Evidence map›Paper›PMID 38713108›Full record

ArticleGenome biology and evolution2024

The Evolution and Characterization of the RNA Interference Pathways in Lophotrochozoa.

Alessandro Formaggioni, Gianmarco Cavalli, Mayuko Hamada, Tatsuya Sakamoto, Federico Plazzi, Marco Passamonti

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Article in Genome biology and evolution, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. SmithRNAs: A Common Feature among Metazoa.Genome biology and evolution · 2025
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4 · The record

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PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Alessandro FormaggioniDepartment of Biological, Geological and Environmental Sciences, University of Bologna, Bologna, Italy.
Gianmarco CavalliDepartment of Biological, Geological and Environmental Sciences, University of Bologna, Bologna, Italy.
Mayuko HamadaUshimado Marine Institute, Okayama University, Okayama, Japan.
Tatsuya SakamotoUshimado Marine Institute, Okayama University, Okayama, Japan.
Federico PlazziDepartment of Biological, Geological and Environmental Sciences, University of Bologna, Bologna, Italy.ORCID 0000-0001-5920-7557
Marco PassamontiDepartment of Biological, Geological and Environmental Sciences, University of Bologna, Bologna, Italy.ORCID 0000-0002-6222-8225

Funding

Canziani BequestItalian Ministry of University and Research PRIN 2020 2020BE2BC3
6 · The paper itself

Abstract

In animals, three main RNA interference mechanisms have been described so far, which respectively maturate three types of small noncoding RNAs (sncRNAs): miRNAs, piRNAs, and endo-siRNAs. The diversification of these mechanisms is deeply linked with the evolution of the Argonaute gene superfamily since each type of sncRNA is typically loaded by a specific Argonaute homolog. Moreover, other protein families play pivotal roles in the maturation of sncRNAs, like the DICER ribonuclease family, whose DICER1 and DICER2 paralogs maturate respectively miRNAs and endo-siRNAs. Within Metazoa, the distribution of these families has been only studied in major groups, and there are very few data for clades like Lophotrochozoa. Thus, we here inferred the evolutionary history of the animal Argonaute and DICER families including 43 lophotrochozoan species. Phylogenetic analyses along with newly sequenced sncRNA libraries suggested that in all Trochozoa, the proteins related to the endo-siRNA pathway have been lost, a part of them in some phyla (i.e. Nemertea, Bryozoa, Entoprocta), while all of them in all the others. On the contrary, early diverging phyla, Platyhelminthes and Syndermata, showed a complete endo-siRNA pathway. On the other hand, miRNAs were revealed the most conserved and ubiquitous mechanism of the metazoan RNA interference machinery, confirming their pivotal role in animal cell regulation.

Indexed as

Evolution, MolecularMicroRNAsPhylogenyRibonuclease IIIRNA InterferenceAnimalsArgonaute ProteinsInvertebratesRNA, Small InterferingArgonaute ProteinsMicroRNAsRibonuclease IIIRNA, Small InterferingArgonauteDICERLophotrochozoaMetazoaRNAi

Identifiers

PMID38713108
PMCPMC11114477

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.