Evidence map›Paper›PMID 24088599›Full record

ArticleFly

piRNAs and epigenetic conversion in Drosophila.

Augustin de Vanssay, Anne-Laure Bougé, Antoine Boivin, Catherine Hermant, Laure Teysset, Valérie Delmarre, Christophe Antoniewski, Stéphane Ronsseray

Open access · bronzeAbstract read
In one paragraph

Article in Fly. 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
2.8field-weighted citation impact, top 9% 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

3 citing papers in PubMed, 11 citations in OpenAlex.

  1. Review
  2. Article
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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

8 authors at 4 institutions in 1 country.

Augustin de VanssayEpigenetic Repression and Mobile DNA; Laboratoire Biologie du Développement; UMR7622; CNRS-Université Pierre et Marie Curie; Paris, France.
Anne-Laure BougéDrosophila Genetics and Epigenetics; CNRS URA2578; Institut Pasteur; Paris, France.
Antoine BoivinEpigenetic Repression and Mobile DNA; Laboratoire Biologie du Développement; UMR7622; CNRS-Université Pierre et Marie Curie; Paris, France.
Catherine HermantEpigenetic Repression and Mobile DNA; Laboratoire Biologie du Développement; UMR7622; CNRS-Université Pierre et Marie Curie; Paris, France.
Laure TeyssetEpigenetic Repression and Mobile DNA; Laboratoire Biologie du Développement; UMR7622; CNRS-Université Pierre et Marie Curie; Paris, France.
Valérie DelmarreEpigenetic Repression and Mobile DNA; Laboratoire Biologie du Développement; UMR7622; CNRS-Université Pierre et Marie Curie; Paris, France.
Christophe AntoniewskiDrosophila Genetics and Epigenetics; CNRS URA2578; Institut Pasteur; Paris, France.
Stéphane RonsserayEpigenetic Repression and Mobile DNA; Laboratoire Biologie du Développement; UMR7622; CNRS-Université Pierre et Marie Curie; Paris, France.
Sorbonne Université · FRBipar · FRCentre National de la Recherche Scientifique · FRInstitut Pasteur · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Transposable element (TE) activity is repressed in the Drosophila germline by Piwi-Interacting RNAs (piRNAs), a class of small non-coding RNAs. These piRNAs are produced by discrete genomic loci containing TE fragments. In a recent publication, we tested for the existence of a strict epigenetic induction of piRNA production capacity by a locus in the D. melanogaster genome. We used 2 lines carrying a transgenic 7-copy tandem cluster (P-lacZ-white) at the same genomic site. This cluster generates in both lines a local heterochromatic sector. One line (T-1) produces high levels of ovarian piRNAs homologous to the P-lacZ-white transgenes and shows a strong capacity to repress homologous sequences in trans, whereas the other line (BX2) is devoid of both of these capacities. The properties of these 2 lines are perfectly stable over generations. We have shown that the maternal transmission of a cytoplasm carrying piRNAs from the first line can confer to the inert transgenic locus of the second, a totally de novo capacity to produce high levels of piRNAs as well as the ability to induce homology-dependent silencing in trans. These new properties are stably inherited over generations (n>50). Furthermore, the converted locus has itself become able to convert an inert transgenic locus via cytoplasmic maternal inheritance. This results in a stable epigenetic conversion process, which can be performed recurrently--a phenomenon termed paramutation and discovered in Maize 60 y ago. Paramutation in Drosophila corresponds to the first stable paramutation in animals and provides a model system to investigate the epigenetically induced emergence of a piRNA-producing locus, a crucial step in epigenome shaping. In this Extra View, we discuss some additional functional aspects and the possible molecular mechanism of this piRNA-linked paramutation.

Indexed as

Epigenesis, GeneticAnimalsCytoplasmDrosophila melanogasterFemaleGene Expression RegulationGenome, InsectMaleRNA, Small InterferingRNA, Small Interferingcellular memoryepigeneticsheterochromatinpiRNAstransposable elements

Identifiers

PMID24088599
PMCPMC3896495
OpenAlexW2140851772

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.