from 28 settembre 2026 to 2 ottobre 2026
Department of Agricultural Sciences of the University of Napoli Federico II, Portici, Italy
Europe/Rome timezone

Small RNA biogenesis in Duckweeds

29 set 2026, 17:55
20m
Sala Monumentini ()

Sala Monumentini

Piazza Carlo di Borbone I, Portici

Speaker

Mr. Filipp Krasnovid (Gregor Mendel institute, Vienna Biocenter PhD Programm)

Description

Small RNA silencing pathways in plants play crucial roles in development, antiviral resistance, and transposon control. There are two types of silencing: transcriptional gene silencing (TGS) and post-transcriptional (PTGS). TGS acts via the RNA-directed DNA methylation pathway and 24nt-long small interfering RNAs (siRNAs). PTGS functions at the mRNA level, where viral or transgene RNA transcripts trigger the formation of 21nt- and 22nt-long siRNAs that target AGO proteins toward these transcripts leading to their cleavage and degradation.

Duckweeds have simplified their silencing pathways and challenge the current model of PTGS in several ways. Dicer-like protein 2 (DCL2), the protein responsible for the production of 22nt siRNA, conserved among plants, is lost in duckweeds, yet we observe 22nt siRNA in all three species studied in our lab. Transgenic silencing in Lemna minor is characterised by the equal presence of both 21nt- and 22nt-long siRNAs; transient expression of an inverted repeat (IR) in Spirodela polyrhiza and in Wolffia brasiliensis results in the production of both 21nt and 22nt siRNA derived from this IR. These 22nt siRNAs, in turn, do not seem to trigger transitivity, the silencing amplification process, despite the presence of all the necessary elements that we know of.

The goal of our project is to understand the biogenesis of 22nt-long siRNA and find the mechanisms responsible for the difference in PTGS functioning in duckweeds, including transitivity — a phenomenon that is not well understood even in conventional models such as Arabidopsis.

Keywords

small RNA, PTGS, silencing

References

Barragan-Borrero V, de Santana Lopes A, Rodrigues-Batista ED, et al. (2026) Strain, procedures, and tools for reproducible genetic transformation and genome editing of the emerging plant model Spirodela polyrhiza New Phytol 250(2):735-56 preprint bioRxiv:2025.08.28.672806

Dombey R, Buendía-Ávila D, ..., Marí-Ordóñez A (2025) Atypical epigenetic and small RNA control of degenerated transposons and their fragments in clonally reproducing Spirodela polyrhiza. Genome Res 35(3):522-44 preprint bioRxiv: 2024.04.03.587901

Buendia-Avila D, Barragan-Borrero V, ..., Mari-Ordonez A (2026) Transposon expansion is associated with reorganization of small RNA and DNA methylation landscapes in the morphologically minimal angiosperm Wolffia brasiliensis. bioRxiv:2026.02.27.708460

Primary author

Mr. Filipp Krasnovid (Gregor Mendel institute, Vienna Biocenter PhD Programm)

Co-authors

Dr. Veronica Barragan-Borrero (Gregor Mendel Institute) Mr. Arturo Ponce (Gregor Mendel Institute) Dr. Laura Diezma-Navas (Gregor Mendel Institute) Dr. Daniel Buendia (Gregor Mendel Institute) Dr. Arturo Marí-Ordóñez (Gregor Mendel Institute)

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