Evidence map›Paper›PMID 24468295›Full record

ArticleDevelopmental biology2014

INO80-dependent regression of ecdysone-induced transcriptional responses regulates developmental timing in Drosophila.

Sarah D Neuman, Robert J Ihry, Kelly M Gruetzmacher, Arash Bashirullah

Abstract read
In one paragraph

Article in Developmental biology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.7field-weighted citation impact, top 19% 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

13 citing papers in PubMed, 24 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. AtINO80 represses photomorphogenesis by modulating nucleosome density and H2A.Z incorporation in light-related genes.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  6. Ecdysone controlled cell and tissue deletion.Cell death and differentiation · 2020
    Review
  7. Article
  8. The INO80 remodeller in transcription, replication and repair.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2017
    Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. 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

4 authors at 1 institution in 1 country.

Sarah D NeumanDivision of Pharmaceutical Sciences, University of Wisconsin-Madison, Madison, WI 53705-2222, USA; Cellular and Molecular Biology Graduate Program, University of Wisconsin-Madison, Madison, WI 53705, USA.
Robert J IhryDivision of Pharmaceutical Sciences, University of Wisconsin-Madison, Madison, WI 53705-2222, USA; Cellular and Molecular Biology Graduate Program, University of Wisconsin-Madison, Madison, WI 53705, USA.
Kelly M GruetzmacherDivision of Pharmaceutical Sciences, University of Wisconsin-Madison, Madison, WI 53705-2222, USA; College of Agricultural and Life Sciences, University of Wisconsin-Madison, Madison, WI 53705, USA.
Arash BashirullahDivision of Pharmaceutical Sciences, University of Wisconsin-Madison, Madison, WI 53705-2222, USA; Cellular and Molecular Biology Graduate Program, University of Wisconsin-Madison, Madison, WI 53705, USA. Electronic address: bashirullah@wisc.edu.
University of Wisconsin–Madison · US

Funding

Genetic Analysis of Apoptosis during Drosophila DevelopmentR01GM095944 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI BASHIRULLAH, ARASH · 2011 to 2015
$1.4M
NIGMS NIH HHS R01 GM095944NIGMS NIH HHS R01GM095944
6 · The paper itself

Abstract

Sequential pulses of the steroid hormone ecdysone regulate the major developmental transitions in Drosophila, and the duration of each developmental stage is determined by the length of time between ecdysone pulses. Ecdysone regulates biological responses by directly initiating target gene transcription. In turn, these transcriptional responses are known to be self-limiting, with mechanisms in place to ensure regression of hormone-dependent transcription. However, the biological significance of these transcriptional repression mechanisms remains unclear. Here we show that the chromatin remodeling protein INO80 facilitates transcriptional repression of ecdysone-regulated genes during prepupal development. In ino80 mutant animals, inefficient repression of transcriptional responses to the late larval ecdysone pulse delays the onset of the subsequent prepupal ecdysone pulse, resulting in a significantly longer prepupal stage. Conversely, increased expression of ino80 is sufficient to shorten the prepupal stage by increasing the rate of transcriptional repression. Furthermore, we demonstrate that enhancing the rate of regression of the mid-prepupal competence factor βFTZ-F1 is sufficient to determine the timing of head eversion and thus the duration of prepupal development. Although ino80 is conserved from yeast to humans, this study represents the first characterization of a bona fide ino80 mutation in any metazoan, raising the possibility that the functions of ino80 in transcriptional repression and developmental timing are evolutionarily conserved.

Indexed as

AnimalsChromatin Assembly and DisassemblyDNA-Binding ProteinsDrosophila melanogasterDrosophila ProteinsEcdysoneGene Expression Regulation, DevelopmentalGenes, DevelopmentalGenes, RegulatorMetamorphosis, BiologicalMutationReceptors, SteroidTranscription FactorsTranscription, GeneticDNA-Binding ProteinsDrosophila ProteinsEcdysoneINO80 protein, Drosophilanuclear hormone receptor FTZ-F1 beta, DrosophilaReceptors, SteroidTranscription FactorsChromatin remodelerDevelopmental timingEcdysoneTranscriptional repression

Identifiers

PMID24468295
PMCPMC4005881
OpenAlexW1991942902

What OpenQuestion holds

Textmetadata
LicenceTDM
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.