Feeding exogenous dsRNA interferes with endogenous sRNA accumulation in Paramecium

Author:

Karunanithi Sivarajan123ORCID,Oruganti Vidya1,de Wijn Raphael4,Drews Franziska5,Cheaib Miriam4,Nordström Karl6,Simon Martin45,Schulz Marcel H13

Affiliation:

1. Cluster of Excellence for Multimodal Computing and Interaction, and Department for Computational Biology & Applied Algorithms, Max Planck Institute for Informatics, Saarland Informatics Campus, Saarbrücken, Germany

2. Graduate School of Computer Science, Saarland Informatics Campus, Saarland University, Saarbrücken, Germany

3. Institute for Cardiovascular Regeneration, Goethe University Hospital, Frankfurt am Main, Germany

4. Molecular Cell Dynamics, Centre for Human and Molecular Biology, Saarland University, Saarbrücken, Germany

5. Molecular Cell Biology and Microbiology, Wuppertal University, Wuppertal, Germany

6. Genetics/Epigenetics, Centre for Human and Molecular Biology, Saarland University, Saarbrücken, Germany

Abstract

Abstract Supply of exogenous dsRNA (exo-dsRNA), either by injection or by feeding, is a fast and powerful alternative to classical knockout studies. The biotechnical potential of feeding techniques is evident from the numerous studies focusing on oral administration of dsRNA to control pests and viral infection in crops/animal farming. We aimed to dissect the direct and indirect effects of exo-dsRNA feeding on the endogenous short interfering RNA (endo-siRNA) populations of the free-living ciliate Paramecium. We introduced dsRNA fragments against Dicer1 (DCR1), involved in RNA interference (RNAi) against exo- and few endo-siRNAs, and an RNAi unrelated gene, ND169. Any feeding, even the control dsRNA, diminishes genome wide the accumulation of endo-siRNAs and mRNAs. This cannot be explained by direct off-target effects and suggests mechanistic overlaps of the exo- and endo-RNAi mechanisms. Nevertheless, we observe a stronger down-regulation of mRNAs in DCR1 feeding compared with ND169 knockdown. This is likely due to the direct involvement of DCR1 in endo-siRNA accumulation. We further observed a cis-regulatory effect on mRNAs that overlap with phased endo-siRNAs. This interference of exo-dsRNA with endo-siRNAs warrants further investigations into secondary effects in target species/consumers, risk assessment of dsRNA feeding applications, and environmental pollution with dsRNA.

Funder

German Research Council

DFG

Publisher

Oxford University Press (OUP)

Subject

Genetics,Molecular Biology,General Medicine

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