Sir2a regulates rDNA transcription and multiplication rate in the human malaria parasite Plasmodium falciparum

Liliana Mancio-Silva, Jose Juan Lopez-Rubio, Aurélie Claes and Artur Scherf ()
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Liliana Mancio-Silva: Institut Pasteur, Unité de Biologie des Interactions Hôte-Parasite
Jose Juan Lopez-Rubio: Institut Pasteur, Unité de Biologie des Interactions Hôte-Parasite
Aurélie Claes: Institut Pasteur, Unité de Biologie des Interactions Hôte-Parasite
Artur Scherf: Institut Pasteur, Unité de Biologie des Interactions Hôte-Parasite

Nature Communications, 2013, vol. 4, issue 1, 1-6

Abstract: Abstract The Plasmodium falciparum histone deacetylase Sir2a localizes at telomeric regions where it contributes to epigenetic silencing of clonally variant virulence genes. Apart from telomeres, PfSir2a also accumulates in the nucleolus, which harbours the developmentally regulated ribosomal RNA genes. Here we investigate the nucleolar function of PfSir2a and demonstrate that PfSir2a fine-tunes ribosomal RNA gene transcription. Using a parasite line in which PfSir2a has been disrupted, we observe that histones near the transcription start sites of all ribosomal RNA genes are hyperacetylated and that transcription of ribosomal RNA genes is upregulated. Complementation of the PfSir2a-disrupted parasites restores the ribosomal RNA levels, whereas PfSir2a overexpression in wild-type parasites decreases ribosomal RNA synthesis. Furthermore, we observe that PfSir2a modulation of ribosomal RNA synthesis is linked to an altered number of daughter merozoites and the parasite multiplication rate. These findings provide new insights into an epigenetic mechanism that controls malaria parasite proliferation and virulence.

Date: 2013
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DOI: 10.1038/ncomms2539

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