, Jean-Yves
Scherf, Artur
author_sort Vembar, Shruthi Sridhar
collection PubMed
description BACKGROUND: Transcriptome-wide ribosome occupancy studies have suggested that during the intra-erythrocytic lifecycle of Plasmodium falciparum, select mRNAs are post-transcriptionally regulated. A subset of these encodes parasite virulence factors required for invading host erythrocytes, and are currently being developed as vaccine candidates. However, the molecular mechanisms that govern post-transcriptional regulation are currently unknown. RESULTS: We explore the previously identified DNA/RNA-binding protein PfAlba1, which localizes to multiple foci in the cytoplasm of P. falciparum trophozoites. We establish that PfAlba1 is essential for asexual proliferation, and subsequently investigate parasites overexpressing epitope-tagged PfAlba1 to identify its RNA targets and effects on mRNA homeostasis and translational regulation. Using deep sequencing of affinity-purified PfAlba1-associated RNAs, we identify 1193 transcripts that directly bind to PfAlba1 in trophozoites. For 105 such transcripts, 43 % of which are uncharacterized and 13 % of which encode erythrocyte invasion components, the steady state levels significantly change at this stage, evidencing a role for PfAlba1 in maintaining mRNA homeostasis. Additionally, we discover that binding of PfAlba1 to four erythrocyte invasion mRNAs, Rap1, RhopH3, CDPK1, and AMA1, is linked to translation repression in trophozoites whereas release of these mRNAs from a PfAlba1 complex in mature stages correlates with protein synthesis. CONCLUSIONS: We show that PfAlba1 binds to a sub-population of asexual stage mRNAs and fine-tunes the timing of translation. This mode of post-transcriptional regulation may be especially important for P. falciparum erythrocyte invasion components that have to be assembled into apical secretory organelles in a highly time-dependent manner towards the end of the parasite’s asexual lifecycle. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13059-015-0771-5) contains supplementary material, which is available to authorized users.
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spelling pubmed-45877492015-09-30 The PfAlba1 RNA-binding protein is an important regulator of translational timing in Plasmodium falciparum blood stages Vembar, Shruthi Sridhar Macpherson, Cameron Ross Sismeiro, Odile Coppée, Jean-Yves Scherf, Artur Genome Biol Research BACKGROUND: Transcriptome-wide ribosome occupancy studies have suggested that during the intra-erythrocytic lifecycle of Plasmodium falciparum, select mRNAs are post-transcriptionally regulated. A subset of these encodes parasite virulence factors required for invading host erythrocytes, and are currently being developed as vaccine candidates. However, the molecular mechanisms that govern post-transcriptional regulation are currently unknown. RESULTS: We explore the previously identified DNA/RNA-binding protein PfAlba1, which localizes to multiple foci in the cytoplasm of P. falciparum trophozoites. We establish that PfAlba1 is essential for asexual proliferation, and subsequently investigate parasites overexpressing epitope-tagged PfAlba1 to identify its RNA targets and effects on mRNA homeostasis and translational regulation. Using deep sequencing of affinity-purified PfAlba1-associated RNAs, we identify 1193 transcripts that directly bind to PfAlba1 in trophozoites. For 105 such transcripts, 43 % of which are uncharacterized and 13 % of which encode erythrocyte invasion components, the steady state levels significantly change at this stage, evidencing a role for PfAlba1 in maintaining mRNA homeostasis. Additionally, we discover that binding of PfAlba1 to four erythrocyte invasion mRNAs, Rap1, RhopH3, CDPK1, and AMA1, is linked to translation repression in trophozoites whereas release of these mRNAs from a PfAlba1 complex in mature stages correlates with protein synthesis. CONCLUSIONS: We show that PfAlba1 binds to a sub-population of asexual stage mRNAs and fine-tunes the timing of translation. This mode of post-transcriptional regulation may be especially important for P. falciparum erythrocyte invasion components that have to be assembled into apical secretory organelles in a highly time-dependent manner towards the end of the parasite’s asexual lifecycle. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13059-015-0771-5) contains supplementary material, which is available to authorized users. BioMed Central 2015-09-28 2015 /pmc/articles/PMC4587749/ /pubmed/26415947 http://dx.doi.org/10.1186/s13059-015-0771-5 Text en © Vembar et al. 2015 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
Vembar, Shruthi Sridhar
Macpherson, Cameron Ross
Sismeiro, Odile
Coppée, Jean-Yves
Scherf, Artur
The PfAlba1 RNA-binding protein is an important regulator of translational timing in Plasmodium falciparum blood stages
title The PfAlba1 RNA-binding protein is an important regulator of translational timing in Plasmodium falciparum blood stages
title_full The PfAlba1 RNA-binding protein is an important regulator of translational timing in Plasmodium falciparum blood stages
title_fullStr The PfAlba1 RNA-binding protein is an important regulator of translational timing in Plasmodium falciparum blood stages
title_full_unstemmed The PfAlba1 RNA-binding protein is an important regulator of translational timing in Plasmodium falciparum blood stages
title_short The PfAlba1 RNA-binding protein is an important regulator of translational timing in Plasmodium falciparum blood stages
title_sort pfalba1 rna-binding protein is an important regulator of translational timing in plasmodium falciparum blood stages
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4587749/
https://www.ncbi.nlm.nih.gov/pubmed/26415947
http://dx.doi.org/10.1186/s13059-015-0771-5
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