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Deciphering the principles that govern mutually exclusive expression of Plasmodium falciparum clag3 genes

The product of the Plasmodium falciparum genes clag3.1 and clag3.2 plays a fundamental role in malaria parasite biology by determining solute transport into infected erythrocytes. Expression of the two clag3 genes is mutually exclusive, such that a single parasite expresses only one of the two genes...

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Autores principales: Rovira-Graells, Núria, Crowley, Valerie M., Bancells, Cristina, Mira-Martínez, Sofía, Ribas de Pouplana, Lluís, Cortés, Alfred
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4787829/
https://www.ncbi.nlm.nih.gov/pubmed/26202963
http://dx.doi.org/10.1093/nar/gkv730
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author Rovira-Graells, Núria
Crowley, Valerie M.
Bancells, Cristina
Mira-Martínez, Sofía
Ribas de Pouplana, Lluís
Cortés, Alfred
author_facet Rovira-Graells, Núria
Crowley, Valerie M.
Bancells, Cristina
Mira-Martínez, Sofía
Ribas de Pouplana, Lluís
Cortés, Alfred
author_sort Rovira-Graells, Núria
collection PubMed
description The product of the Plasmodium falciparum genes clag3.1 and clag3.2 plays a fundamental role in malaria parasite biology by determining solute transport into infected erythrocytes. Expression of the two clag3 genes is mutually exclusive, such that a single parasite expresses only one of the two genes at a time. Here we investigated the properties and mechanisms of clag3 mutual exclusion using transgenic parasite lines with extra copies of clag3 promoters located either in stable episomes or integrated in the parasite genome. We found that the additional clag3 promoters in these transgenic lines are silenced by default, but under strong selective pressure parasites with more than one clag3 promoter simultaneously active are observed, demonstrating that clag3 mutual exclusion is strongly favored but it is not strict. We show that silencing of clag3 genes is associated with the repressive histone mark H3K9me3 even in parasites with unusual clag3 expression patterns, and we provide direct evidence for heterochromatin spreading in P. falciparum. We also found that expression of a neighbor ncRNA correlates with clag3.1 expression. Altogether, our results reveal a scenario where fitness costs and non-deterministic molecular processes that favor mutual exclusion shape the expression patterns of this important gene family.
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spelling pubmed-47878292016-03-14 Deciphering the principles that govern mutually exclusive expression of Plasmodium falciparum clag3 genes Rovira-Graells, Núria Crowley, Valerie M. Bancells, Cristina Mira-Martínez, Sofía Ribas de Pouplana, Lluís Cortés, Alfred Nucleic Acids Res Gene regulation, Chromatin and Epigenetics The product of the Plasmodium falciparum genes clag3.1 and clag3.2 plays a fundamental role in malaria parasite biology by determining solute transport into infected erythrocytes. Expression of the two clag3 genes is mutually exclusive, such that a single parasite expresses only one of the two genes at a time. Here we investigated the properties and mechanisms of clag3 mutual exclusion using transgenic parasite lines with extra copies of clag3 promoters located either in stable episomes or integrated in the parasite genome. We found that the additional clag3 promoters in these transgenic lines are silenced by default, but under strong selective pressure parasites with more than one clag3 promoter simultaneously active are observed, demonstrating that clag3 mutual exclusion is strongly favored but it is not strict. We show that silencing of clag3 genes is associated with the repressive histone mark H3K9me3 even in parasites with unusual clag3 expression patterns, and we provide direct evidence for heterochromatin spreading in P. falciparum. We also found that expression of a neighbor ncRNA correlates with clag3.1 expression. Altogether, our results reveal a scenario where fitness costs and non-deterministic molecular processes that favor mutual exclusion shape the expression patterns of this important gene family. Oxford University Press 2015-09-30 2015-07-21 /pmc/articles/PMC4787829/ /pubmed/26202963 http://dx.doi.org/10.1093/nar/gkv730 Text en © The Author(s) 2015. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/), which permits non-commercial reuse, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Gene regulation, Chromatin and Epigenetics
Rovira-Graells, Núria
Crowley, Valerie M.
Bancells, Cristina
Mira-Martínez, Sofía
Ribas de Pouplana, Lluís
Cortés, Alfred
Deciphering the principles that govern mutually exclusive expression of Plasmodium falciparum clag3 genes
title Deciphering the principles that govern mutually exclusive expression of Plasmodium falciparum clag3 genes
title_full Deciphering the principles that govern mutually exclusive expression of Plasmodium falciparum clag3 genes
title_fullStr Deciphering the principles that govern mutually exclusive expression of Plasmodium falciparum clag3 genes
title_full_unstemmed Deciphering the principles that govern mutually exclusive expression of Plasmodium falciparum clag3 genes
title_short Deciphering the principles that govern mutually exclusive expression of Plasmodium falciparum clag3 genes
title_sort deciphering the principles that govern mutually exclusive expression of plasmodium falciparum clag3 genes
topic Gene regulation, Chromatin and Epigenetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4787829/
https://www.ncbi.nlm.nih.gov/pubmed/26202963
http://dx.doi.org/10.1093/nar/gkv730
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