Evidence map›Paper›PMID 27527791›Full record

ArticleG3 (Bethesda, Md.)2016

Potential Direct Regulators of the Drosophila yellow Gene Identified by Yeast One-Hybrid and RNAi Screens.

Gizem Kalay, Richard Lusk, Mackenzie Dome, Korneel Hens, Bart Deplancke, Patricia J Wittkopp

Open access · goldAbstract read
In one paragraph

Article in G3 (Bethesda, Md.), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.5field-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

12 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
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  8. TheeLife · 2019
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  9. Article
  10. Review
  11. Article
  12. 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

6 authors at 2 institutions in 2 countries.

Gizem KalayDepartment of Molecular, Cellular, and Developmental Biology, University of Michigan, Ann Arbor, Michigan 48109.
Richard LuskDepartment of Ecology and Evolutionary Biology, University of Michigan, Ann Arbor, Michigan 48109.
Mackenzie DomeDepartment of Molecular, Cellular, and Developmental Biology, University of Michigan, Ann Arbor, Michigan 48109.
Korneel HensInstitute of Bioengineering, School of Life Sciences, Ecole Polytechnique Fédéral de Lausanne, CH-1015 Lausanne, Switzerland.
Bart DeplanckeInstitute of Bioengineering, School of Life Sciences, Ecole Polytechnique Fédéral de Lausanne, CH-1015 Lausanne, Switzerland.
Patricia J WittkoppDepartment of Molecular, Cellular, and Developmental Biology, University of Michigan, Ann Arbor, Michigan 48109 Department of Ecology and Evolutionary Biology, University of Michigan, Ann Arbor, Michigan 48109 wittkopp@umich.edu.
University of Michigan–Ann Arbor · USÉcole Polytechnique Fédérale de Lausanne · CH

Funding

Evolutionary Genetics: Contribution of Tan to Drosophila Pigmentation DivergenceR01GM089736 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI WITTKOPP, PATRICIA JEAN · 2010 to 2014
$1.3M
NIGMS NIH HHS R01 GM089736
6 · The paper itself

Abstract

The regulation of gene expression controls development, and changes in this regulation often contribute to phenotypic evolution. Drosophila pigmentation is a model system for studying evolutionary changes in gene regulation, with differences in expression of pigmentation genes such as yellow that correlate with divergent pigment patterns among species shown to be caused by changes in cis- and trans-regulation. Currently, much more is known about the cis-regulatory component of divergent yellow expression than the trans-regulatory component, in part because very few trans-acting regulators of yellow expression have been identified. This study aims to improve our understanding of the trans-acting control of yellow expression by combining yeast-one-hybrid and RNAi screens for transcription factors binding to yellow cis-regulatory sequences and affecting abdominal pigmentation in adults, respectively. Of the 670 transcription factors included in the yeast-one-hybrid screen, 45 showed evidence of binding to one or more sequence fragments tested from the 5' intergenic and intronic yellow sequences from D. melanogaster, D. pseudoobscura, and D. willistoni, suggesting that they might be direct regulators of yellow expression. Of the 670 transcription factors included in the yeast-one-hybrid screen, plus another TF previously shown to be genetically upstream of yellow, 125 were also tested using RNAi, and 32 showed altered abdominal pigmentation. Nine transcription factors were identified in both screens, including four nuclear receptors related to ecdysone signaling (Hr78, Hr38, Hr46, and Eip78C). This finding suggests that yellow expression might be directly controlled by nuclear receptors influenced by ecdysone during early pupal development when adult pigmentation is forming.

Indexed as

Gene Expression RegulationGenetic Association StudiesRNA InterferenceTwo-Hybrid System TechniquesAnimalsDrosophilaDrosophila ProteinsEcdysoneEnhancer Elements, GeneticGenetic TestingMutationPhenotypePigmentationProtein BindingTranscription FactorsDrosophila ProteinsEcdysoneTranscription FactorsecdysoneHr38Hr78Mutant Screen Reportpigmentationtranscription factor

Identifiers

PMID27527791
PMCPMC5068961
OpenAlexW2512572631

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.