Evidence map›Paper›PMID 28355214›Full record

ArticlePloS one2017

A new paramutation-like example at the Delta gene of Drosophila.

Maria Capovilla, Alain Robichon, Minoo Rassoulzadegan

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.5field-weighted citation impact, top 20% 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

4 citing papers in PubMed, 6 citations in OpenAlex.

  1. Review
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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

3 authors at 2 institutions in 1 country.

Maria CapovillaUMR 1355-7254 INRA/Université Côte d'Azur/CNRS, Institut Sophia Agrobiotech, 400 route des Chappes, Sophia Antipolis, France.
Alain RobichonUMR 1355-7254 INRA/Université Côte d'Azur/CNRS, Institut Sophia Agrobiotech, 400 route des Chappes, Sophia Antipolis, France.
Minoo RassoulzadeganUniversité Côte d'Azur, Inserm U1091-CNRS U7277, Nice, France.
Université Côte d'Azur · FRInserm · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The hereditary transmission of a phenotype independent from DNA sequence implies epigenetic effects. Paramutation is a heritable epigenetic phenomenon observed in plants and animals. To investigate paramutation in Drosophila, we used the P{ry+t7.2 = PZ}Dl05151 P-element insertion in the Drosophila melanogaster genome that causes a dominant visible phenotype: the presence of characteristic extra-veins in the fly wings. This extra-vein phenotype presents variable expressivity and incomplete penetrance. The insert is a PZ element located 680 bp upstream from the ATG of the Delta (Dl) gene, encoding the Notch ligand involved in wing vein development, and acts as a null allele. In the G2 offspring from a cross between the heterozygous transgenic stock and wild-type flies, we observed the transmission of the extra-vein phenotype to wild-type flies without the transgene, independently of gender and across many generations. This is a "paramutation-like" example in the fly: the heritable transmission of a phenotypic change not linked to a classical genetic mutation. A "paramutagenic" allele in heterozygotes transmits the phenotype of the heterozygotes to the wild-type allele ("paramutant") in a stable manner through generations. Distinct from paramutation events so far described in Drosophila, here we deal with a dominant effect on a single gene involving variable hereditary signals.

Indexed as

DNA Transposable ElementsEpigenesis, GeneticGene Expression Regulation, DevelopmentalMutagenesis, InsertionalAllelesAnimalsCrosses, GeneticDrosophila melanogasterDrosophila ProteinsFemaleHeterozygoteInheritance PatternsIntracellular Signaling Peptides and ProteinsMaleMembrane ProteinsReceptors, Notchdelta proteinDNA Transposable ElementsDrosophila ProteinsIntracellular Signaling Peptides and ProteinsMembrane ProteinsN protein, DrosophilaReceptors, Notch

Identifiers

PMID28355214
PMCPMC5371283
OpenAlexW2597968341

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.