Evidence map›Paper›PMID 29281970›Full record

ArticleBMC genomics2017

Transcriptional effects of a positive feedback circuit in Drosophila melanogaster.

Jarosław Bryk, R Guy Reeves, Floyd A Reed, Jai A Denton

Open access · goldAbstract read
In one paragraph

Article in BMC genomics, 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
0.3field-weighted citation impact, top 38% 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, 8 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Synthetic Mutualism and the Intervention Dilemma.Life (Basel, Switzerland) · 2019
    Review
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

4 authors at 4 institutions in 4 countries.

Jarosław BrykDepartment of Evolutionary Genetics, Max Planck Institute for Evolutionary Biology, Plön, Germany.
R Guy ReevesDepartment of Evolutionary Genetics, Max Planck Institute for Evolutionary Biology, Plön, Germany.
Floyd A ReedDepartment of Evolutionary Genetics, Max Planck Institute for Evolutionary Biology, Plön, Germany.
Jai A DentonDepartment of Evolutionary Genetics, Max Planck Institute for Evolutionary Biology, Plön, Germany. jai.denton@oist.jp.ORCID 0000-0002-5259-4221
Max Planck Institute for Evolutionary Biology · DEOkinawa Institute of Science and Technology Graduate University · JPUniversity of Hawaiʻi at Mānoa · USUniversity of Huddersfield · GB

Funding

Resource Component: Acquisition, maintenance and distribution of Drosophila stocksP40OD018537 · OD · TRUSTEES OF INDIANA UNIVERSITY · PI Annette L. Parks · 2014 to 2026
$13.5M
Deutsche Forschungsgemeinschaft RE-3062/2-1NIH HHS P40 OD018537
6 · The paper itself

Abstract

backgroundSynthetic systems that use positive feedback have been developed to control human disease vectors and crop pests. The tTAV system, which has been deployed in several insect species, relies on a positive feedback circuit that can be inhibited via dietary tetracycline. Although insects carrying tTAV fail to survive until adulthood in the absence of tetracycline, the exact reason for its lethality, as well as the transcriptomic effects of an active positive feedback circuit, remain unknown.

resultsWe engineered the tTAV system in Drosophila melanogaster and investigated the effects of tTAV genome integration locus on the whole fly transcriptome during larval and adult life stages in four transgenic fly strains using gene expression microarrays. We found that while there were widespread effects on the transcriptome, the gene expression differences after removal of tetracycline were not consistent between integration sites. No specific region of the genome was affected, no common set of genes or pathways, nor did the integration site affect the transcripts in cis.

conclusionAlthough the positive feedback tTAV system is effective at killing insect larvae regardless of where it is inserted in the genome, it does not exhibit a specific, consistent transcriptional signature. Instead, each insertion site is associated with broad, but different, transcriptional effects. Our results suggest that lethality may not be caused by a direct effect on transcription of a set of key genes or pathways. Instead, we propose that rather than a specific action of a tTAV protein, it is the stochastic transcriptional effects specific to each insertion site that contribute to the tTAV-induced mortality.

Indexed as

Gene Expression RegulationGenes, SyntheticTranscription, GeneticAnimalsAnimals, Genetically ModifiedDrosophila melanogasterFeedback, PhysiologicalGene Expression ProfilingOligonucleotide Array Sequence AnalysisSpecies SpecificityTranscriptomeDrosophila melanogasterMicroarraysTetracyclineTranscriptometTAVVector control

Identifiers

PMID29281970
PMCPMC5746007
OpenAlexW2781342797

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.