Evidence map›Paper›PMID 24068954›Full record

ArticlePLoS genetics2013

Maternal depletion of Piwi, a component of the RNAi system, impacts heterochromatin formation in Drosophila.

Tingting Gu, Sarah C R Elgin

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
14.3field-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

46 citing papers in PubMed, 88 citations in OpenAlex.

  1. Article
  2. Heterochromatin-based silencing of a foreign tandem repeat inbioRxiv : the preprint server for biology · 2025
    Article
  3. Article
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  8. The emerging H3K9me3 chromatin landscape during zebrafish embryogenesis.bioRxiv : the preprint server for biology · 2024
    Article
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  13. Review
  14. Live analysis of position-effect variegation inProceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  15. Article
  16. Article
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  18. Article
  19. Distinct Regulation of the Expression of Satellite DNAs in the BeetleInternational journal of molecular sciences · 2020
    Article
  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

2 authors at 1 institution in 1 country.

Tingting GuDepartment of Biology, Washington University, Saint Louis, Missouri, United States of America.
Sarah C R Elgin
Washington University in St. Louis · US

Funding

Drosophila Transgenic RNAi Resource ProjectR01GM084947 · NIGMS · HARVARD MEDICAL SCHOOL · PI PERRIMON, NORBERT · 2008 to 2019
$9.8M
Formation, Structure and Function in HeterochromatinR01GM068388 · NIGMS · WASHINGTON UNIVERSITY · PI ELGIN, SARAH C.R. · 2003 to 2011
$3.9M
NIGMS NIH HHS R01 GM068388NIGMS NIH HHS R01GM068388NIGMS NIH HHS R01 GM084947
6 · The paper itself

Abstract

A persistent question in epigenetics is how heterochromatin is targeted for assembly at specific domains, and how that chromatin state is faithfully transmitted. Stable heterochromatin is necessary to silence transposable elements (TEs) and maintain genome integrity. Both the RNAi system and heterochromatin components HP1 (Swi6) and H3K9me2/3 are required for initial establishment of heterochromatin structures in S. pombe. Here we utilize both loss of function alleles and the newly developed Drosophila melanogaster transgenic shRNA lines to deplete proteins of interest at specific development stages to dissect their roles in heterochromatin assembly in early zygotes and in maintenance of the silencing chromatin state during development. Using reporters subject to Position Effect Variegation (PEV), we find that depletion of key proteins in the early embryo can lead to loss of silencing assayed at adult stages. The piRNA component Piwi is required in the early embryo for reporter silencing in non-gonadal somatic cells, but knock-down during larval stages has no impact. This implies that Piwi is involved in targeting HP1a when heterochromatin is established at the late blastoderm stage and possibly also during embryogenesis, but that the silent chromatin state created is transmitted through cell division independent of the piRNA system. In contrast, heterochromatin structural protein HP1a is required for both initial heterochromatin assembly and the following mitotic inheritance. HP1a profiles in piwi mutant animals confirm that Piwi depletion leads to decreased HP1a levels in pericentric heterochromatin, particularly in TEs. The results suggest that the major role of the piRNA system in assembly of heterochromatin in non-gonadal somatic cells occurs in the early embryo during heterochromatin formation, and further demonstrate that failure of heterochromatin formation in the early embryo impacts the phenotype of the adult.

Indexed as

Epigenesis, GeneticRNA InterferenceAllelesAnimalsAnimals, Genetically ModifiedArgonaute ProteinsBlastodermChromatinChromosomal Position EffectsChromosomal Proteins, Non-HistoneDNA Transposable ElementsDrosophila melanogasterDrosophila ProteinsEmbryonic DevelopmentEmbryo, NonmammalianGene SilencingArgonaute ProteinsChromatinChromosomal Proteins, Non-HistoneDNA Transposable ElementsDrosophila ProteinsHeterochromatinheterochromatin protein 1, DrosophilaHistone Demethylasespiwi protein, Drosophila

Identifiers

PMID24068954
PMCPMC3777992
OpenAlexW2034572679

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.