Evidence map›Paper›PMID 24896584›Full record

ArticlePloS one2014

Functional analysis of the Drosophila embryonic germ cell transcriptome by RNA interference.

Ferenc Jankovics, László Henn, Ágnes Bujna, Péter Vilmos, Kerstin Spirohn, Michael Boutros, Miklós Erdélyi

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.6field-weighted citation impact, top 33% 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

8 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Leveraging CRISPR-Cas13d in an inducible knockdown system to interrogatebioRxiv : the preprint server for biology · 2025
    Article
  3. Cells · 2022
    Article
  4. Article
  5. Article
  6. Finding their way: themes in germ cell migration.Current opinion in cell biology · 2016
    Review
  7. Article
  8. 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

7 authors at 3 institutions in 2 countries.

Ferenc JankovicsInstitute of Genetics, Biological Research Centre of the Hungarian Academy of Sciences, Szeged, Hungary.
László HennInstitute of Genetics, Biological Research Centre of the Hungarian Academy of Sciences, Szeged, Hungary.
Ágnes BujnaInstitute of Genetics, Biological Research Centre of the Hungarian Academy of Sciences, Szeged, Hungary.
Péter VilmosInstitute of Genetics, Biological Research Centre of the Hungarian Academy of Sciences, Szeged, Hungary.
Kerstin SpirohnGerman Cancer Research Center (DKFZ) and Heidelberg University, Division Signaling and Functional Genomics, Heidelberg, Germany.
Michael BoutrosGerman Cancer Research Center (DKFZ) and Heidelberg University, Division Signaling and Functional Genomics, Heidelberg, Germany.
Miklós ErdélyiInstitute of Genetics, Biological Research Centre of the Hungarian Academy of Sciences, Szeged, Hungary.
HUN-REN Szegedi Biológiai Kutatóközpont · HUGerman Cancer Research Center · DEHungarian Academy of Sciences · HU

Funding

Howard Hughes Medical Institute 55005606
6 · The paper itself

Abstract

In Drosophila melanogaster, primordial germ cells are specified at the posterior pole of the very early embryo. This process is regulated by the posterior localized germ plasm that contains a large number of RNAs of maternal origin. Transcription in the primordial germ cells is actively down-regulated until germ cell fate is established. Bulk expression of the zygotic genes commences concomitantly with the degradation of the maternal transcripts. Thus, during embryogenesis, maternally provided and zygotically transcribed mRNAs determine germ cell development collectively. In an effort to identify novel genes involved in the regulation of germ cell behavior, we carried out a large-scale RNAi screen targeting both maternal and zygotic components of the embryonic germ line transcriptome. We identified 48 genes necessary for distinct stages in germ cell development. We found pebble and fascetto to be essential for germ cell migration and germ cell division, respectively. Our data uncover a previously unanticipated role of mei-P26 in maintenance of embryonic germ cell fate. We also performed systematic co-RNAi experiments, through which we found a low rate of functional redundancy among homologous gene pairs. As our data indicate a high degree of evolutionary conservation in genetic regulation of germ cell development, they are likely to provide valuable insights into the biology of the germ line in general.

Indexed as

Gene Expression Regulation, DevelopmentalRNA InterferenceTranscriptomeAnimalsCell DivisionCluster AnalysisComputational BiologyDrosophilaDrosophila ProteinsGene Expression ProfilingGene SilencingGerm CellsGuanine Nucleotide Exchange FactorsMitosisPhenotypeReproducibility of ResultsDrosophila ProteinsGuanine Nucleotide Exchange FactorsPbl protein, Drosophila

Identifiers

PMID24896584
PMCPMC4045815
OpenAlexW2077383652

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.