Dicer‐dependent heterochromatic small RNAs in the model diatom species Phaeodactylum tricornutum

Author:

Grypioti Emilia1234ORCID,Richard Hugues45ORCID,Kryovrysanaki Nikoleta12,Jaubert Marianne46,Falciatore Angela46,Verret Frédéric123ORCID,Kalantidis Kriton12

Affiliation:

1. Department of Biology University of Crete PO Box 2208 70013 Heraklion Crete Greece

2. Institute of Molecular Biology and Biotechnology, Foundation for Research and Technology‐Hellas 70013 Heraklion Crete Greece

3. Institute of Marine Biology and Aquaculture Hellenic Center for Marine Research 71500 Gournes Crete Greece

4. Institut de Biologie Paris‐Seine, Laboratory of Computational and Quantitative Biology UMR 7238 Sorbonne Université 75005 Paris France

5. Bioinformatics Unit, Genome Competence Center (MF1) Robert Koch Institute 13353 Berlin Germany

6. Institut de Biologie Physico‐Chimique, Laboratory of Chloroplast Biology and Light Sensing in Microalgae UMR7141 Centre National de la Recherche Scientifique (CNRS) Sorbonne Université 75005 Paris France

Abstract

Summary Diatoms are eukaryotic microalgae responsible for nearly half of the marine productivity. RNA interference (RNAi) is a mechanism of regulation of gene expression mediated by small RNAs (sRNAs) processed by the endoribonuclease Dicer (DCR). To date, the mechanism and physiological role of RNAi in diatoms are unknown. We mined diatom genomes and transcriptomes for key RNAi effectors and retraced their phylogenetic history. We generated DCR knockout lines in the model diatom species Phaeodactylum tricornutum and analyzed their mRNA and sRNA populations, repression‐associated histone marks, and acclimatory response to nitrogen starvation. Diatoms presented a diversification of key RNAi effectors whose distribution across species suggests the presence of distinct RNAi pathways. P. tricornutum DCR was found to process 26–31‐nt‐long double‐stranded sRNAs originating mostly from transposons covered by repression‐associated epigenetic marks. In parallel, P. tricornutum DCR was necessary for the maintenance of the repression‐associated histone marks H3K9me2/3 and H3K27me3. Finally, PtDCR‐KO lines presented a compromised recovery post nitrogen starvation suggesting a role for P. tricornutum DCR in the acclimation to nutrient stress. Our study characterized the molecular function of the single DCR homolog of P. tricornutum suggesting an association between RNAi and heterochromatin maintenance in this model diatom species.

Funder

Agence Nationale de la Recherche

European Molecular Biology Organization

European Regional Development Fund

General Secretariat for Research and Technology

H2020 Marie Skłodowska-Curie Actions

Hellenic Foundation for Research and Innovation

Japan Society for the Promotion of Science

Publisher

Wiley

Subject

Plant Science,Physiology

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