Evidence map›Paper›PMID 18454196›Full record

ArticlePLoS genetics2008

Drosophila histone deacetylase-3 controls imaginal disc size through suppression of apoptosis.

Changqi C Zhu, Douglas J Bornemann, David Zhitomirsky, Ellen L Miller, Michael B O'Connor, Jeffrey A Simon

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.1field-weighted citation impact, top 24% 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

22 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
  2. Reversible acetylation of Hpo regulates the Hippo pathway.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  3. Article
  4. Article
  5. Article
  6. HDAC3 Knockdown Dysregulates Juvenile Hormone and Apoptosis-Related Genes inInternational journal of molecular sciences · 2022
    Article
  7. Article
  8. Article
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  11. Article
  12. Article
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  15. Article
  16. Article
  17. Article
  18. Histone deacetylase Rpd3 regulates olfactory projection neuron dendrite targeting via the transcription factor Prospero.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2010
    Article
  19. Regulation of Drosophila melanogaster pro-apoptotic gene hid.Apoptosis : an international journal on programmed cell death · 2009
    Review
  20. 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

6 authors at 2 institutions in 1 country.

Changqi C ZhuDepartment of Genetics, Cell Biology and Development, University of Minnesota, Minneapolis, Minnesota, United States of America.
Douglas J Bornemann
David Zhitomirsky
Ellen L Miller
Michael B O'Connor
Jeffrey A Simon
University of Minnesota · USHoward Hughes Medical Institute · US

Funding

TRANSCRIPTIONAL REPRESSION BY POLYCOMB GROUP PRODUCTSR01GM049850 · NIGMS · UNIVERSITY OF MINNESOTA TWIN CITIES · PI SIMON, JEFFREY A · 1996 to 2017
$4.8M
Howard Hughes Medical InstituteNIGMS NIH HHS GM49850NIGMS NIH HHS R01 GM049850
6 · The paper itself

Abstract

Histone deacetylases (HDACs) execute biological regulation through post-translational modification of chromatin and other cellular substrates. In humans, there are eleven HDACs, organized into three distinct subfamilies. This large number of HDACs raises questions about functional overlap and division of labor among paralogs. In vivo roles are simpler to address in Drosophila, where there are only five HDAC family members and only two are implicated in transcriptional control. Of these two, HDAC1 has been characterized genetically, but its most closely related paralog, HDAC3, has not. Here we describe the isolation and phenotypic characterization of hdac3 mutations. We find that both hdac3 and hdac1 mutations are dominant suppressors of position effect variegation, suggesting functional overlap in heterochromatin regulation. However, all five hdac3 loss-of-function alleles are recessive lethal during larval/pupal stages, indicating that HDAC3 is essential on its own for Drosophila development. The mutant larvae display small imaginal discs, which result from abnormally elevated levels of apoptosis. This cell death occurs as a cell-autonomous response to HDAC3 loss and is accompanied by increased expression of the pro-apoptotic gene, hid. In contrast, although HDAC1 mutants also display small imaginal discs, this appears to result from reduced proliferation rather than from elevated apoptosis. The connection between HDAC loss and apoptosis is important since HDAC inhibitors show anticancer activities in animal models through mechanisms involving apoptotic induction. However, the specific HDACs implicated in tumor cell killing have not been identified. Our results indicate that protein deacetylation by HDAC3 plays a key role in suppression of apoptosis in Drosophila imaginal tissue.

Indexed as

AllelesAnimalsApoptosisCell ProliferationDrosophilaDrosophila ProteinsGene SilencingGenes, InsectGenes, LethalGenes, RecessiveHistone Deacetylase 1Histone Deacetylase 3Histone DeacetylasesHumansLarvaMutationDrosophila ProteinsHDAC1 protein, DrosophilaHID protein, DrosophilaHistone Deacetylase 1Histone Deacetylase 3Histone DeacetylasesNeuropeptides

Identifiers

PMID18454196
PMCPMC2265479
OpenAlexW1996694345

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.