Evidence map›Paper›PMID 26276385›Full record

ArticleG3 (Bethesda, Md.)2015

A Flippase-Mediated GAL80/GAL4 Intersectional Resource for Dissecting Appendage Development in Drosophila.

Brittany N Smith, Arash M Ghazanfari, Rudolf A Bohm, William P Welch, Bing Zhang, John P Masly

Open access · goldAbstract read
In one paragraph

Article in G3 (Bethesda, Md.), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact, top 96% 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

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Article
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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

6 authors at 3 institutions in 1 country.

Brittany N SmithDepartment of Biology, University of Oklahoma, Norman, Oklahoma 73019.
Arash M GhazanfariDepartment of Biology, University of Oklahoma, Norman, Oklahoma 73019.
Rudolf A BohmDepartment of Biology, University of Oklahoma, Norman, Oklahoma 73019 Department of Biological and Health Sciences, Texas A&M University, Kingsville, Texas 78363.
William P WelchDepartment of Biology, University of Oklahoma, Norman, Oklahoma 73019.
Bing ZhangDepartment of Biology, University of Oklahoma, Norman, Oklahoma 73019 Division of Biological Sciences, University of Missouri, Columbia, Missouri 65211.
John P MaslyDepartment of Biology, University of Oklahoma, Norman, Oklahoma 73019 masly@ou.edu.ORCID http://orcid.org/0000-0003-3448-0914
University of Oklahoma · USTexas A&M University – Kingsville · USUniversity of Missouri · US

Funding

Resource Component: Acquisition, maintenance and distribution of Drosophila stocksP40OD018537 · OD · TRUSTEES OF INDIANA UNIVERSITY · PI Annette L. Parks · 2014 to 2026
$13.5M
Drosophila Transgenic RNAi Resource ProjectR01GM084947 · NIGMS · HARVARD MEDICAL SCHOOL · PI PERRIMON, NORBERT · 2008 to 2019
$9.8M
Novel Genetic Approaches to Evaluate Dominant Gain of Function Toxicity in PolyglSC2NS091009 · NINDS · TEXAS A&M UNIVERSITY-KINGSVILLE · PI BOHM, RUDOLF · 2014 to 2016
$404k
NIGMS NIH HHS R01 GM084947NIGMS NIH HHS R01-GM084947NIH HHS P40 OD018537NIH HHS P40-OD018537NINDS NIH HHS 1SC2NS091009-01NINDS NIH HHS SC2 NS091009
6 · The paper itself

Abstract

Drosophila imaginal discs provide an ideal model to study processes important for cell signaling and cell specification, tissue differentiation, and cell competition during development. One challenge to understanding genetic control of cellular processes and cell interactions is the difficulty in effectively targeting a defined subset of cells in developing tissues in gene manipulation experiments. A recently developed Flippase-induced intersectional GAL80/GAL4 repression method incorporates several gene manipulation technologies in Drosophila to enable such fine-scale dissection in neural tissues. In particular, this approach brings together existing GAL4 transgenes, newly developed enhancer-trap flippase transgenes, and GAL80 transgenes flanked by Flippase recognition target sites. The combination of these tools enables gene activation/repression in particular subsets of cells within a GAL4 expression pattern. Here, we expand the utility of a large collection of these enhancer-trap flippase transgenic insertion lines by characterizing their expression patterns in third larval instar imaginal discs. We screened 521 different enhancer-trap flippase lines and identified 28 that are expressed in imaginal tissues, including two transgenes that show sex-specific expression patterns. Using a line that expresses Flippase in the wing imaginal disc, we demonstrate the utility of this intersectional approach for studying development by knocking down gene expression of a key member of the planar cell polarity pathway. The results of our experiments show that these enhancer-trap flippase lines enable fine-scale manipulation in imaginal discs.

Indexed as

Gene Expression RegulationAnimalsDrosophilaDrosophila ProteinsGene ExpressionImaginal DiscsLarvaRecombination, GeneticRepressor ProteinsTranscription FactorsDrosophila ProteinsGAL4 protein, DrosophilaRepressor ProteinsTranscription FactorsDrosophilaenhancer-trap Flippasegenetic manipulationimaginal discs

Identifiers

PMID26276385
PMCPMC4592993
OpenAlexW1842100747

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.