Evidence map›Paper›PMID 25993106›Full record

ArticlePLoS genetics2015

MicroRNA-Dependent Transcriptional Silencing of Transposable Elements in Drosophila Follicle Cells.

Bruno Mugat, Abdou Akkouche, Vincent Serrano, Claudia Armenise, Blaise Li, Christine Brun, Tudor A Fulga, David Van Vactor, Alain Pélisson, Séverine Chambeyron

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
5.7field-weighted citation impact, top 5% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

13 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
  2. EFFICIENT RIBOSOMAL RNA DEPLETION FROMWellcome open research · 2025
    Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Frontiers in genetics · 2019
    Review
  8. Article
  9. dFmr1 Plays Roles in Small RNA Pathways of Drosophila melanogaster.International journal of molecular sciences · 2017
    Review
  10. Article
  11. Article
  12. Article
  13. Review
4 · The record

Corrections and comments

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

10 authors at 3 institutions in 2 countries.

Bruno MugatInstitut de Génétique Humaine, Centre National de la Recherche Scientifique, Montpellier, France.
Abdou AkkoucheInstitut de Génétique Humaine, Centre National de la Recherche Scientifique, Montpellier, France.
Vincent SerranoInstitut de Génétique Humaine, Centre National de la Recherche Scientifique, Montpellier, France.
Claudia ArmeniseInstitut de Génétique Humaine, Centre National de la Recherche Scientifique, Montpellier, France.
Blaise LiInstitut de Génétique Humaine, Centre National de la Recherche Scientifique, Montpellier, France.
Christine BrunInstitut de Génétique Humaine, Centre National de la Recherche Scientifique, Montpellier, France.
Tudor A FulgaDepartment of Cell Biology and Program in Neuroscience, Harvard Medical School, Boston, Massachusetts, United States of America.
David Van VactorDepartment of Cell Biology and Program in Neuroscience, Harvard Medical School, Boston, Massachusetts, United States of America.
Alain PélissonInstitut de Génétique Humaine, Centre National de la Recherche Scientifique, Montpellier, France.
Séverine ChambeyronInstitut de Génétique Humaine, Centre National de la Recherche Scientifique, Montpellier, France.
Institut de Génétique Humaine · FRCentre National de la Recherche Scientifique · FRHarvard University · US

Funding

Regulation of Synapse Morphogenesis in DrosophilaR01NS069695 · NINDS · HARVARD MEDICAL SCHOOL · PI VAN VACTOR, DAVID L. · 2010 to 2018
$3.3M
Medical Research Council G0902418NINDS NIH HHS 1R01NS069695NINDS NIH HHS R01 NS069695
6 · The paper itself

Abstract

RNA interference-related silencing mechanisms concern very diverse and distinct biological processes, from gene regulation (via the microRNA pathway) to defense against molecular parasites (through the small interfering RNA and the Piwi-interacting RNA pathways). Small non-coding RNAs serve as specificity factors that guide effector proteins to ribonucleic acid targets via base-pairing interactions, to achieve transcriptional or post-transcriptional regulation. Because of the small sequence complementarity required for microRNA-dependent post-transcriptional regulation, thousands of microRNA (miRNA) putative targets have been annotated in Drosophila. In Drosophila somatic ovarian cells, genomic parasites, such as transposable elements (TEs), are transcriptionally repressed by chromatin changes induced by Piwi-interacting RNAs (piRNAs) that prevent them from invading the germinal genome. Here we show, for the first time, that a functional miRNA pathway is required for the piRNA-mediated transcriptional silencing of TEs in this tissue. Global miRNA depletion, caused by tissue- and stage-specific knock down of drosha (involved in miRNA biogenesis), AGO1 or gawky (both responsible for miRNA activity), resulted in loss of TE-derived piRNAs and chromatin-mediated transcriptional de-silencing of TEs. This specific TE de-repression was also observed upon individual titration (by expression of the complementary miRNA sponge) of two miRNAs (miR-14 and miR-34) as well as in a miR-14 loss-of-function mutant background. Interestingly, the miRNA defects differentially affected TE- and 3' UTR-derived piRNAs. To our knowledge, this is the first indication of possible differences in the biogenesis or stability of TE- and 3' UTR-derived piRNAs. This work is one of the examples of detectable phenotypes caused by loss of individual miRNAs in Drosophila and the first genetic evidence that miRNAs have a role in the maintenance of genome stability via piRNA-mediated TE repression.

Indexed as

DNA Transposable ElementsRNA InterferenceAnimalsDrosophilaDrosophila ProteinsFemaleGene Expression RegulationGene SilencingMicroRNAsOvarian FollicleRNA, Small InterferingDNA Transposable ElementsDrosophila ProteinsMicroRNAsMIRN14 microRNA, DrosophilaMIRN34 microRNA, DrosophilaRNA, Small Interfering

Identifiers

PMID25993106
PMCPMC4451950
OpenAlexW1838885635

What OpenQuestion holds

Textmetadata
LicenceCC BY
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Registered trials

None linked

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.