Evidence map›Paper›PMID 24782529›Full record

ArticleNucleic acids research2014

Impact of nuclear Piwi elimination on chromatin state in Drosophila melanogaster ovaries.

Mikhail S Klenov, Sergey A Lavrov, Alina P Korbut, Anastasia D Stolyarenko, Evgeny Y Yakushev, Michael Reuter, Ramesh S Pillai, Vladimir A Gvozdev

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
13.5field-weighted citation impact, top 1% 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

48 citing papers in PubMed, 85 citations in OpenAlex.

  1. Article
  2. Review
  3. Paramutation-Like Behavior of Genic piRNA-Producing Loci inInternational journal of molecular sciences · 2025
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  18. Article
  19. RNA matchmaking in chromatin regulation.Biochemical Society transactions · 2020
    Review
  20. Article
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 3 institutions in 2 countries.

Mikhail S KlenovInstitute of Molecular Genetics, Russian Academy of Sciences, Moscow 123182, Russia.
Sergey A LavrovInstitute of Molecular Genetics, Russian Academy of Sciences, Moscow 123182, Russia.
Alina P KorbutInstitute of Molecular Genetics, Russian Academy of Sciences, Moscow 123182, Russia.
Anastasia D StolyarenkoInstitute of Molecular Genetics, Russian Academy of Sciences, Moscow 123182, Russia.
Evgeny Y YakushevInstitute of Molecular Genetics, Russian Academy of Sciences, Moscow 123182, Russia.
Michael ReuterEuropean Molecular Biology Laboratory, Grenoble Outstation, 71 avenue des Martyrs, 38042 France Unit for Virus Host-Cell Interactions, University of Grenoble Alpes-EMBL-CNRS, 71 avenue des Martyrs, 38042 France.
Ramesh S PillaiEuropean Molecular Biology Laboratory, Grenoble Outstation, 71 avenue des Martyrs, 38042 France Unit for Virus Host-Cell Interactions, University of Grenoble Alpes-EMBL-CNRS, 71 avenue des Martyrs, 38042 France.
Vladimir A GvozdevInstitute of Molecular Genetics, Russian Academy of Sciences, Moscow 123182, Russia gvozdev@img.ras.ru.
Institute of Molecular Genetics · RUUnit of Virus Host Cell Interactions · FRUniversité Grenoble Alpes · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The Piwi-interacting RNA (piRNA)-interacting Piwi protein is involved in transcriptional silencing of transposable elements in ovaries of Drosophila melanogaster. Here we characterized the genome-wide effect of nuclear Piwi elimination on the presence of the heterochromatic H3K9me3 mark and HP1a, as well as on the transcription-associated mark H3K4me2. Our results demonstrate that a significant increase in the H3K4me2 level upon nuclear Piwi loss is not accompanied by the alterations in H3K9me3 and HP1a levels for several germline-expressed transposons, suggesting that in this case Piwi prevents transcription by a mechanism distinct from H3K9 methylation. We found that the targets of Piwi-dependent chromatin repression are mainly related to the elements that display a higher level of H3K4me2 modification in the absence of silencing, i.e. most actively transcribed elements. We also show that Piwi-guided silencing does not significantly influence the chromatin state of dual-strand piRNA-producing clusters. In addition, host protein-coding gene expression is essentially not affected due to the nuclear Piwi elimination, but we noted an increase in small nuclear spliceosomal RNAs abundance and propose Piwi involvement in their post-transcriptional regulation. Our work reveals new aspects of transposon silencing in Drosophila, indicating that transcription of transposons can underpin their Piwi dependent silencing, while canonical heterochromatin marks are not obligatory for their repression.

Indexed as

Gene SilencingAnimalsArgonaute ProteinsCell NucleusChromatinChromobox Protein Homolog 5Chromosomal Proteins, Non-HistoneDrosophila melanogasterDrosophila ProteinsFemaleHistonesOvaryRetroelementsRNA, Small NuclearArgonaute ProteinsChromatinChromobox Protein Homolog 5Chromosomal Proteins, Non-HistoneDrosophila ProteinsHistonespiwi protein, DrosophilaRetroelementsRNA, Small Nuclear

Identifiers

PMID24782529
PMCPMC4041442
OpenAlexW2120930276

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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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.