4.6 Article

piRNA pathway evolution beyond gonad context: Perspectives from apicomplexa and trypanosomatids

Journal

FRONTIERS IN GENETICS
Volume 14, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fgene.2023.1129194

Keywords

Argonautes (AGO); Toxoplasma; Trypanosoma; PIWI; piRNA biogenesis

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piRNAs function as genome defense mechanisms against transposable elements insertions within germ line cells, and recent studies have revealed their presence in non-gonadal somatic contexts. The presence of piRNA pathways has also been reported in bacteria, mollusks, and arthropods, with various functions including genome protection, gene expression regulation, and axon regeneration. In parasitic protozoa, the presence of PIWI-related machinery suggests the existence of an ancestral piRNA machinery that evolved in multicellular eukaryotes. Understanding current and ancestral PIWI/piRNAs will provide insights into genome integrity conservation and host defense mechanisms by protozoan parasites.
piRNAs function as genome defense mechanisms against transposable elements insertions within germ line cells. Recent studies have unraveled that piRNA pathways are not limited to germ cells as initially reckoned, but are instead also found in non-gonadal somatic contexts. Moreover, these pathways have also been reported in bacteria, mollusks and arthropods, associated with safeguard of genomes against transposable elements, regulation of gene expression and with direct consequences in axon regeneration and memory formation. In this Perspective we draw attention to early branching parasitic protozoa, whose genome preservation is an essential function as in late eukaryotes. However, little is known about the defense mechanisms of these genomes. We and others have described the presence of putative PIWI-related machinery members in protozoan parasites. We have described the presence of a PIWI-like protein in Trypanosoma cruzi, bound to small non-coding RNAs (sRNAs) as cargo of secreted extracellular vesicles relevant in intercellular communication and host infection. Herein, we put forward the presence of members related to Argonaute pathways in both Trypanosoma cruzi and Toxoplasma gondii. The presence of PIWI-like machinery in Trypansomatids and Apicomplexa, respectively, could be evidence of an ancestral piRNA machinery that evolved to become more sophisticated and complex in multicellular eukaryotes. We propose a model in which ancient PIWI proteins were expressed broadly and had functions independent of germline maintenance. A better understanding of current and ancestral PIWI/piRNAs will be relevant to better understand key mechanisms of genome integrity conservation during cell cycle progression and modulation of host defense mechanisms by protozoan parasites.

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