Abstract

In RNA silencing, small RNAs produced by the RNase-III Dicer guide Argonaute-like proteins as part of RNA-induced silencing complexes (RISC) to regulate gene expression transcriptionally or post-transcriptionally. Here, we have characterized the RNA silencing machinery and exhaustive small RNAome of Toxoplasma gondii, member of the Apicomplexa, a phylum of animal- and human-infecting parasites that cause extensive health and economic damages to human populations worldwide. Remarkably, the small RNA-generating machinery of Toxoplasma is phylogenetically and functionally related to that of plants and fungi, and accounts for an exceptionally diverse array of small RNAs. This array includes conspicuous populations of repeat-associated small interfering RNA (siRNA), which, as in plants, likely generate and maintain heterochromatin at DNA repeats and satellites. Toxoplasma small RNAs also include many microRNAs with clear metazoan-like features whose accumulation is sometimes extremely high and dynamic, an unexpected finding given that Toxoplasma is a unicellular protist. Both plant-like heterochromatic small RNAs and metazoan-like microRNAs bind to a single Argonaute protein, Tg-AGO. Toxoplasma miRNAs co-sediment with polyribosomes, and thus, are likely to act as translational regulators, consistent with the lack of catalytic residues in Tg-AGO. Mass spectrometric analyses of the Tg-AGO protein complex revealed a common set of virtually all known RISC components so far characterized in human and Drosophila, as well as novel proteins involved in RNA metabolism. In agreement with its loading with heterochromatic small RNAs, Tg-AGO also associates substoichiometrically with components of known chromatin-repressing complexes. Thus, a puzzling patchwork of silencing processor and effector proteins from plant, fungal and metazoan origin accounts for the production and action of an unsuspected variety of small RNAs in the single-cell parasite Toxoplasma and possibly in other apicomplexans. This study establishes Toxoplasma as a unique model system for studying the evolution and molecular mechanisms of RNA silencing among eukaryotes.

Highlights

  • Apicomplexa are unicellular eukaryotes that multiply intracellularly in their mammalian hosts

  • To test the possibility of target cleavage and degradation mediated by Tg-AGO, we examined the levels of mRNA predicted as strong targets of isotype-specific Tg-miRNAs (Table S2)

  • HAFlag-Tg-AGO was found to co-purify with Tg-PRMT1, which belongs to the family of arginine methyltransferases that use RGG motifs as substrates (Table 1). These results suggest that Tg-AGO is arginine-methylated, and that this modification might be read by Tg-Tudor/SN, possibly to engage Tg-AGO into distinct modes of RNA silencing

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Summary

Introduction

Apicomplexa are unicellular eukaryotes that multiply intracellularly in their mammalian hosts They include parasites of major medical importance like Plasmodium species, the causative agent of malaria, and Toxoplasma gondii, the most widespread apicomplexan parasite, present virtually everywhere on earth. Changes in gene expression is expected as (i) parasites progress through the cell cycle, (ii) parasites differentiate in specific stages, and (iii) parasites are exposed to the host immune system during infection [4]. How these changes are regulated at the molecular level remains to a large extent unknown. Despite the paucity of recognizable TFs, apicomplexans are endowed with a rich repertoire of enzymes associated with epigenetics and chromatin remodeling, and this observation has

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